Kandel, et.al.; Principles of Neural Science
Book Page   Topic    
Kandel; Principles of Neural Science 5 Brain and behavior
Kandel; Principles of Neural Science 12 Brodmann's areas (diagram) 7
Kandel; Principles of Neural Science 19 Nerve cells and behavior 7
Kandel; Principles of Neural Science 23 Branches of a single axon may form synapses with as many as 1000 other neurons. 4
Kandel; Principles of Neural Science 36 Genes and behavior 13
Kandel; Principles of Neural Science 67 Cytology of neurons 31
Kandel; Principles of Neural Science 88 Synthesis and trafficking of neuronal protein 21
Kandel; Principles of Neural Science 105 Ion channels 17
Kandel; Principles of Neural Science 125 Membrane potential 20
Kandel; Principles of Neural Science 140 Local signaling: Passive electrical properties of the Neuron 15
Kandel; Principles of Neural Science 150 Propagated signaling: Action Potential 10
Kandel; Principles of Neural Science 175 Overview of Synaptic Transmission 25
Kandel; Principles of Neural Science 187 Signaling at the nerve muscle synapse: Directly-Gated Transmission 12
Kandel; Principles of Neural Science 207 Synaptic Integration 20
Kandel; Principles of Neural Science 207 Muscle fibers receive only excitatory, while central neurons receive both excitatory and inhibitory inputs. 0
Kandel; Principles of Neural Science 207 All semantic actions on muscle fibers are mediated by one neurotransmitter, acetylcholine (Ach) 0
Kandel; Principles of Neural Science 207 In the central nervous system the inputs to a single cell are mediated by variety of transmitters that alter the activity of a variety of ion channels. 0
Kandel; Principles of Neural Science 207 CNS neuron ion channels include many that are directly gated by transmitters, but others that are gated indirectly by metabotropic receptors and the second messengers they activate. 0
Kandel; Principles of Neural Science 207 CNS neurons must integrate diverse inputs into one coordinated response. 0
Kandel; Principles of Neural Science 207 Nerve muscle synapse -- every action potential in the motor neuron produces an action potential in the muscle fiber. 0
Kandel; Principles of Neural Science 207 Presynaptic neuron connections require that perhaps 50--100 excitatory neurons fire together to produce a synaptic potential large enough to trigger an action potential. 0
Kandel; Principles of Neural Science 207 John Eccles and his colleagues in the 1950s, synaptic mechanisms of the spinal motor neurons that control the stretch reflex. 0
Kandel; Principles of Neural Science 209 Effect of a presynaptic neuron -- whether it is excitatory or inhibitory -- is determined not by the type of neurotransmitter released from the presynaptic neuron, but by the type of ion channels gated by the neurotransmitter in the postsynaptic cell. 2
Kandel; Principles of Neural Science 209 Vertebrate brain neurons that release glutamate typically act on receptors that produce excitation. 0
Kandel; Principles of Neural Science 209 Neurons that release GABA or glycine act on ionotropic inhibitory receptors. 0
Kandel; Principles of Neural Science 212 Membrane potential of the axon hillock (integrateive component of neurons) to the threshold for generation of an action potential. 3
Kandel; Principles of Neural Science 213 Blockade of the NMDA receptors produces symptoms that resemble the hallucinations associated with schizophrenia. 1
Kandel; Principles of Neural Science 213 Presynaptic neuron fires repeatedly.  This activation of the NMDA receptor leads to the activation of calcium dependent enzymes and certain second messenger-dependent protein kinases in the postsynaptic cell. 0
Kandel; Principles of Neural Science 213 NMDA receptor biochemical reactions are important for triggering signal transduction pathways that contribute to certain long-lasting modifications in the synapse that are important for learning and memory. 0
Kandel; Principles of Neural Science 213 Because NMDA receptors require a significant level of presynaptic activity before they can function maximally, long-term synaptic modifications mediated by the NMDA receptor is often referred to as activity-dependent synaptic modification. 0
Kandel; Principles of Neural Science 213 Excessive amounts of glutamate are highly toxic to neurons. 0
Kandel; Principles of Neural Science 214 Glutamate excitotoxicity. Free radicals that are toxic to the cell.  Glutamate toxicity may contribute to cell damage after stroke. Episodes of rapidly repeated seizures. 1
Kandel; Principles of Neural Science 214 GABA is a major inhibitory transmitter in the brain and spinal cord. 0
Kandel; Principles of Neural Science 214 GABA acts on two receptors, GABAA and GABAB. 0
Kandel; Principles of Neural Science 214 GABAA receptor is an ionotropic receptor that gates a Cl- channel. 0
Kandel; Principles of Neural Science 214 GABAB receptor is a metabotropic receptor that activates a second messenger cascade, which often activates a K+ channel. 0
Kandel; Principles of Neural Science 219 GABA and glycine receptors are structurally related to the nicotinic acetylcholine receptors.  These receptors are thought to be members of one large genetic family. 5
Kandel; Principles of Neural Science 219 Glutamate receptors appear to have evolved from a different class of proteins and represent a second genetic family of ligand gated channels. 0
Kandel; Principles of Neural Science 219 Each subunit of the GABA and glycine receptor channels contains a large extracellular domain at it's amino terminus that contains the ligand binding site. 0
Kandel; Principles of Neural Science 219 Two molecules of GABA and up to three molecules of glysine are required to activate their respective channels. 0
Kandel; Principles of Neural Science 219 Extracellular ligand-binding domain of the subunits is followed by a four hydrophobic transmembrane domains. 0
Kandel; Principles of Neural Science 219 The second transmembrane domain is thought to form the lining of the channel pore. 0
Kandel; Principles of Neural Science 219 GABA-gated channel is the target for three types of drugs that are clinically important and socially abused: the benzodiazepines, barbituates, and alcohol. 0
Kandel; Principles of Neural Science 219 Benzodiazepines -- anti-anxiety agents and muscle relaxants that include Valium. 0
Kandel; Principles of Neural Science 219 Barbiturates comprise a group of hypnotics that includes phenobarbital. 0
Kandel; Principles of Neural Science 219 Four classes of compounds -- GABA, benzodiazepine, barbituates, and alcohol -- act at different sites to increase the opening of the channel and hence enhance inhibitory synaptic transmission. 0
Kandel; Principles of Neural Science 221 Most neurotransmitter-gated channels are normally clustered at postsynaptic sites in the membrane, opposed to presynaptic terminals. 2
Kandel; Principles of Neural Science 222 Each neuron in the central nervous system, whether in the spinal cord or in the brain, is constantly bombarded by synaptic input from other neurons. 1
Kandel; Principles of Neural Science 222 A neuron may be innervated by as many as 10,000 different synaptic endings. 0
Kandel; Principles of Neural Science 222 Some inputs contact a neuron at the extremities of its apical dendrites, others at its proximal dendrites, or on a dendritic shaft, or on dendritic spines.  The different inputs can reinforce or cancel one another. 0
Kandel; Principles of Neural Science 222 Inputs to a neuron do not sum linearly.  Postsynaptic neuron's competing inputs are combined via neuronal integration. 0
Kandel; Principles of Neural Science 222 Decision to initiate an action potential is made at the initial segment of the axon, the axon hillock. 0
Kandel; Principles of Neural Science 222 Axon hillock region of cell membrane has a lower threshold for action potentials than the cell body or dendrites because it has a higher density of voltage-dependent Na+ channels. 0
Kandel; Principles of Neural Science 222 Membrane potential of the axon hillock serves as the readout for the integrative action of a neuron. 0
Kandel; Principles of Neural Science 222 Because neuronal integration involves a summation of synaptic potentials that spread passively to the trigger zone, it is critically affected by two passive membrane properties of the axon -- temporal summation; spatial summation. 0
Kandel; Principles of Neural Science 222 Time constant determines the time course of synaptic potential.  Consecutive synaptic potentials are added together in a postsynaptic cell.  Neurons with a large time constant have a greater capacity for temporal summation. 0
Kandel; Principles of Neural Science 222 Length constant of a cell determines the degree to which a depolarizing current decreases as its spreads passively. 0
Kandel; Principles of Neural Science 223 Voltage-gated channels in dendritic membrane can amplify weak excitatory input that arrives at remote parts of the dendrite. 1
Kandel; Principles of Neural Science 224 Dendrites are complex integrative compartments in nerve cells that can exert powerful orthograde effects on the propagation of synaptic potentials to the cell body as well is powerful retrograde effects on the relay of activity-dependent information from the cell body and axon hillock back to the dendritic synapses. 1
Kandel; Principles of Neural Science 229 Modulation of Synaptic Transmission: Second Messengers 5
Kandel; Principles of Neural Science 229 Metabotropic receptors -- receptor and effector functions of gating are carried out by separate molecules.  This receptor type consists of two families: (1) G protein-coupled kinase receptors and (2) receptor tyrosine kinases. 0
Kandel; Principles of Neural Science 229 In G protein-coupled receptors, the effector is typically an enzyme that produces a diffusible second messenger. 0
Kandel; Principles of Neural Science 229 Second messengers trigger a biochemical cascade, either by activating specific protein kinases that phosphorylate a variety of the cell's proteins or by mobilizing calcium ions from intracellular stores. 0
Kandel; Principles of Neural Science 230 Receptor tyrosine kinases are typically activated by hormones, growth factors, and neuropeptides. 1
Kandel; Principles of Neural Science 230 The number of substances known to act as second messengers in synaptic transmission is far fewer than the number of transmitters. 0
Kandel; Principles of Neural Science 230 Approximately 100 substances function as neurotransmitters, each of which can activate several different receptors on the cell surface. 0
Kandel; Principles of Neural Science 230 (1) gaseous and  (2) nongaseous second messengers. 0
Kandel; Principles of Neural Science 230 The best understood nongaseous second messenger is cyclic adenosine monophosphate (cAMP). 0
Kandel; Principles of Neural Science 230 Intracellular calcium can also serve as a second messenger. 0
Kandel; Principles of Neural Science 230 Gaseous second messengers are highly diffusible. Two best studied are nitric oxide (NO) and carbon monoxide (CO). 0
Kandel; Principles of Neural Science 231 Activated G protein binds to an effector enzyme. 1
Kandel; Principles of Neural Science 231 Phosphorylation mediated by protein kinases is  central to understanding the action of second-messenger pathways. 0
Kandel; Principles of Neural Science 231 A single protein kinase can phosphorylate many different target proteins. 0
Kandel; Principles of Neural Science 231 cAMP pathway is the prototype of an intracellular signaling pathway that makes use of a water-soluble second-messenger that diffuses within the cytoplasm. 0
Kandel; Principles of Neural Science 232 Integral membrane protein that spans the plasma membrane 12 times. 1
Kandel; Principles of Neural Science 234 G proteins are not integral component of the membrane. 2
Kandel; Principles of Neural Science 234 G proteins consist of three subunits: a, b, and g. 0
Kandel; Principles of Neural Science 234 A single ligand receptor can activate many G proteins, thus amplifying a small synaptic signal into many activated cyclase complexes, thereby producing an effective concentration of cAMP within the cell. 0
Kandel; Principles of Neural Science 236 Calcium often acts when it forms a complex with the small protein calmodulin. 2
Kandel; Principles of Neural Science 236 cAMP-dependent protein kinase, or PKA, can become active in the absence of a second messenger, due to the action of proteases that degrade the regulatory regions of the enzymes. Constitutively active kinases are thought to be important for triggering long-term changes in synaptic plasticity associated with certain forms of learning and memory. 0
Kandel; Principles of Neural Science 238 Receptor tyrosine kinases  bind various peptides including nerve growth factor (NGF), and insulin. 2
Kandel; Principles of Neural Science 238 Substrates for tyrosine kinase often produce long-term changes in neuronal function. 0
Kandel; Principles of Neural Science 240 All of these second messenger enzymes are believed to be related to an ancestral enzyme. 2
Kandel; Principles of Neural Science 240 Purkinje cells of the cerebellum have long term depression of synaptic transmission (LTD), a form of synaptic plasticity that may underlie certain forms of motor learning. 0
Kandel; Principles of Neural Science 240 Direct gating of ion channels through the ionotropic receptors is usually rapid -- on the order of milliseconds -- because it involves a change in the conformation of only a single macromolecule. 0
Kandel; Principles of Neural Science 240 Indirect gating of ion channels through metabotropic receptors is slower in onset (tens of milliseconds to seconds) and longer lasting (seconds to minutes) because it involves a cascade of reactions. 0
Kandel; Principles of Neural Science 240 Ligand gated channels function as simple on-off switches. 0
Kandel; Principles of Neural Science 250 Transmitter gated channels produce the fastest and briefest type of synaptic action, lasting only a few milliseconds, on average. 10
Kandel; Principles of Neural Science 250 Fast synaptic transmission mediates most motor actions and perceptual processing. 0
Kandel; Principles of Neural Science 251 Longer-lasting effects of transmitters are mediated by activation of the G protein-coupled receptors and the receptor tyrosine kinases. 1
Kandel; Principles of Neural Science 251 Prominent second messengers include cyclic AMP. 0
Kandel; Principles of Neural Science 251 Many second messenger actions depend on activation of protein kinases, leading to phosphorylation of a variety of cellular proteins, including ion channels, which changes their functional state. 0
Kandel; Principles of Neural Science 251 Second messenger actions generally last from seconds to minutes. 0
Kandel; Principles of Neural Science 251 Second messenger actions do not mediate rapid behaviors but rather serve to modulate the strength and efficacy of fast synaptic transmission -- by modulating: (1) transmitter release, (2) sensitivity of ionotropic receptors, or (3) electrical excitability of the postsynaptic cell. 0
Kandel; Principles of Neural Science 251 Second messenger actions are implicated in emotional states, mood, arousal, and certain forms of learning and memory. 0
Kandel; Principles of Neural Science 251 Longest lasting changes in synaptic transmission involve changes in gene transcription, changes that can persist for days or weeks. 0
Kandel; Principles of Neural Science 251 The more permanent synaptic changes are thought to involve many of the same types of receptors and second messenger pathways involved in the shorter term modulatory actions. However, they may require repeated stimulation and more prolonged action of the second messengers. 0
Kandel; Principles of Neural Science 251 Synaptically induced activation of gene expression is critical for the storage of long-term memory. 0
Kandel; Principles of Neural Science 253 Transmitter Release 2
Kandel; Principles of Neural Science 255 Transmitter release is triggered by calcium influx. 2
Kandel; Principles of Neural Science 258 Transmitter is released in quantal units. 3
Kandel; Principles of Neural Science 258 Although release of synaptic transmitter appears smoothly graded, it is actually released in discrete packages called quanta. 0
Kandel; Principles of Neural Science 262 Each vesicle stores one quantum of transmitter, amounting to several thousand molecules. 4
Kandel; Principles of Neural Science 264 To catch vesicles in the act of exocytosis, quick freeze the tissue with liquid helium. 2
Kandel; Principles of Neural Science 267 Synaptic vesicles are recycled. 3
Kandel; Principles of Neural Science 267 Vesicle membrane is a rapidly recycled. 0
Kandel; Principles of Neural Science 274 Amount of transmitter release can be modulated by regulating the amount of calcium influx during the action potential. 7
Kandel; Principles of Neural Science 274 Transmitter release depends strongly on the intracellular Ca2+ concentration. 0
Kandel; Principles of Neural Science 274 A slight depolarization of the membrane can increase the steady-state influx of Ca2+ and thus enhance the amount of neurotransmitter released by subsequent action potentials. 0
Kandel; Principles of Neural Science 274 Synaptic effectiveness can be altered in most nerve cells by intense activity. 0
Kandel; Principles of Neural Science 274 High-frequency stimulation of the presynaptic neuron can generate 500-1000 action potential's per second. 0
Kandel; Principles of Neural Science 274 Postsynaptic potentiation usually lasts several minutes, but can persist for an hour or more. 0
Kandel; Principles of Neural Science 275 Presynaptic cell stores information about the history of its activity in the form of residual Ca2+ in its terminals 1
Kandel; Principles of Neural Science 275 Storage of biochemical information in the nerve cell after a brief period of activity, leads to a strengthening of the presynaptic connection that persist for many minutes. 0
Kandel; Principles of Neural Science 275 Long-term potentiation (LTP) can last for many hours or even days. 0
Kandel; Principles of Neural Science 277 Neurotransmitter is packaged in the vesicles, each containing approximately 5000 transmitter molecules. 2
Kandel; Principles of Neural Science 277 Synaptic potentials evoked by nerve stimulation are composed of integral multiples of quantal potential. 0
Kandel; Principles of Neural Science 277 Increasing the extracellular calcium does not change the size of the quantal synaptic potential.  Rather, it increases the probability that a vesicle discharges its transmitter.  As a result, there is an increase in the number of vesicles released. 0
Kandel; Principles of Neural Science 277 High-frequency stimulation produces an increase in transmitter release call posttetanic potentiation. 0
Kandel; Principles of Neural Science 277 Posttetanic potentiation lasts a few minutes and is caused by Ca2+ left in the terminal after the large Ca2+ influx that occurs during a train of action potentials. 0
Kandel; Principles of Neural Science 280 Neurotransmitters 3
Kandel; Principles of Neural Science 280 Bernard Katz in the 1950s -- transmitters are stored in vesicles at synapses and released by exocytosis. 0
Kandel; Principles of Neural Science 281 Nervous system make use of two main classes of chemical substances for signaling -- small molecule transmitters and neuroactive peptides. 1
Kandel; Principles of Neural Science 281 Small molecule transmitters are packaged in small vesicles, which release their contents through exocytosis at active zones closely associated with specific Ca2+ channels. 0
Kandel; Principles of Neural Science 281 Small synaptic vesicles are characteristic of neurons that use acetylcholine, glutamate, GABA, and glysine as transmitters. 0
Kandel; Principles of Neural Science 281 Large dense core vesicles are typical of catecholaminergic and serotonergic neurons. 0
Kandel; Principles of Neural Science 282 Catecholamine transmitters -- dopamine, norepinephrine, and epinephrine -- are all synthesized from the essential amino acid tyrosine. 1
Kandel; Principles of Neural Science 283 Synthesis of biogenic amines is highly regulated. As a result, the amounts of transmitter available for release can keep up with wide variations in neuronal activity. 1
Kandel; Principles of Neural Science 283 Serotonergic neurons are found in and around the midline raphe nuclei of the brainstem, which are involved in regulating attention and other complex cognitive functions. 0
Kandel; Principles of Neural Science 283 Serotonin is implicated in depression, a major disorder of mood. 0
Kandel; Principles of Neural Science 284 Glutamate is a neurotransmitter most frequently used throughout the central nervous system. 1
Kandel; Principles of Neural Science 285 Glutamate and other neurotransmitters are taken up from the synaptic cleft by both neurons and glia. 1
Kandel; Principles of Neural Science 285 Glutamate is excitatory at ionotropic receptors and modulatory at metabotropic receptors. 0
Kandel; Principles of Neural Science 285 In the brain, GABA is the major transmitter in various inhibitory interneurons. 0
Kandel; Principles of Neural Science 285 GABA is inhibitory at the neuromuscular junction of the lobster (and of other crustacea and insects), and glutamate is excitatory. 0
Kandel; Principles of Neural Science 285 Transmitter glutamate is compartmentalized in synaptic vesicles. 0
Kandel; Principles of Neural Science 286 Many neuroactive peptides serve as transmitters. 1
Kandel; Principles of Neural Science 286 Small molecule transmitter substances can be formed in all parts of the neuron. They can be synthesized at the nerve terminals where they are released. 0
Kandel; Principles of Neural Science 286 In contrast, neuroactive peptides are derived from secretory proteins that are formed in the cell body. 0
Kandel; Principles of Neural Science 286 Like other secretory proteins, neuroactive peptides or their precursors are first processed in the endoplasmic reticulum, and then move to the Golgi apparatus to be processed further. 0
Kandel; Principles of Neural Science 286 Neuroactive peptides leave the Golgi apparatus within secretory granules and move to terminals by fast axonal transport. 0
Kandel; Principles of Neural Science 286 More than 50 short peptides are pharmacologically active in nerve cells. 0
Kandel; Principles of Neural Science 286 Hormones in some tissues also act as transmitters when released close to the site of intended action. 0
Kandel; Principles of Neural Science 286 The diversity of neuroactive peptides is enormous. 0
Kandel; Principles of Neural Science 289 Relatedness between the seven main families of peptides is made by comparing either the amino acid sequences of the peptides or the nucleotide base sequences in the genes that encode them. 3
Kandel; Principles of Neural Science 294 Timely removal of transmitters from the synaptic cleft is critical to synaptic transmission. 5
Kandel; Principles of Neural Science 294 Transmitters are removed from the cleft by three mechanisms -- diffusion, enzymatic degradation, and reuptake. 0
Kandel; Principles of Neural Science 294 Diffusion removes some fraction of all chemical messengers. 0
Kandel; Principles of Neural Science 294 Enzymatic degradation of transmitter is used primarily by cholinergic synapses. 0
Kandel; Principles of Neural Science 294 Neuroactive peptides are removed more slowly than small molecule transmitters from the synaptic cleft. 0
Kandel; Principles of Neural Science 294 The slow removal of neuropeptides contributes to the long duration of their effects. 0
Kandel; Principles of Neural Science 294 Reuptake of transmitter substance is the most common mechanism for inactivation. 0
Kandel; Principles of Neural Science 294 High affinity uptake, with binding constants of 25 µM or less for the released transmitter, is mediated by transport of molecules in the membranes of nerve terminals and glial cells. 0
Kandel; Principles of Neural Science 295 Cocaine blocks the reuptake of norepinephrine. 1
Kandel; Principles of Neural Science 295 Tricyclic antidepressants and selective serotonin reuptake inhibitors such as Prozac block the reuptake of serotonin. 0
Kandel; Principles of Neural Science 295 The 12 membrane spanning group of transporter molecules includes several transporters for each transmitter; for example, there are at least four for GABA. 0
Kandel; Principles of Neural Science 295 All members of the membrane transporter molecules are related, stemming from ancestor protein that gives rise to bacterial permeases. 0
Kandel; Principles of Neural Science 295 Concentration of transmitter is much higher in the terminal than in the synaptic cleft, typically by four orders of magnitude. 0
Kandel; Principles of Neural Science 295 The electrochemical potential of the membrane transporter molecules is sufficient to take up the dilute transmitter into the cell. 0
Kandel; Principles of Neural Science 295 Several membrane soluble molecules diffuse through the neuronal membrane and are released without being packaged in vesicles. 0
Kandel; Principles of Neural Science 295 The most prominent of the membrane-diffusing molecules is the gas nitric oxide (NO). 0
Kandel; Principles of Neural Science 295 The membrane soluble molecules may act as retrograde messengers at some synapses, carring information from the postsynaptic neurons in the presynaptic cell. 0
Kandel; Principles of Neural Science 295 None of the chemical messages carries unique information, as RNA and DNA do. 0
Kandel; Principles of Neural Science 295 Transmittal molecules become signals when they bind to receptor proteins in the membrane of another cell, causing the receptor proteins to change shape. 0
Kandel; Principles of Neural Science 296 Two major classes of chemical messengers -- small molecule transmitters and neuroactive peptides. 1
Kandel; Principles of Neural Science 296 Nerve endings contain a high concentration of synaptic vesicles. 0
Kandel; Principles of Neural Science 296 Small molecule transmitter in a neuron must be synthesized at the terminal. 0
Kandel; Principles of Neural Science 296 Protein precursors of neuroactive peptides are synthesized only in the cell body, then become packaged in secretory granules and synaptic vesicles that are transported from the cell body to the terminals. 0
Kandel; Principles of Neural Science 298 Myasthenia Gravis 2
Kandel; Principles of Neural Science 313 Neural science, the modern science of the brain, emerged in the mid-1970s. 15
Kandel; Principles of Neural Science 313 Cognitive neuroscience is a pragmatic attempt to merge neural science with psychology. 0
Kandel; Principles of Neural Science 317 Anatomical organization of the Central Nervous System. 4
Kandel; Principles of Neural Science 319 Behavior is shaped in response to stimuli in our environment. 2
Kandel; Principles of Neural Science 319 Topographically organized neural map of the receptive circuits in the brain. 0
Kandel; Principles of Neural Science 319 Parallel processing of sensory information. 0
Kandel; Principles of Neural Science 319 Perceptions generated by the sensory systems recruit the amygdala, which colors perception with emotion, and the hippocampus, which stores aspects of perception in long-term memory. 0
Kandel; Principles of Neural Science 319 Central nervous system consists of the spinal cord and brain. 0
Kandel; Principles of Neural Science 319 Six major brain divisions: medulla, pons, cerebellum, midbrain, diencephalon, and cerebral hemispheres or telencephalon. Each of these divisions is found in both hemispheres. 0
Kandel; Principles of Neural Science 319 Spinal cord is divided into gray matter and surrounding white matter. 0
Kandel; Principles of Neural Science 319 Gray matter of the spinal cord, which contains nerve cell bodies, is typically divided into dorsal and ventral horns. 0
Kandel; Principles of Neural Science 319 Dorsal horn contains an orderly arrangement of sensory relay neurons that receive input from the periphery, while the ventral horn contains motor neurons that innervate specific muscles. 0
Kandel; Principles of Neural Science 319 Spinal cord white matter is made up of longitudinal tracts of myelinated axons that form ascending pathways through which sensory information reaches the brain and desending pathways that carry motor commands and modulatory influences from the brain. 0
Kandel; Principles of Neural Science 319 Nerve fibers that link the spinal cord with the muscles and sensory receptors in the skin are bundled in 31 pairs of spinal nerves, each of which has a sensory division that emerges from the dorsal root and a motor division that emerges from the ventral root. 0
Kandel; Principles of Neural Science 320 Different classes of axons in the dorsal roots mediate sensations of pain, temperature, and touch. 1
Kandel; Principles of Neural Science 322 Pons lies rostral to the medulla and protrudes from the ventral surface of the brain stem. 2
Kandel; Principles of Neural Science 322 Substantia nigra, a distinct nucleus of the midbrain, provides dopaminergic input to a portion of the basal ganglia that regulates voluntary movements. 0
Kandel; Principles of Neural Science 322 Cerebellum, which lies over the pons, contains a far greater number of neurons than any other single subdivision of the brain. 0
Kandel; Principles of Neural Science 322 Cerebellum contains relatively few neuronal types, and its circuitry is well understood. 0
Kandel; Principles of Neural Science 322 Cerebellum is important for maintaining posture and for coordinating head and eye movements, and is also involved in fine tuning the movements of muscles and in learning motor skills. 0
Kandel; Principles of Neural Science 322 Cerebellum is also involved in language and other cognitive functions. 0
Kandel; Principles of Neural Science 324 In most brain systems information processing is organized hierarchically. 2
Kandel; Principles of Neural Science 325 Insular cortex -- some structures of the cerebral hemispheres cannot be seen from the surface of the brain. (diagram) 1
Kandel; Principles of Neural Science 325 Cerebral cortex is divided into four major lobes: frontal, parietal, temporal, occipital. 0
Kandel; Principles of Neural Science 325 Temporal lobe has distinct regions that carry out auditory, visual, and memory functions. 0
Kandel; Principles of Neural Science 325 Cingulate cortex surrounds the dorsal surface of the corpus callosum. 0
Kandel; Principles of Neural Science 325 Overhanging portion of the cerebral cortex that buries the insular within the lateral sulcus is called the operculum. 0
Kandel; Principles of Neural Science 325 Lateral sulcus or Sylvian fissure separates the temporal lobe from the frontal and parietal lobes. 0
Kandel; Principles of Neural Science 325 Insular cortex forms the medial limit of a lateral sulcus. 0
Kandel; Principles of Neural Science 325 Central sulcus runs medially and laterally on the dorsal surface of the hemisphere and separates the frontal and parietal lobes. 0
Kandel; Principles of Neural Science 325 "Limbic lobe" -- portions of the frontal, parietal, and temporal lobes encircle and border the fluid filled ventricles of the brain. 0
Kandel; Principles of Neural Science 325 Cingulate cortex, which surrounds the corpus callosum, is considered a separate division of the neocortex, much like the insular cortex. 0
Kandel; Principles of Neural Science 326 Primary motor cortex mediates voluntary movements of the limbs and trunk.  It is called primary because it contains neurons that project directly to the spinal cord. 1
Kandel; Principles of Neural Science 326 Primary sensory areas receive most of their information directly from the thalamus; only a few synaptic relays are interposed between the thalamus and the peripheral receptors. 0
Kandel; Principles of Neural Science 326 Primary somatosensory cortex is located caudal to the central sulcus, on the post-central gyrus, in the parietal lobe. 0
Kandel; Principles of Neural Science 326 Primary motor cortex, located just rostral to the central sulcus. 0
Kandel; Principles of Neural Science 326 Primary motor cortex is the final site in the cortex for processing motor commands. 0
Kandel; Principles of Neural Science 327 The most typical form of neocortex contains six layers. 1
Kandel; Principles of Neural Science 327 Layer 1 -- an acellular layer.  Occupied by dendrites of cells located deeper in the cortex, and axons that travel through to form connections. 0
Kandel; Principles of Neural Science 327 Layer 2 -- comprised mainly of small spherical cells called granule cells, and is called the external granule cell layer. 0
Kandel; Principles of Neural Science 327 Layer 3 -- contains a variety of cell types, many of which are pyramidally shaped.  Layer 3 is called the external pyramidal cell  layer. 0
Kandel; Principles of Neural Science 327 Layer 4 -- like layer 2, is made up primarily of granule cells and is called the internal granule cell layer. 0
Kandel; Principles of Neural Science 327 Layer 5 -- internal pyramidal cell layer, contains mainly pyramidal cells that are typically larger than those in layer 3. 0
Kandel; Principles of Neural Science 327 layer 6 -- a fairly heterogeneous layer of neurons.  Blends into the white matter. 0
Kandel; Principles of Neural Science 327 Layers 1-3 contain apical dendrites of neurons that have their cell bodies in layers 5 and 6. 0
Kandel; Principles of Neural Science 327 Layers 5 and 6 contain the basal dendrites of neurons with cell bodies and layers 3 and 4. 0
Kandel; Principles of Neural Science 327 Profile of inputs to a particular cortical neuron depends more on the distribution of his dendrites than on the location of the cell body. 0
Kandel; Principles of Neural Science 327 Layer 4 is the main target of sensory information arriving from the thalamus. 0
Kandel; Principles of Neural Science 327 In a highly visual animals, such as humans, the lateral geniculate nucleus provides a large and highly organized input to layer 4 of the primary visual cortex. 0
Kandel; Principles of Neural Science 327 Association or feed-forward connections originate mainly from cells in layer 3 and terminate mainly in layer 4. 0
Kandel; Principles of Neural Science 328 Brodmann's areas (diagram) 1
Kandel; Principles of Neural Science 329 Feedback projections from later to earliest stages of processing, originate from cells in layers 5 and 6 and terminate in layers 1, 2 and 6. 1
Kandel; Principles of Neural Science 329 Local interneurons use the inhibitory neurotransmitter GABA, constitute 20-25% of the neurons in the neocortex, and are located in all layers. 0
Kandel; Principles of Neural Science 329 Basket cells. 0
Kandel; Principles of Neural Science 329 Chandelier cells. 0
Kandel; Principles of Neural Science 329 Excitatory interneurons, located primarily in layer 4, are the primary recipients of sensory information received in the neocortex from the thalamus. 0
Kandel; Principles of Neural Science 329 Neurons in the neocortex have a columnar organization.  A cortical column would fit within a cylinder a fraction of a millimeter in diameter. 0
Kandel; Principles of Neural Science 331 Neurons within a particular column tend to have very similar response properties, presumably because they form a local processing network. 2
Kandel; Principles of Neural Science 331 Columns are thought to be the fundamental computational modules of the neocortex. 0
Kandel; Principles of Neural Science 331 Thickness of the neocortex is always between 2 and 4 mm. 0
Kandel; Principles of Neural Science 331 What differentiates the cerebral cortex of a human from that of a rat is not the thickness of the cortex or the organization of the cortical columns, but the total number of columns. 0
Kandel; Principles of Neural Science 331 Massive expansion of the surface area of the cerebral cortex in humans accommodates many more columns and thus provide greater computational power. 0
Kandel; Principles of Neural Science 331 Ability of the cerebral cortex to process sensory information, to associate it with emotional states, to store it as memory, and to initiate action, is modulated by three structures that lie deep within the cerebral hemispheres: (1) basal ganglia, (2) hippocampal formation, (3) amygdala. 0
Kandel; Principles of Neural Science 331 Major components of the basal ganglia are: (1) caudate nucleus, (2) putamen, (3) globus pallidus. 0
Kandel; Principles of Neural Science 331 Neurons in the basal ganglia regulate movement and contribute to certain forms of cognition such as the learning of skills. 0
Kandel; Principles of Neural Science 331 Basal ganglia receive inputs from all parts of the cerebral cortex but send their output only to the frontal lobe through the thalamus. 0
Kandel; Principles of Neural Science 331 Hippocampus and associated cortical regions form the floor of the temporal horn of the lateral ventricle. 0
Kandel; Principles of Neural Science 331 Damage to the hippocampus causes people to become unable to form new memories, but does not significantly impair old memories. 0
Kandel; Principles of Neural Science 331 Amygdala, which lies just rostral to the hippocampus, is involved in analyzing the emotional or motivational significance of sensory stimuli. 0
Kandel; Principles of Neural Science 331 Amygdala receives input directly from the major sensory systems. 0
Kandel; Principles of Neural Science 331 Through its projections to the brainstem, the amygdala can modulate somatic and visceral components of the peripheral nervous system and thus orchestrate the body's response to a particular situation. 0
Kandel; Principles of Neural Science 331 Responses to danger -- the sense of fear and change in heart rate and respiration that result from seeing a snake -- are mediated by the amygdala and its connections. 0
Kandel; Principles of Neural Science 331 Neuronal cell bodies are grouped in clusters of different sizes and shapes called nuclei. 0
Kandel; Principles of Neural Science 331 Most nuclei are not homogeneous populations of cells, but instead include a variety of cells organized into subnuclei, divisions, or layers. 0
Kandel; Principles of Neural Science 332 Insular cortex, shown in several coronal sections (diagram)  7
Kandel; Principles of Neural Science 332 Reticular formation, a region of the brain stem so named because of its diffuse and relatively nonnuclear appearance. 1
Kandel; Principles of Neural Science 333 In situ hybridization allows neurons to be visualized based on the genes they express. 1
Kandel; Principles of Neural Science 333 Types of neurons within a particular brain nucleus and the connections that they make are the end result of a stereotypical developmental program of cellular proliferation, migration, and differentiation. 0
Kandel; Principles of Neural Science 334 Small groups of noradrenaline and serotonin modulatory neurons in the brain stem set the general arousal level of an animal through their influences on forebrain structures. 1
Kandel; Principles of Neural Science 334 Physiological satisfaction an animal experiences in consuming food reinforces behaviors that led to successful predation.  Modulatory systems of the dopaminergic neurons in the midbrain mediate these rewarding aspects of behavior. 0
Kandel; Principles of Neural Science 334 How the brain's modulatory systems concerned with the reward, attention, and motivation interacts with the sensory and motor systems remains one of the most interesting questions in neuroscience. 0
Kandel; Principles of Neural Science 335 Parasympathetic system acts to conserve body resources and restore homeostasis. 1
Kandel; Principles of Neural Science 335 Human nervous system is comprised of several hundreds of billions of neurons, each of which receives and gives rise to tens of thousands of connections. 0
Kandel; Principles of Neural Science 335 Some nerve connections are located nearly a meter from the cell bodies of origin. 0
Kandel; Principles of Neural Science 335 Central nervous system consists of the brain and spinal cord, and peripheral nervous system composed of specialized classes of neurons (ganglia) and peripheral nerves. 0
Kandel; Principles of Neural Science 335 Electron microscope methods of neural anatomy in the 1950s revealed the structure of synapses. 0
Kandel; Principles of Neural Science 335 Some synaptic terminals are located on dendrites, others on axon terminals, and still others on soma of the postsynaptic cell. 0
Kandel; Principles of Neural Science 335 Location of synapses on the neuronal surface critically affects the function of the cell. 0
Kandel; Principles of Neural Science 337 Functional organization of Perception and Movement 2
Kandel; Principles of Neural Science 338 Major anatomical features of the spinal cord.  Ventral horn and carries large motor neurons.  Dorsal horn carries somatosensory information from the lower limbs. (diagram) 1
Kandel; Principles of Neural Science 341 Submodalities of somatic sensation -- touch, pain, and positions sense -- are processed in the brain through different pathways that end in different brain regions. 3
Kandel; Principles of Neural Science 341 Thalamus is an oval shaped structure that constitutes the dorsal portion of the diencephalon. 0
Kandel; Principles of Neural Science 341 As many as 50 thalamic nuclei have been identified. 0
Kandel; Principles of Neural Science 341 Primary somatosensory cortex in the postcentral gyrus. 0
Kandel; Principles of Neural Science 341 Axons of cells in the ventual posterior lateral nucleus of the thalamus project to the primary somatosensory cortex in the post-central gyrus. 0
Kandel; Principles of Neural Science 341 Some axons in the thalamus participate in motor functions, transmitting information from the cerebellum and basal ganglia to the motor regions of the frontal lobe. 0
Kandel; Principles of Neural Science 341 Axons from cells in the thalamus that project to the neocortex travel in the internal capsule, a large fiber bundle that carries most of the axons running to and from the cerebral hemisphere. 0
Kandel; Principles of Neural Science 341 Through its connections with the frontal lobe, the thalamus may play a role in cognitive functions such as memory. 0
Kandel; Principles of Neural Science 341 Some thalamic nuclei that may play a role in attention project diffusely to large but distinctly different regions of cortex. 0
Kandel; Principles of Neural Science 341 Reticular nucleus, which forms the outer shell of the thalamus, does not project to the neocortex at all. 0
Kandel; Principles of Neural Science 341 Reticular nucleus receives inputs from other fibers as they exit the thalamus en route to the neocortex and in turn projects to the other thalamic nuclei, thus providing feedback to the output nuclei of the thalamus. 0
Kandel; Principles of Neural Science 341 Groups of neurons are located within the fibers of the internal medullary lamina and are collectively referred to as the intralamina nuclei. 0
Kandel; Principles of Neural Science 341 Ventral anterior and ventral lateral nuclei of the thalamus are important for motor control and carry information from the basal ganglia and cerebellum to the motor cortex. 0
Kandel; Principles of Neural Science 341 Medial geniculate nucleus is a component of the auditory system and conveys tonotopically organized auditory information to the superior temporal gyrus of the temporal lobe. 0
Kandel; Principles of Neural Science 343 Pulvinar is extensively interconnected with widespread regions of the parietal, temporal, and occipital lobes, as well as with the superior colliculus and other nuclei of the brainstem related to vision. 2
Kandel; Principles of Neural Science 343 Thalamus not only projects to the visual areas of the neocortex but also receives a return projection from the neocortex.  The return projection from the occipital cortex accounts for a greater number of synapses in the lateral geniculate nucleus than does the retinal input! 0
Kandel; Principles of Neural Science 343 Most nuclei of the thalamus receive a prominent return projection from the cerebral cortex. 0
Kandel; Principles of Neural Science 343 Intralamina nuclei of the thalamus project to limbic structures such as the amygdala and hippocampus, but also send projections to components of the basal ganglia. 0
Kandel; Principles of Neural Science 343 Reticular nucleus -- outer covering of the thalamus formed by a sheet-like structure. 0
Kandel; Principles of Neural Science 344 Most of the neurons of the reticular nucleus use the inhibitory transmitter GABA, whereas most other thalamic neurons utilize the excitatory transmitter glutamate. 1
Kandel; Principles of Neural Science 344 Reticular nucleus modulates activity of other thalamic nuclei based on its monitoring of the entirety of the thalamocortical stream of information. 0
Kandel; Principles of Neural Science 344 Thalamus is not a relay station where information is simply passed on to the neocortex. Rather, it is a complex brain region where substantial information processing is possible. 0
Kandel; Principles of Neural Science 344 An example; output of somatosensory information from the ventral posterior lateral nucleus is subject to four types of processing: (1) local processing within the nucleus; (2) modulation by brain stem inputs, such as the noradrenergic and serotonergic monoamine systems; (3) inhibitory feedback from the reticular nucleus; and (4) excitatory feedback from the neocortex. 0
Kandel; Principles of Neural Science 344 All portions of the body are represented in the cortex somatotopically, but not in proportion to body mass. 0
Kandel; Principles of Neural Science 345 Somatosensory cortex contains not one but several topographically organized sets of inputs from the skin and therefore several somatotopic maps of the body surface. 1
Kandel; Principles of Neural Science 345 Primary somatosensory cortex has four complete maps of the skin, one each in areas 3a, 3b, 1, and 2. 0
Kandel; Principles of Neural Science 345 At higher levels of the hierarchy, somatosensory information is used in motor control, eye-hand coordination, and memory related to tactical experience and touch. 0
Kandel; Principles of Neural Science 345 Close linkage between the somatosensory and motor functions of the cortex. 0
Kandel; Principles of Neural Science 347 Voluntary Movement Diagram (diagram) 2
Kandel; Principles of Neural Science 347 A major function of the perceptual systems is to provide sensory information necessary for the actions mediated by the motor systems of the brain and spinal cord. 0
Kandel; Principles of Neural Science 347 Primary motor cortex is organized somatotopically like the somatic sensory cortex. 0
Kandel; Principles of Neural Science 347 Human corticospinal track consists of about one million axons, of which about 40% originate in the motor cortex. 0
Kandel; Principles of Neural Science 347 Pyramidal tract -- medullary pyramids, prominent protuberances on the ventral surface of the medulla. 0
Kandel; Principles of Neural Science 347 Corticospinal tract makes monosynaptic connections with motor neurons, connections that are particularly important for individual finger movements. 0
Kandel; Principles of Neural Science 348 Indirect connections are important for coordinating larger groups of muscles and behaviors such as reaching and walking. 1
Kandel; Principles of Neural Science 348 Major influence of the cerebellum on movement is through its connections to the ventral nuclear group of the thalamus, which connects directly to the motor cortex. 0
Kandel; Principles of Neural Science 348 Fibers of the basal ganglia and cerebellum terminate in distinctly different portions of the ventral nuclear complex and influence different portions of both the somatosensory and motor regions of the cortex. 0
Kandel; Principles of Neural Science 348 Sensations of touch and pain are mediated by different pathways. 0
Kandel; Principles of Neural Science 348 All sensory and motor systems follow the pattern of hierarchical and parallel processing. 0
Kandel; Principles of Neural Science 348 Brain constructs an internal representation of external physical events after first analyzing various features of those events. 0
Kandel; Principles of Neural Science 349 Integration of Sensory and Motor function: Association areas of the cerebral cortex; Cognitive capabilities of the brain 1
Kandel; Principles of Neural Science 349 All mental functions are localizable to specific areas of the brain. 0
Kandel; Principles of Neural Science 349 Complex mental functions require integration of information from several cortical areas. 0
Kandel; Principles of Neural Science 349 Cortex is organized hierarchically.  Some cortical areas serve higher order integrative functions that are neither purely sensory nor purely motor, but associative. 0
Kandel; Principles of Neural Science 349 Association areas perform mental processes that intervene between sensory inputs and motor outputs. 0
Kandel; Principles of Neural Science 349 Association area mental processes include: interpretation of sensory information, association of perceptions with previous experience, focusing of attention, and exploration of the environment. 0
Kandel; Principles of Neural Science 350 Each primary sensory cortex projects to nearby higher-order areas of sensory cortex that integrate afferent information for a single sensory modality. 1
Kandel; Principles of Neural Science 350 Unimodal association areas project to multimodal sensory association areas that integrate information about more than one sensory modality. 0
Kandel; Principles of Neural Science 350 Multimodal sensory association areas project to multimodal motor association areas located rostral to the primary motor cortex in the frontal lobe. 0
Kandel; Principles of Neural Science 350 Primary motor areas are the final sites for the cortical processing of motor commands. 0
Kandel; Principles of Neural Science 350 Multimodal association areas are the anatomical substrates of the highest brain functions -- conscious thought, perception, and goal-directed action. 0
Kandel; Principles of Neural Science 353 Frontal lobes play a critical role in long-term planning and judgment. 3
Kandel; Principles of Neural Science 353 Hierarchical model of information processing in the cerebral cortex -- sensory information is first received and interpreted by the primary sensory areas, then sent to the unimodal association areas, and finally to the multimodal sensory areas. 0
Kandel; Principles of Neural Science 353 Object and pattern recognition in the inferotemporal cortex. 0
Kandel; Principles of Neural Science 353 Posterior association areas that process sensory information are highly interconnected with the frontal association areas responsible for planning and motor actions. 0
Kandel; Principles of Neural Science 354 Visual, auditory, or somatic information converge in multimodal association areas in the prefrontal, parietotemporal, and limbic cortices. 1
Kandel; Principles of Neural Science 354 Multimodal sensory association cortex in the inferior parietal lobule is concerned with directing visual attention to objects in the contralateral visual field. 0
Kandel; Principles of Neural Science 354 Position of a stimulus in the world as well as its relationship to the individual's personal space. 0
Kandel; Principles of Neural Science 354 Personal space may be within arm's reach. 0
Kandel; Principles of Neural Science 354 Extrapersonal space if it is across the room. 0
Kandel; Principles of Neural Science 355 Cingulate cortex -- limbic association area. 1
Kandel; Principles of Neural Science 355 Superior temporal lobe (Wernicke's area) -- meaning of spoken words is analyzed, extracting language information from the ongoing sensory strain. 0
Kandel; Principles of Neural Science 355 Posterior association areas are heavily interconnected with the association cortex of the frontal lobe. 0
Kandel; Principles of Neural Science 355 Motor planning begins with a general outline of behavior and is translated into concrete motor responses through processing in the motor pathways. 0
Kandel; Principles of Neural Science 355 Primary motor cortex occupies the precentral gyrus. 0
Kandel; Principles of Neural Science 355 Premotor cortex is a set of interconnected areas in the frontal lobe just rostral to the motor cortex.  Premotor cortex includes areas 6 and 8 and the supplementary motor cortex on the medial surface of the hemisphere. 0
Kandel; Principles of Neural Science 355 Lesions of the primary motor cortex produce complete absence of voluntary movement, although some postural and stereotyped involuntary movements may persist. 0
Kandel; Principles of Neural Science 355 Premotor cortex receives inputs mainly from three sources: (1) motor nuclei in the ventroanterior and ventrolateral thalamus (which receive input from the basal ganglia and the cerebellum); (2) primary somatosensory cortex and parietal association cortex (which provide information about the ongoing motor response); (3) prefrontal association cortex. 0
Kandel; Principles of Neural Science 356 Prefrontal cortex has three main regions: (1) lateral prefrontal cortex, (2) medial prefrontal cortex, and (3) orbitofrontal cortex. 1
Kandel; Principles of Neural Science 356 Orbitofrontal cortex and medial prefrontal cortex are related to the limbic association cortex and connect directly to limbic structures such as the amygdala and cingulate cortex. 0
Kandel; Principles of Neural Science 356 To select appropriate motor responses, frontal association areas must integrate sensory information from both the outside world and the body. 0
Kandel; Principles of Neural Science 356 Prefrontal association area is specifically concerned with the sequencing of behaviors over time. 0
Kandel; Principles of Neural Science 356 Prefrontal association area is engaged in tasks that require a delay between a stimulus and a behavioral response or that depend heavily upon recent experience. 0
Kandel; Principles of Neural Science 357 The idea of working memory was introduced in 1974 by the cognitive psychologist Alan Baddeley. 1
Kandel; Principles of Neural Science 357 Working memory has three distinct components: one for verbal memories; a parallel component for visual memories; and a third component that functions as a central executive. 0
Kandel; Principles of Neural Science 359 Brain's analysis of a visual scene is carried out in two major parallel pathways; (1) a ventral pathway through the inferior temporal lobe that processes information about color and shape of objects (what the visual image is about) and (2) a dorsal pathway through the posterior parietal cortex that processes information about the location of objects (where the visual image is located). 2
Kandel; Principles of Neural Science 361 Prefrontal area of humans and other animals has a particularly prominent dopaminergic innervation. 2
Kandel; Principles of Neural Science 362 Disturbances of the dopaminergic system are thought to contribute to the symptoms of schizophrenia. 1
Kandel; Principles of Neural Science 362 Cognitive deficits and schizophrenia may involve difficulty in appropriately activating prefrontal areas. 0
Kandel; Principles of Neural Science 362 Dorsolateral prefrontal association cortex and parietal association cortex are among the most densely interconnected regions of association cortex, and both project to numerous common cortical and subcortical structures. 0
Kandel; Principles of Neural Science 363 Patients with damage to Wernicke's area will be unaware of the symbolic content of language. 1
Kandel; Principles of Neural Science 363 Split-brain patients -- surgically sectioned corpus callosum and anterior commissure to control chronic epileptic seizures. 0
Kandel; Principles of Neural Science 363 Split-brain patients seem to have two independent conscious selves. 0
Kandel; Principles of Neural Science 363 A broad range of cognitive functions are mediated by the right hemisphere alone. 0
Kandel; Principles of Neural Science 365 Even the most complex functions of the brain are localized to specific combinations of regions. 2
Kandel; Principles of Neural Science 365 Whether function is a localized or an ensemble property of the nervous system appears to be a dialectical issue. 0
Kandel; Principles of Neural Science 365 No part of the nervous system functions in the same way alone as it does in concert with other parts. 0
Kandel; Principles of Neural Science 366 Primary sensory input and final motor output are conveyed in pathways that are topographically organized so as to constitute topographic maps of both the receptor surface and the muscles for movement. 1
Kandel; Principles of Neural Science 366 Resolution of routine MRI is about 1 mm. 0
Kandel; Principles of Neural Science 366 MRI field strengths of 4 Tesla provide images with resolution of less than 1 mm. 0
Kandel; Principles of Neural Science 367  MRI scan midsagittal section with interpretive illustration (diagram) 1
Kandel; Principles of Neural Science 368 MRI scan horizontal section with interpretive illustration (diagram) 1
Kandel; Principles of Neural Science 369 MRI scan coronal section with interpretive illustration (diagram) 1
Kandel; Principles of Neural Science 370 Magnetic resonance imaging 1
Kandel; Principles of Neural Science 374 Functional MRI (fMRI) makes use of blood oxygen level detection (BOLD), an index of brain activity composed of several variables. 4
Kandel; Principles of Neural Science 374 BOLD is a sensitive method for measuring cerebral cortical activity that has considerably greater spatial resolution than PET scanning. 0
Kandel; Principles of Neural Science 375 Positron emission tomography (PET) is a sensitive method of imaging based on the detection of a trace amounts of radioactive isotopes. 1
Kandel; Principles of Neural Science 375 PET method is limited to a few research centers because the short-lived radioisotopes must be generated locally in a cyclotron. 0
Kandel; Principles of Neural Science 376 Positron emission tomography 1
Kandel; Principles of Neural Science 379 Because MRI images are sharp, PET and other functional techniques often done concomitantly with MRI to take advantage of MRI's ability to locate within the brain the site of the isotope signal detected by a PET scanning. 3
Kandel; Principles of Neural Science 379 Functional imaging techniques can be used for studies of normal subjects involving cognitive processes such as attention, perception, memory, or language. 0
Kandel; Principles of Neural Science 381 Nerve cells to cognition: Internal cellular representation required for Perception and Action 2
Kandel; Principles of Neural Science 382 Behaviorism's most influential period, the 1950s. 1
Kandel; Principles of Neural Science 383 Early cognitive psychologists, building on the evidence from the Gestalt psychology, psychoanalysis, and European neurology. 1
Kandel; Principles of Neural Science 383 Cognitive approach to behavior assumes that each perceptual or motor act has an internal representation in the brain. 0
Kandel; Principles of Neural Science 383 An internal representation for a perceptual or motor act must have the form of a distinctive pattern of neural activity. 0
Kandel; Principles of Neural Science 383 Mechanisms of perception are much the same in humans and monkeys. 0
Kandel; Principles of Neural Science 384 Visual system, a prototype of a cognitive system concerned with sensory perception, has specialized pathways for processing information about color, form, and movement. 1
Kandel; Principles of Neural Science 384 Radiological imaging techniques -- positron emission tomography (PET), magnetic resonance imaging (MRI), magnetoencephalopathy, and voltage-sensitive dyes. 0
Kandel; Principles of Neural Science 384 Network properties may not be identical or even similar to the properties of individual cells in the network. 0
Kandel; Principles of Neural Science 384 Personal space, the neural representation of the body surface. 0
Kandel; Principles of Neural Science 384 Peripersonal space, the space within arms reach. 0
Kandel; Principles of Neural Science 384 Extrapersonal space, the larger environment around the body. 0
Kandel; Principles of Neural Science 384 Representations of spatial relations and the association cortex of the posterior parietal lobe give rise to imagined and remembered space. 0
Kandel; Principles of Neural Science 385 In the cortical representation of space surrounding the body, the representation is not topographical but dynamic.  Representation is encoded into firing patterns of the cells that may not have any specific tomographic relation. 1
Kandel; Principles of Neural Science 387 Human somatosensory cortex was mapped by the neurosurgeon Wilder Penfield during operations for epilepsy. 2
Kandel; Principles of Neural Science 387 Somatic sensory and motor projection distortions in the cortex reflect differences in innervation density in the different areas of the body. 0
Kandel; Principles of Neural Science 387 Four fairly complete maps in the primary somatosensory cortex, one each in Brodmann areas 3a, 3b, 1 and 2. 0
Kandel; Principles of Neural Science 388 Clinical neurology has long been an accurate diagnostic discipline, even though for many decades it relied on only the simplest tools -- a wad of cotton, a safety pin, a tuning fork, and a reflex hammer. 1
Kandel; Principles of Neural Science 389 Magnetoencephalography can now be used to construct functional maps of the hand in normal subjects with a precision of millimeters. 1
Kandel; Principles of Neural Science 392 Primary somatosensory cortex projects to higher somatosensory areas of the anterior parietal lobe and to the multimodal association areas in the posterior parietal cortex (Brodmann's areas 5 and 7). 3
Kandel; Principles of Neural Science 392 Damage to the posterior parietal lobe produces agnosia, an inability to perceive objects. 0
Kandel; Principles of Neural Science 393 Agnosias most commonly seen with lesions in the right posterior parietal visuocortex are among the most remarkable that can be seen in neurological patients.  1
Kandel; Principles of Neural Science 393 Because the idea of having a left limb is completely foreign to them, patients may deny the existence of any paralysis in the limb and may attempt to leave the hospital prematurely, since they believe nothing is wrong with them. 0
Kandel; Principles of Neural Science 394 Memory of extra personal space is stored with a body-centered frame of reference. 1
Kandel; Principles of Neural Science 396 Consciousness derives from physical properties of the brain. 2
Kandel; Principles of Neural Science 400 Unity of consciousness -- our continuous and connected experience of events. 4
Kandel; Principles of Neural Science 400 Consciousness has many forms, e.g., the alert state. 0
Kandel; Principles of Neural Science 400 Activation of the thalamus and cortex by neurons of the brainstem and its reticular formation. 0
Kandel; Principles of Neural Science 400 Degrees of alertness (heightened attention, and difference, and attention, sleepiness) 0
Kandel; Principles of Neural Science 400 Major modulatory systems of the brainstem -- cholinergic,  dopaminergic, serotonergic, noradrenergic systems -- acting on the thalamus and cerebral cortex. 0
Kandel; Principles of Neural Science 400 Alertness can be general or focused, as when we selectively attend to one object in the external world to the exclusion of others. 0
Kandel; Principles of Neural Science 401 Parietal cortex contributes to selective attention to the location of objects in space. 1
Kandel; Principles of Neural Science 401 Selective attention enhances the responses of neurons in many brain areas, including neurons in the frontal cortex and superior colliculus. 0
Kandel; Principles of Neural Science 401 Francis Crick and Christof Koch have proposed that the attentional signals that modulate neurons in the visual system originate in the prefrontal cortex, the multimodal association areas concerned with planning and motor strategies. 0
Kandel; Principles of Neural Science 402 Representation of the body becomes related to the representation of visual space, whether actual, imagined, or remembered. 1
Kandel; Principles of Neural Science 402 Portions of the parietal lobe constitute the most distinctly human aspects of cortical organization. 0
Kandel; Principles of Neural Science 411 Coding of Sensory Information 9
Kandel; Principles of Neural Science 413 Sensory systems encode four elementary attributes of stimuli -- modality, location, intensity, and timing -- which are manifested in sensation. 2
Kandel; Principles of Neural Science 414 Since ancient times five major sensory modalities have been recognized -- vision, hearing, touch, taste, and smell. In addition to these classical senses we also consider the somatic senses of pain, temperature, itch, and proprioception (posture and movement of parts of the body) and vestibular sense of balance (the position of the body in the gravitational field). 1
Kandel; Principles of Neural Science 416 Each class of sensory receptors makes connections with distinctive structures in the central nervous system. 2
Kandel; Principles of Neural Science 416 Sensory systems comprise the somatosensory system, visual system, auditory system, vestibular system, olfactory system, and gustatory system. 0
Kandel; Principles of Neural Science 418 Spatial distribution of sensory neurons activated by a stimulus conveys information about the stimulus location. 2
Kandel; Principles of Neural Science 418 Receptive fields of sensory neurons in the somatosensory and visual systems defind the spatial resolution of the stimulus. 0
Kandel; Principles of Neural Science 419 Sensory neurons for hearing, taste, and smell are spatially organized according to sensitivity. 1
Kandel; Principles of Neural Science 419 Intensity of sensation is determined by the stimulus amplitude. 0
Kandel; Principles of Neural Science 421 Psychophysical laws govern the perception of stimulus intensity. 2
Kandel; Principles of Neural Science 421 Relationship between this stimulus strength and the intensity of sensation experienced by a person.   I = K log S/S0 0
Kandel; Principles of Neural Science 421 The intensity of sensation is best described by a power function rather than by a logarithmic relationship.                               I = K(S - S0)n 0
Kandel; Principles of Neural Science 421 Stimulus intensity is encoded by the frequency of action potentials in sensory nerves. 0
Kandel; Principles of Neural Science 423 The duration of sensation is determined in part by the adaptation rates of receptors. 2
Kandel; Principles of Neural Science 426 Sensory information is conveyed by populations of sensory neurons acting together. 3
Kandel; Principles of Neural Science 426 Sensory systems process information in a series of relay nuclei. 0
Kandel; Principles of Neural Science 427 Inhibitory interneurons within each relay nucleus help sharpen contrast between stimuli. 1
Kandel; Principles of Neural Science 428 The location and spatial dimensions of a stimulus are conveyed topographically, through each activated receptor's position in the sensory epithelium, called this receptive field. 1
Kandel; Principles of Neural Science 430 Bodily Senses 2
Kandel; Principles of Neural Science 430 Nerve transmits information from the receptor by modulation of the frequency of electrical impulses. 0
Kandel; Principles of Neural Science 430 Morphologically distinct receptors transduce particular forms of energy and transmit this information to the brain through nerve fibers dedicated to that modality. 0
Kandel; Principles of Neural Science 430 Pain is not the result of overstimulation of a generalized cutaneous receptor but results from electrical activity transmitted by specific sensory receptors called nociceptors. 0
Kandel; Principles of Neural Science 430 Somatic sensibility has four major modalities: (1) discriminative touch, (2) proprioception, (3) nociception, (4) temperature sense. 0
Kandel; Principles of Neural Science 431 Dorsal root ganglion neuron is a sensory receptor and the somatic sensory system. 1
Kandel; Principles of Neural Science 432 Touch is mediated by mechanoreceptors in the skin. 1
Kandel; Principles of Neural Science 432 Mechanoreceptors differ in morphology and skin location. 0
Kandel; Principles of Neural Science 432 Virtually all mechanoreceptors have specialized end organs    surrounding the nerve terminal. 0
Kandel; Principles of Neural Science 436 Two-point discrimination varies throughout the body surface (diagram) 4
Kandel; Principles of Neural Science 436 Spatial resolution of stimuli on the skin    varies throughout the body because the density of mechanoreceptors varies. 0
Kandel; Principles of Neural Science 437 Vibration sense is coded by spike trains and mechanoreceptors in the skin. (diagram) 1
Kandel; Principles of Neural Science 438 Spatial characteristics of objects are signaled by populations of mechanoreceptors. 1
Kandel; Principles of Neural Science 441 Warmth and cold are mediated by thermal receptors. 3
Kandel; Principles of Neural Science 442 Pain is mediated by nociceptors. 1
Kandel; Principles of Neural Science 443 Proprioception is mediated by mechanoreceptors in skeletal muscle and joint capsules. 1
Kandel; Principles of Neural Science 443 Viscera have mechanosensory and chemosensory receptors. 0
Kandel; Principles of Neural Science 444 Mechanoreceptors and proprioceptors are innervated by large-diameter myelinated axons whereas thermal receptors and  nociceptors are small myelinated or unmyelinated axons. 1
Kandel; Principles of Neural Science 444 Fiber size affects the speed at which action potentials are conducted to the brain. 0
Kandel; Principles of Neural Science 444 Large fibers conduct action potentials more rapidly because the internal resistance to current flow along the axon is low and the nodes of Ranvier are far more widely spaced along the length. 0
444 Conduction velocity;  m/sec,  mm/ms 0
Kandel; Principles of Neural Science 444 Myelinated:  (large, 72-120), (medium 36-72), (small 4-36) 0
Kandel; Principles of Neural Science 444 Unmyelinated:  (0.4-2.0) 0
Kandel; Principles of Neural Science 445 Distribution of dermatomes (diagram) 1
Kandel; Principles of Neural Science 445 Dermatome maps are an important diagnostic tool for locating the site of injury to the spinal cord and dorsal roots. 0
Kandel; Principles of Neural Science 445 31 pairs of dorsal roots are labeled by the corresponding vertebral foramen through which the root enters the spinal cord. 0
Kandel; Principles of Neural Science 445 Facial skin is innervated by the three branches of the trigeminal nerve. 0
Kandel; Principles of Neural Science 446 Large fiber neuropathy, selective loss of axons, diabetes, large sensory fibers degenerate. 1
Kandel; Principles of Neural Science 446 Topographic arrangement of receptors in the skin is preserved as the central processes of the dorsal root ganglion neurons enter the spinal cord through the  dorsal roots. 0
Kandel; Principles of Neural Science 446 Upon entry to the spinal cord the central axons of dorsal root ganglion neurons branch extensively and project to nuclei in spinal gray matter and brainstem. 0
Kandel; Principles of Neural Science 446 Sensory specialization of dorsal root ganglion neurons is preserved in the central nervous system through distinct ascending pathways for the various somatic modalities. 0
Kandel; Principles of Neural Science 448 Crossing of fibers in the medulla and pons.  Right side of the brain receives sensory information from the limbs and trunk on the left side of the body. 2
Kandel; Principles of Neural Science 448 Input from the legs are located most laterally, while those from the arm are located more medially.  Inputs from the face are most medial. 0
Kandel; Principles of Neural Science 451 Touch 3
Kandel; Principles of Neural Science 458 Columnar organization of cortical neurons is a consequence of the pattern of connections between neurons in different layers of cortex. 7
Kandel; Principles of Neural Science 472 Perception of Pain 14
Kandel; Principles of Neural Science 472 Pain -- pricking, burning, aching, stinging, soreness. 0
Kandel; Principles of Neural Science 472 Pain is a percept. 0
Kandel; Principles of Neural Science 473 Highly individual and subjective nature of pain.  There are no painful stimuli -- stimuli that invariably elicit the perception of pain in all individuals. 1
Kandel; Principles of Neural Science 473 Many wounded soldiers do not feel pain until thery are safely remove from battle.  Athletes often do not detect their injuries and until their game is over. 0
Kandel; Principles of Neural Science 473 Pain can be persistent or chronic.  Persistent pain characterizes many clinical conditions and is a major reason why patients seek medical attention, whereas chronic pain appears to serve no useful purpose; it only makes patients miserable. 0
Kandel; Principles of Neural Science 473 Persistent pain can be subdivided into two broad classes, nociceptive and neuropathic. 0
Kandel; Principles of Neural Science 473 Nociceptive pains result from the direct activation of nociceptors in the skin and soft tissues in response to tissue injury and usually arise from accompanying inflammation. 0
Kandel; Principles of Neural Science 473 Sprains and strains produce mild forms of nociceptive pain, whereas the pain of arthritis or a tumor that invades soft tissue is much more severe. 0
Kandel; Principles of Neural Science 473 Neuropathic pains result from direct injury to nerves in the peripheral or central nervous systems and often have a burning or electric sensation. 0
Kandel; Principles of Neural Science 473 Neuropathic pains  include the severe pain that occurs in some patients after a bout of shingles. 0
Kandel; Principles of Neural Science 473 Three major classes of nociceptors -- thermal, mechanical, polymodal. 0
Kandel; Principles of Neural Science 474 The three classes of nociceptors are widely distributed in the skin and deep tissues. 1
Kandel; Principles of Neural Science 477 Neuropeptides enhance and prolong the actions of glutamate. 3
Kandel; Principles of Neural Science 477 Actions of glutamate released from sensory terminals are confined to postsynaptic neurons in the immediate vicinity of the synaptic terminals as a result of the efficient reuptake of amino acids into glial cells or nerve terminals. 0
Kandel; Principles of Neural Science 477 Neuropeptides released from sensory terminals can diffuse considerable distances from their site of release because there is no specific reupdate mechanism. 0
Kandel; Principles of Neural Science 477 Release of neuropeptides from a single afferent fiber are likely to influence many postsynaptic dorsal horn neurons. 0
Kandel; Principles of Neural Science 477 Peptide actions contribute both to the excitability of dorsal horn neurons and to the unlocalized character of many pain conditions. 0
Kandel; Principles of Neural Science 477 Sensitization -- repeated application of noxious mechanical stimuli to nearby nociceptors that were previously unresponsive. 0
Kandel; Principles of Neural Science 477 Sensitization of nociceptors after injury or inflammation results from the release of a variety of chemicals by the damaged cells and tissues in the vicinity of the injury.  The chemicals act to decrease the threshold for activation of nociceptors. 0
Kandel; Principles of Neural Science 478 Aspirin and other nonsteroidal anti-inflammatory analgesics. 1
Kandel; Principles of Neural Science 478 Cardinal signs of inflammation -- heat (calor), redness (rubor), swelling (tumor). 0
Kandel; Principles of Neural Science 478 Heat and redness are produced by the dilation of peripheral blood vessels, whereas swelling results from plasma extravasation. 0
Kandel; Principles of Neural Science 481 Cingulate gyrus is part of the limbic system and is thought to be involved in processing the emotional component of pain. 3
Kandel; Principles of Neural Science 482 Neurons in the insular cortex process information on the internal state of the body. 1
Kandel; Principles of Neural Science 482 Insular cortex may integrate the sensory, affective, and cognitive components. 0
Kandel; Principles of Neural Science 483 Opium poppy -- opiates such as morphine and codeine are effective analgesic agents. 1
Kandel; Principles of Neural Science 489 Repeated use of morphine to relieve pain can cause patients to develop increasing resistance to the effects of the drug, so that progressively higher doses are required to achieve the same analgesic effect. 6
Kandel; Principles of Neural Science 489 Addiction refers to psychological craving. 0
Kandel; Principles of Neural Science 489 Psychological addiction almost never occurs when morphine is used to treat chronic pain. 0
Kandel; Principles of Neural Science 489 Soldiers wounded in battle and athletes injured in sporting events report that they do not feel pain. 0
Kandel; Principles of Neural Science 490 Pain is dependent on experience and varies from person to person. 1
Kandel; Principles of Neural Science 492 Constructing the Visual Image 2
Kandel; Principles of Neural Science 507 Visual Processing by the Retina 15
Kandel; Principles of Neural Science 523 Central Visual Pathways 16
Kandel; Principles of Neural Science 526 Superior colliculus controls saccadic eye movements. 3
Kandel; Principles of Neural Science 527 Saccadic eye movements -- shift the gaze rapidly from one point in the visual scene to another. 1
Kandel; Principles of Neural Science 527 Control of a saccadic eye movements is thought to be controlled by inputs from the cerebral cortex. 0
Kandel; Principles of Neural Science 529 Lateral geniculate nucleus is the principal subcortical site for processing visual information. 2
Kandel; Principles of Neural Science 548 Perception of Motion, Depth, and Form 19
Kandel; Principles of Neural Science 550 Separate pathways to the temporal and parietal cortices course through the extrastriate cortex beginning in V2. (diagram) 2
Kandel; Principles of Neural Science 553 Middle temporal area (MT) appears to be devoted to motion processing. 3
Kandel; Principles of Neural Science 553 MT has a retinotopic map of the contralateral visual field, but the receptive fields of cells within this map are about 10 times wider than those of cells in the striate cortex. 0
Kandel; Principles of Neural Science 553 Cells with similar directional specificity are organized into vertical columns, running from the surface of the cortex to the white matter. 0
Kandel; Principles of Neural Science 553 In the human brain, an area devoted to motion has been identified at the junction of the parietal, temporal, and occipital cortices. 0
Kandel; Principles of Neural Science 565 The limited capacity of the visual system means that at any given time only a fraction of the information available from the two retinas can be processed. 12
Kandel; Principles of Neural Science 565 Selective filtering of visual information is achieved by visual attention. 0
Kandel; Principles of Neural Science 565 Posterior parietal cortex, a region known from clinical studies to be involved in attention. 0
Kandel; Principles of Neural Science 566 Binding problem and visual system 1
Kandel; Principles of Neural Science 566 Information about motion, depth, form, and color is processed in many different visual areas and organized into at least two cortical pathways. 0
Kandel; Principles of Neural Science 566 Complex visual images are built up at successively higher processing centers. 0
Kandel; Principles of Neural Science 566 Binding problem -- how consciousness of an ongoing, coherent experience emerges from the information processing being conducted independently in different cortical areas. 0
Kandel; Principles of Neural Science 566 Associative process by which multiple features of one object are brought together in a coherent percept requires attention. 0
Kandel; Principles of Neural Science 567 Neurons have larger and larger receptive fields at higher levels in the cortical visual pathways. 1
Kandel; Principles of Neural Science 567 Wolfgang Singer and colleagues.  When an object activates a population of neurons in the visual cortex, the neurons tend to oscillate and fire in unison. These oscillations indicate a synchrony among cells, which could bind together the activity of cells responding to different features of an object. 0
Kandel; Principles of Neural Science 567 Barry Richmond and colleagues. Neurons extending from the LGN to the inferior temporal cortex convey information in the temporal pattern of the spikes. 0
Kandel; Principles of Neural Science 567 Cells in different areas all convey some information about a number of stimulus features, but different cells carry comparatively more or less about each feature. 0
Kandel; Principles of Neural Science 568 Dorsal pathway extends from V1, through areas MT and MST, to the posterior parietal cortex. 1
Kandel; Principles of Neural Science 568 Ventral pathway extends from V1, through V4, to the inferior temporal cortex. 0
Kandel; Principles of Neural Science 568 Dorsal or posterior parietal pathway is concerned with determining where an object is. 0
Kandel; Principles of Neural Science 568 Ventral or inferior temporal pathway is involved in recognizing what the object is. 0
Kandel; Principles of Neural Science 568 Motion and depth information in the dorsal posterior parietal pathway and on form perception in the ventral inferior temporal pathway.  Both pathways represent hierarchies for visual processing that lead to greater abstraction at successive levels. 0
Kandel; Principles of Neural Science 572 Color Vision 4
Kandel; Principles of Neural Science 590 Hearing 18
Kandel; Principles of Neural Science 590 Human hearing commences when the cochlea, a snail shaped receptor organ, of the inner ear, transducers sound energy into electrical signals. 0
Kandel; Principles of Neural Science 590 Cochlea contain cellular amplifiers that augment our auditory sensitivity and are responsible for the first stages of frequency analysis. 0
Kandel; Principles of Neural Science 590 Each of the paired cochleas contains slightly more than 30,000 reset the hair cells. 0
Kandel; Principles of Neural Science 590 Damage to or deterioration of the hairs cells accounts for most of the hearing loss in the nearly 30,000,000 Americans who are afflicted with significant deafness. 0
Kandel; Principles of Neural Science 590 Information flows from the cochlea to the brainstem through a richly interconnected series of nuclei. 0
Kandel; Principles of Neural Science 590 Brain stem components of the auditory pathway are essential for localizing sound sources and suppressing the effects of echoes. 0
Kandel; Principles of Neural Science 591 Auditory regions of the cerebral cortex further analyze auditory information and deconstruct complex sound patterns such as human speech. 1
Kandel; Principles of Neural Science 591 The ear has three functional parts -- external ear,    middle ear,    inner ear. 0
Kandel; Principles of Neural Science 591 Our capacity to localize sounds in space, especially along the vertical axis, depends critically abundant sound gathering properties of the external ear. 0
Kandel; Principles of Neural Science 591 The middle ear is an air-filled pouch extending from the pharynx, to which it is connected by the eustachian tube. 0
Kandel; Principles of Neural Science 591 Mechanical energy derived from airborne sound progresses across the middle ear as motions of three tiny ossicles, or bones -- the malleus, or hammer; the incus, or anvil; the stapes, or stirrup. 0
Kandel; Principles of Neural Science 591 The base of the malleus is attached to the tympanic membrane. 0
Kandel; Principles of Neural Science 592 The flattened termination of the stapes, the footplate, inserts in an opening -- the overall window -- in the bony covering of the cochlear. 1
Kandel; Principles of Neural Science 592 The first two ossicles of the middle ear are relics of evolution, for their antecedents served as components the jaw of reptilian ancestors. 0
Kandel; Principles of Neural Science 592 Human cochlear consists of a progressively diminishing diameter conical structure like a snail's shell. 0
Kandel; Principles of Neural Science 592 Each cochlea is about 9 mm across. 0
Kandel; Principles of Neural Science 592 The interior of the cochlea consists of three fluid filled tubes wound helically. 0
Kandel; Principles of Neural Science 592 The basilar membrane, which forms the partition between the scala media and its subjacent scale tympani, is a complex structure upon which auditory transduction occurs. 0
Kandel; Principles of Neural Science 593 Weber-Fechner law -- we perceive sound logarithmically with the increase in sound pressure level. 1
Kandel; Principles of Neural Science 593 0 dB SPL is defined as the sound pressure whose rms value is 20 mPa, corresponding to the approximate threshold of human hearing at 4 kHz, the frequency at which our ears are most sensitive. 0
Kandel; Principles of Neural Science 593 The loudest sound tolerable to humans, with an intensity of about 120 dB SPL, transiently alters the local atmospheric pressure (about 105 Pa) by much less than 0.1%. 0
Kandel; Principles of Neural Science 593 Sound pressure waves impinge upon the tympanum, displacing the malleus, which is fixed to the inner surface of the eardrum. 0
Kandel; Principles of Neural Science 593 The motions of the ossicles are complex, depending upon both the frequency and intensity of sound. The action of these bones may be understood as two interconnected levers, the malleus and incus, and a piston, the stapes. 0
Kandel; Principles of Neural Science 593 This stapes footplate serves as a piston that pushes and pulls cyclically upon the fluid in the scala vestibuli. 0
Kandel; Principles of Neural Science 593 Conductive hearing loss by the ossicles is important because surgical intervention is highly effective. 0
Kandel; Principles of Neural Science 593 Functional Anatomy of the Cochlea 0
Kandel; Principles of Neural Science 593 Basilar membrane is a mechanical analyzer of sound frequency. 0
Kandel; Principles of Neural Science 593 The mechanical properties of the basilar membrane are key to the cochlea's operation. 0
Kandel; Principles of Neural Science 593 Suppose that the basilar membrane had uniform dimensions and mechanical properties along its entire length, about 33 mm. This simple form of basilar membrane occurs in the auditory organs of some reptiles and birds. 0
Kandel; Principles of Neural Science 594 The critical characteristic of the basilar membrane and in mammalian clock is that it is not uniform. 1
Kandel; Principles of Neural Science 594 The basilar membrane's    mechanical properties    vary continuously along the cochlea's length. 0
Kandel; Principles of Neural Science 594 The cochlea chambers become progressively larger from the organ's apex toward its base. 0
Kandel; Principles of Neural Science 594 The basilar membrane is relatively thin and floppy at the apex of the cochlea but thicker and more taut toward the base. 0
Kandel; Principles of Neural Science 594 Because of the systematic variation in mechanical properties along the basilar membrane, stimulation with a pure tone evokes the greatest amplitude at a particular position. 0
Kandel; Principles of Neural Science 594 A traveling wave of asending the basilar membrane, reaches its maximum amplitude at the position appropriate for the frequency of stimulation, then rapidly declines in size as it advances toward the cochlea apex. 0
Kandel; Principles of Neural Science 594 The energy that evokes movement in each segment of the basal membrane comes from motion of the fluid masses above and below the membrane. 0
Kandel; Principles of Neural Science 594 The mammalian basal membrane is tuned to a progression of frequencies along its length. 0
Kandel; Principles of Neural Science 594 At the apex of the human cochlea the partition responds best to the lowest frequencies that we can hear, down to approximately 20 Hz. 0
Kandel; Principles of Neural Science 594 The basilar membrane at the cochlea base responds to frequencies as great as 20 kHz. 0
Kandel; Principles of Neural Science 594 Intervening frequencies are represented along the basilar membrane and a continuous array. 0
Kandel; Principles of Neural Science 594 The cochlea deconstructs sounds    by confining the action    of each component tone    to a discrete segment of the basilar membrane. 0
Kandel; Principles of Neural Science 594 The arrangement of vibration frequencies in the basilar membrane is an example of tonotopic map. 0
Kandel; Principles of Neural Science 594 The relation between characteristic frequency    and position along the basilar membrane    varies smoothly and monotonically    but is not linear. 0
Kandel; Principles of Neural Science 594 The logarithm of the best frequency is roughly proportional to the distance from the cochlea's apex. 0
Kandel; Principles of Neural Science 594 A vowel sound in human speech ordinarily comprises, at any instant, three dominant frequency components. 0
Kandel; Principles of Neural Science 597 Each traveling wave of sound reaches its peak excursion    at the basal membrane position    appropriate for the relative frequency component. 3
Kandel; Principles of Neural Science 597 The basal membrane acts as a mechanical frequency analyzer    by distributing stimulus energy to the hair cells arrayed along its length    according to the various pure tones that make up the stimulus. 0
Kandel; Principles of Neural Science 597 The basal membrane's    pattern of motion    begins the encoding of the frequencies and intensities in a sound. 0
Kandel; Principles of Neural Science 597 The organ of Corti is the receptor organ of the inner ear, containing the hair cells and a variety of supporting cells. 0
Kandel; Principles of Neural Science 597 The organ of Corti appears as an epithelial ridge extending along the length of the basalar membrane. 0
Kandel; Principles of Neural Science 597 The approximately 16,000 hairs cells in each cochlea are innervated by about 30,000 afferent nerve fibers, which carry information into the brain along the eighth cranial nerve. 0
Kandel; Principles of Neural Science 597 Both the hair cells and the auditory nerve fibers are tonotopically organized. 0
Kandel; Principles of Neural Science 597 At any position along the basilar membrane, the hair cells are optimally sensitive to a particular frequency,    and these frequencies are logarithmically mapped in ascsending order from the cochlea's apex to its base. 0
Kandel; Principles of Neural Science 597 The organ of Corti includes a wealth of cell types, most of obscure function. 0
Kandel; Principles of Neural Science 598 Every hair cell is most sensitive to stimulation at a specific frequency. 1
Kandel; Principles of Neural Science 598 On average, successive inner hair cells    differ in characteristic frequency    by about 0.2%. 0
Kandel; Principles of Neural Science 599 A traveling wave    evoked even by a pure sinusoidal stimulus    spreads appreciably    along the basalar membrane. 1
Kandel; Principles of Neural Science 599 The tuning curve is a graph of sound intensity, presented logarithmically in decibels of sound pressure level, against stimulus frequency. 0
Kandel; Principles of Neural Science 599 Sound energy is mechanically amplified in the cochlea. 0
Kandel; Principles of Neural Science 599 A large portion of the energy in an acoustical stimulus must go into overcoming the damping effects of cochlea fluid on basilar membrane motion rather than into excitation of hair cells. 0
Kandel; Principles of Neural Science 599 The sensitivity of the cochlea is too great, and auditory frequency selectivity to sharp, to result solely from the inner ear's passive mechanical properties. The cochlea must have some active means of amplifying sound energy. 0
Kandel; Principles of Neural Science 599 One indication that    amplification occurs in the cochlea    comes from experimental results that show that the motion of the basil  membrane    is augmented over 100-fold during low intensity stimulation,    but that this effect diminishes progressively as the stimulus grows in strength. 0
Kandel; Principles of Neural Science 599 Inner ear's performance requires amplification. 0
Kandel; Principles of Neural Science 601 Neural Processing of Auditory Information 2
Kandel; Principles of Neural Science 601 Ganglion cells innervate cochlear hair cells. 0
Kandel; Principles of Neural Science 601 Information flows from the cochlear hair cells to neurons whose cell bodies lie in the cochlea ganglion. 0
Kandel; Principles of Neural Science 601 About 30,000 ganglion cells innervate the hair cells of each inner ear. 0
Kandel; Principles of Neural Science 601 At least 90% of the cochlea ganglion cells terminate on inner hair cells. 0
Kandel; Principles of Neural Science 601 Each cochlea ganglion cell axon    innervates only a single hair cell,    but each hair cell direct its output to several nerve fibers, on average nearly 10. 0
Kandel; Principles of Neural Science 601 The neural information from which hearing arises originates almost entirely at inner hair cells, which dominate the input to cochlea ganglion cells. 0
Kandel; Principles of Neural Science 601 The output of each and her hair cell is sampled by many nerve fibers, which independently encode information about the frequency and intensity of sound. 0
Kandel; Principles of Neural Science 601 Each hair cell forwards information of somewhat differing nature to the brain along separate axons. 0
Kandel; Principles of Neural Science 601 At any point along the cochlear spiral,    or any position within the spiral ganglion,    neurons respond best to stimulation at the characteristic frequency of the contiguous hair cells. 0
Kandel; Principles of Neural Science 601 The tonotopic organization of the auditory neural pathways does begin at the earliest possible site, and immediately postsynaptic to inner hair cells. 0
Kandel; Principles of Neural Science 601 Relatively few cochlea ganglion cells    innervate outer hair cells. 0
Kandel; Principles of Neural Science 601 Cochlea nerve fibers    encode stimulus frequency and intensity. 0
Kandel; Principles of Neural Science 601 Each axon in the cochlear nerve is most responsive to stimulation at a particular frequency of sound. 0
Kandel; Principles of Neural Science 601 The acoustic sensitivity of axons in the cochlear nerve    mirrors the innervation pattern of spiral ganglion cells. 0
Kandel; Principles of Neural Science 603 Sound processing begins in the cochlear nuclei. 2
Kandel; Principles of Neural Science 603 Each auditory nerve fiber    branches    as it enters the brain stem. 0
Kandel; Principles of Neural Science 603 Each of the three cochlea nuclei is tonotopically organized; cells with progressively higher characteristic frequencies are arrayed in orderly progression along one axis of the structure. 0
Kandel; Principles of Neural Science 604 Central auditory pathways extend from the cochlear nucleus to the auditory cortex.  (diagram) 1
Kandel; Principles of Neural Science 606 Relay nuclei in the brainstem mediate localization of sound sources. 2
Kandel; Principles of Neural Science 608 The medial geniculate nucleus constitutes the thalamic relay of the auditory system. 2
Kandel; Principles of Neural Science 608 Medial geniculate nucleus is organized tonotopically. 0
Kandel; Principles of Neural Science 608 In the medial geniculate nucleus most cells are sharply tuned to specific stimulus frequencies,    and most are responsive to stimulation through either ear. 0
Kandel; Principles of Neural Science 608 Sensitivity to interaural time or intensity difference is a property first elaborated in the interior colliculus. 0
Kandel; Principles of Neural Science 608 Auditory information is processed in multiple areas of the cerebral cortex. 0
Kandel; Principles of Neural Science 608 The ascending auditory pathway    terminates    in the cerebral cortex,    where several distinct auditory areas occur on the dorsal surface of the temporal lobe. 0
Kandel; Principles of Neural Science 609 The most prominent projection from the principal nucleus of the medial geniculate nucleus    extends to the primary audio cortex (Brodmann areas 41 and 42) on the transverse gyrus of Heschl. 1
Kandel; Principles of Neural Science 609 The cytoarchitectonically distinct region contains a tonotopic representation of characteristic frequencies;    neurons tuned to low frequencies occur in the rostral end of the area,    while the caudal region includes cells responsive to high frequencies. 0
Kandel; Principles of Neural Science 609 The parallel processing and conformal mapping of the auditory cortex    resembles the somatosensory and visual cortices. 0
Kandel; Principles of Neural Science 609 Although most neurons in the primary auditory cortex are responsive to stimulation through either ear, their sensitivities are not identical. 0
Kandel; Principles of Neural Science 609 It is highly probable that the human auditory cortex is subdivided into numerous functional areas, but the positions and roles of such areas remain to be determined. 0
Kandel; Principles of Neural Science 614 Sensory transduction in the Ear 5
Kandel; Principles of Neural Science 625 Smell and Taste: Chemical Senses 11
Kandel; Principles of Neural Science 653 Organization of Movement 28
Kandel; Principles of Neural Science 653 Brain constructs internal representations of the world by integrating information from the different sensory systems. 0
Kandel; Principles of Neural Science 653 Motor systems of the brain and spinal cord allow us to maintain balance and posture and to communicate through speech and gesture. 0
Kandel; Principles of Neural Science 653 The pirouette of a ballet dancer, the powered backhand of a tennis player, the fingering technique of the pianist, and the coordinated eye movements of a reader all require a remarkable degree of motor skill. 0
Kandel; Principles of Neural Science 653 After a period of training, the brain's motor systems execute motor programs with ease, for the most part automatically. 0
Kandel; Principles of Neural Science 654 Conscious processes are not necessary for the moment-to-moment control of movement. 1
Kandel; Principles of Neural Science 654 Vision supplies critical cognitive information about the location and shape of objects. 0
Kandel; Principles of Neural Science 654 Loss of vestibular input impairs the ability to maintain balance and orientation. 0
Kandel; Principles of Neural Science 654 Components of the motor systems are organized hierarchically. 0
Kandel; Principles of Neural Science 654 Relatively automatic behaviors include rhythmic behaviors, such as breathing or running as well as reflexes, such as knee-jerk or coughing. 0
Kandel; Principles of Neural Science 654 Reflexes and automatic rhythmic movements are stereotyped, in contrast to the endless varieties of voluntary movements. 0
Kandel; Principles of Neural Science 654 Spinal cord contains local circuits that coordinate reflexes, and these same circuits participate in more complex voluntary movements governed by higher brain centers. 0
Kandel; Principles of Neural Science 654 Three distinct categories of movement: (1) reflexive, (2) rhythmic, and (3) voluntary. 0
Kandel; Principles of Neural Science 654 Reflexes are involuntary coordinated patterns of muscle contraction and relaxation elicited by peripheral stimuli. 0
Kandel; Principles of Neural Science 654 Receptors in muscles produce stretch reflex whereas cutaneous receptors produce withdrawal reflexes. 0
Kandel; Principles of Neural Science 656 Repetitive arrhythmic motor patterns include chewing, swallowing, and scratching. 2
Kandel; Principles of Neural Science 656 Circuits for repetitive rhythmic motor patterns lie in the spinal cord and brain stem. 0
Kandel; Principles of Neural Science 656 Moment-to-moment control is called feedback. 0
Kandel; Principles of Neural Science 656 Anticipatory mode is called feed-forward control.  Detect imminent perturbations and initiate proactive strategies based on experience. 0
Kandel; Principles of Neural Science 657 Very sensitive mechanicoreceptors in muscles. 1
Kandel; Principles of Neural Science 657 Cutaneous afferents in the fingertips provide critical feedback signals. 0
Kandel; Principles of Neural Science 657 Feed-forward control is widely used by motor systems to control posture and movement. 0
Kandel; Principles of Neural Science 657 Catching a ball is a visually triggered feet-forward response,  predicting balls path. 0
Kandel; Principles of Neural Science 657 Spinal circuits can mediate rapid feedback adjustments. 0
Kandel; Principles of Neural Science 657 Feed-forward control is essential for rapid action. 0
Kandel; Principles of Neural Science 659 Motor program is a representation of the plan for movement. 2
Kandel; Principles of Neural Science 660 Nervous system deconstructs complex actions into elemental movements that have highly stereotyped spatial and temporal characteristics. 1
Kandel; Principles of Neural Science 661 Simple spatiotemporal elements of a movement are called  movement primitives or movements schemas. 1
Kandel; Principles of Neural Science 661 Voluntary reaction times are significantly longer than the latencies of reflex responses. 0
Kandel; Principles of Neural Science 661 Voluntary responses to proprioceptive stimuli range from 80 to 120 ms. 0
Kandel; Principles of Neural Science 661 Shortest latency for monosynaptic reflex response to muscle stretches is only about 40 ms. 0
Kandel; Principles of Neural Science 661 Longer response time for the voluntary response results from the additional synapses interposed between afferent input and motor output. 0
Kandel; Principles of Neural Science 661 Reactions to visual stimuli require more time (150-180 ms), because of the larger number of synaptic relays in the retina. 0
Kandel; Principles of Neural Science 661 Summation time of synapses is highly variable. 0
Kandel; Principles of Neural Science 661 Reaction time increases systematically with the number of choices available. 0
Kandel; Principles of Neural Science 661 For complex tasks, reaction times are half a second to a second. 0
Kandel; Principles of Neural Science 661 Voluntary responses are processed in stages, including a step in which appropriate response is selected from among alternatives. 0
Kandel; Principles of Neural Science 663 Processing of sensory inputs and commands to motor neurons and muscles is distributed in hierarchically interconnected areas of the spinal cord, brain stem, and forebrain. 2
Kandel; Principles of Neural Science 663 Each level of the hierarchy has circuits that can, through their input and output connections, organize or regulate complex motor responses. 0
Kandel; Principles of Neural Science 663 Sensory information relating to movement is processed in different systems that operate in parallel. 0
Kandel; Principles of Neural Science 663 Spinal cord is the lowest level in the hierarchical organization. It contains the neuronal circuits that mediate a variety of reflexes and rhythmic automatisms such as locomotion and scratching. 0
Kandel; Principles of Neural Science 663 Reflex movements of the face and mouth are located in the brain stem. 0
Kandel; Principles of Neural Science 663 Simplest neural circuits are monosynaptic, includes only the primary sensory neuron and the motor neuron. 0
Kandel; Principles of Neural Science 663 Most reflexes are mediated by polysynaptic circuits, where one or more interneurons are interposed between the primary sensory neuron and the motor neuron. 0
Kandel; Principles of Neural Science 663 Interneurons and motor neurons also receive input from axons descending from higher centers. 0
Kandel; Principles of Neural Science 663 Supraspinal signals can modify reflex responses to peripheral stimuli by facilitating or inhibiting different populations of interneurons. 0
Kandel; Principles of Neural Science 663 Supraspinal signals also coordinate motor actions through interneurons. 0
Kandel; Principles of Neural Science 663 All motor commands eventually converge on motor neurons, whose axons exit the spinal cord or brain stem to innervate skeletal muscles. 0
Kandel; Principles of Neural Science 663 The next level above the spinal cord in the motor hierarchy is in the brain stem. 0
Kandel; Principles of Neural Science 663 Cortex is the highest level of motor control. 0
Kandel; Principles of Neural Science 663 Primary motor cortex and several premotor areas project directly to the spinal cord and also regulate motor tracks that originate in the brain stem. 0
Kandel; Principles of Neural Science 663 Premotor areas are important for coordinating and planning complex sequences of movement. 0
Kandel; Principles of Neural Science 663 Premotor areas receive information from the posterior parietal and prefrontal association cortices and project to the primary motor cortex as well as to the spinal cord. 0
Kandel; Principles of Neural Science 663 The variety of reflex circuits in the spinal cord and brain stem simplifies the instructions the cortex must send the lower levels. 0
Kandel; Principles of Neural Science 663 By facilitating some circuits and inhibiting others, higher levels can let sensory inputs at lower levels govern the temporal details of an evolving movement. 0
Kandel; Principles of Neural Science 663 Patterns of coordination in spinal circuits are relatively stereotyped. 0
Kandel; Principles of Neural Science 663 Cerebellum and basal ganglia influence cortical and brainstem motor systems. 0
Kandel; Principles of Neural Science 663 Cerebellum and basal ganglia provide feedback circuits that regulate cortical and brainstem motor areas.  They receive inputs from various areas of cortex and project to motor areas of the cortex via the thalamus. 0
Kandel; Principles of Neural Science 663 Loop circuits of the basal ganglia and cerebellum flow through separate regions of the thalamus to different cortical areas. 0
Kandel; Principles of Neural Science 665 Inputs to the basal ganglia and cerebellum from the cortex are separate. 2
Kandel; Principles of Neural Science 665 Cerebellum and basal ganglia do not send significant output to the spinal cord, but they do act directly on projection neurons in the brainstem. 0
Kandel; Principles of Neural Science 665 Basal ganglia have increasingly been implicated in motivation and the selection of adaptive behavioral plans. 0
Kandel; Principles of Neural Science 665 Cerebellum circuits are involved with the timing and coordination of movements in progress and with the learning of motor skills. 0
Kandel; Principles of Neural Science 666 Release phenomena are abnormal and stereotyped responses that are explained by the withdrawal of tonic inhibition from neuronal circuits mediating a behavior. 1
Kandel; Principles of Neural Science 668 Brain stem contains, in addition to the motor nuclei that regulate the facial muscles, many groups of neurons that project to the spinal gray matter. 2
Kandel; Principles of Neural Science 671 Primary motor cortex lies in the precentral gyrus in Brodmann's area 4. 3
Kandel; Principles of Neural Science 671 Axons of cortical neurons that project to the spinal cord run together in the corticospinal tract, a massive bundle fibers containing about 1 million axons. 0
Kandel; Principles of Neural Science 671 About a third of the corticospinal fibers originate from the precentral gyrus of the frontal lobe; another third originate from area 6, the rest originate in areas 3, 2, and 1 in the somatic sensory cortex. 0
Kandel; Principles of Neural Science 671 Medullary pyramid, a conspicuous landmark on the ventral surface of the medulla. 0
Kandel; Principles of Neural Science 671 Corticobulbar fibers that control muscles of the head and face terminate in motor and sensory (cranial nerve) nuclei in the brain stem. 0
Kandel; Principles of Neural Science 671 In humans, corticobulbar fibers form monosynaptic connections with motor neurons in the trigeminal, facial, and hypocolossal nuclei. 0
Kandel; Principles of Neural Science 671 Movements of the eyes are controlled by a different system. 0
Kandel; Principles of Neural Science 671 Major cortical inputs to the motor areas of cortex are from the prefrontal, parietal, and temporal association areas. 0
Kandel; Principles of Neural Science 671 Major subcortical input to the motor cortical areas comes from the thalamus where separate nuclei convey inputs from the basal ganglia and cerebellum. 0
Kandel; Principles of Neural Science 671 Spinal reflexes show that the spinal cord contains neural circuits for generating simple and coordinated movements. 0
Kandel; Principles of Neural Science 672 Motor commands are organized hierarchically. 1
Kandel; Principles of Neural Science 672 Brain stem integrates spinal reflexes into a variety of automated movements that control posture and locomotion. 0
Kandel; Principles of Neural Science 672 Several interconnected areas of cortex that project to the descending systems of the brainstem and spinal cord initiate and control complex voluntary movements. 0
Kandel; Principles of Neural Science 672 Somatotopic map of the body -- somatotopic organization is preserved in the outputs of each component. 0
Kandel; Principles of Neural Science 672 Each level of motor control receives peripheral sensory information that is used to modify the motor output at that level. 0
Kandel; Principles of Neural Science 672 Motor programs are refined continuously by learning. 0
Kandel; Principles of Neural Science 674 Motor unit and Muscle action 2
Kandel; Principles of Neural Science 695 Diseases of the Motor unit 21
Kandel; Principles of Neural Science 713 Spinal Reflexes 18
Kandel; Principles of Neural Science 737 Locomotion 24
Kandel; Principles of Neural Science 756 Voluntary movement 19
Kandel; Principles of Neural Science 760 Supplementary motor area -- medial parts of areas 6. 4
Kandel; Principles of Neural Science 768 When a particular finger is moved, digit neurons are dispersed throughout the hand control area of primary motor cortex. The manner in which the activity is coordinated to produce a finger movement is analogous to population coding. 8
Kandel; Principles of Neural Science 779 Planning and execution of voluntary movement relies on sensorimotor transformations in which representations of the external environment are integrated into motor programs. 11
Kandel; Principles of Neural Science 782 Control of gaze 3
Kandel; Principles of Neural Science 784 Saccadic system points the fovea toward objects of interest. 2
Kandel; Principles of Neural Science 784 Eyes explore the world in a series of active fixations connected by saccades. 0
Kandel; Principles of Neural Science 784 Saccades are highly stereotyped. 0
Kandel; Principles of Neural Science 784 Saccades are extremely fast, occurring within a fraction of a second, at speeds up to 900°/s. 0
Kandel; Principles of Neural Science 784 Distance of the target from the fovea determines the velocity of a saccadic eye movement.  We can change the amplitude and direction of our saccades voluntarily but we cannot change their velocities. 0
Kandel; Principles of Neural Science 784 No time for visual feedback to modify the course of the saccade; corrections to the direction of movement are made in successive saccades. 0
Kandel; Principles of Neural Science 792 Saccades are controlled by the cerebral cortex. 8
Kandel; Principles of Neural Science 792 Eye movements are a component of the cognitive behavior of higher mammals. 0
Kandel; Principles of Neural Science 792 Cortex controls the saccadic system through the superior colliculus. 0
Kandel; Principles of Neural Science 792 Superior colliculus is a major visuomotor integrator region. 0
Kandel; Principles of Neural Science 793 Superior colliculus is controlled by two regions of the cerebral cortex. Brodmann's area 7 of the posterior parietal cortex modulates visual attention, and the frontal eye field of Brodmann's area 8 provides motor commands. 1
Kandel; Principles of Neural Science 794 Parietal cortex controls visual attention. 1
Kandel; Principles of Neural Science 801 Vestibular system 7
Kandel; Principles of Neural Science 816 Posture 15
Kandel; Principles of Neural Science 832 Cerebellum 16
Kandel; Principles of Neural Science 832 Cerebellum constitutes only 10% of the total volume of the brain but contains more than half of its neurons. 0
Kandel; Principles of Neural Science 832 Cerebellum neurons are arranged in a highly regular manner as repeating units, each of which is a basic circuit module. 0
Kandel; Principles of Neural Science 832 Cerebellum is divided into several distinct regions, each of which receives projections from different portions of the brain and spinal cord and projects to different motor systems. 0
Kandel; Principles of Neural Science 832 Regions of the cerebellum performed similar computational operations but on different inputs. 0
Kandel; Principles of Neural Science 832 Cerebellum influences the motor systems by evaluating disparities between intention and action. 0
Kandel; Principles of Neural Science 832 Cerebellum adjusts the operation of motor centers in the cortex and brain stem while a movement is in progress as well as during repetitions of the same movement. 0
Kandel; Principles of Neural Science 832 Cerebellum is provided with extensive information about the goals, commands, and feedback signals associated with the programming and execution of movement. 0
Kandel; Principles of Neural Science 832 40 times more axons project into the cerebellum than exit from it. 0
Kandel; Principles of Neural Science 832 Output projections of the cerebellum are focused mainly on the premotor and motor systems of the cerebral cortex and brain stem, systems that control spinal interneurons and motor neurons directly. 0
Kandel; Principles of Neural Science 832 Synaptic transmission in the cerebellum's circuit modules can be modified, a feature crucial for a motor adaptation and learning. 0
Kandel; Principles of Neural Science 833 Cerebellum is not necessary for basic elements of perception or movement. 1
Kandel; Principles of Neural Science 833 Damage to the cerebellum disrupts the spatial accuracy and temporal coordination of movement.  It also markedly impairs motor learning and certain cognitive functions. 0
Kandel; Principles of Neural Science 833 Cerebellum is connected to the dorsal aspect of the brain stem by three symmetrical pairs of tracks: (1) inferior cerebellar peduncle, (2) middle cerebellar peduncle, (3) superior cerebellar peduncle. 0
Kandel; Principles of Neural Science 833 Superior cerebellar peduncle contains most of the afferent projections. 0
Kandel; Principles of Neural Science 835 Cerebellar cortex has a simple three layered structure consisting of only five types of neurons. 2
Kandel; Principles of Neural Science 835 Purkinje neurons have large cell bodies (50-80 µ) and fanlike dendritic organization that extends upward into the molecular layer. 0
Kandel; Principles of Neural Science 835 Purkinje neurons provide the output of the cerebellar cortex which is entirely inhibitory and mediated by the neurotransmitter GABA. 0
Kandel; Principles of Neural Science 835 Innermost or granular layer of the cerebellar cortex contains a vast number (estimated at 1011)  granule cells. 0
Kandel; Principles of Neural Science 835 Cerebellum received two main types of afferent inputs, mossy fibers and climbing fibers. 0
Kandel; Principles of Neural Science 837 Mossy fibers originate from nuclei and the spinal cord and brain stem. 2
Kandel; Principles of Neural Science 837 In humans each Purkinje cell receives input from as many as one million granule cells, each of which collects input from many mossy fibers. 0
Kandel; Principles of Neural Science 837 Climbing fibers originate from the inferior olivary nucleus and convey somatosensory, visual, or cerebral cortical information. 0
Kandel; Principles of Neural Science 837 Climbing fibers are so named because they wrap around the cell bodies and proximal dendrites of Purkinje neurons like vines on a tree, making numerous synaptic contacts. 0
Kandel; Principles of Neural Science 837 Individual Purkinje neurons receive synaptic input from only a single climbing fiber, whereas each climbing fiber contacts 1-10 Purkinje neurons. 0
Kandel; Principles of Neural Science 837 Terminals of the climbing fibers in the cerebellar cortex are arranged topographically. 0
Kandel; Principles of Neural Science 837 Highly specific connectivity of the climbing fiber system contrasts markedly with the massive convergence and divergence of the mossy and parallel fibers. 0
Kandel; Principles of Neural Science 837 Climbing fibers have unusually powerful synaptic effects on Purkinje neurons. 0
Kandel; Principles of Neural Science 846 Cerebrocerebellum has a role in the planning and programming of hand movements. 9
Kandel; Principles of Neural Science 846 Cerebellum has cognitive functions independent of motor functions. 0
Kandel; Principles of Neural Science 847 Inferior olive, the source of climbing fibers to the cerebellar cortex. 1
Kandel; Principles of Neural Science 849 The kind of motor adaptation and learning with which the cerebellum is concerned requires trial-and-error practice.  Once the behavior becomes adapted as learned, it is performed automatically. 2
Kandel; Principles of Neural Science 849 After a knee jerk produced by the tap of a reflex hammer, the leg normally comes to rest after the jerk.  In patients who have cerebellar disease, the leg may oscillate up to 6 or 8 times before coming to rest. 0
Kandel; Principles of Neural Science 850 Cerebellum compares internal feedback signals that report intended movement with external feedback signals that report actual movement. When movement is repeated, the cerebellum is able to generate corrective signals and gradually reduce the error. 1
Kandel; Principles of Neural Science 850 Corrective signals generated by the cerebellum are feed-forward or anticipatory actions that operate on the descending motor systems of the brain stem and cerebral cortex. 0
Kandel; Principles of Neural Science 850 Oscillations and tremor that follow lesions of the cerebellum are due to the failure of feed-forward mechanisms. 0
Kandel; Principles of Neural Science 850 Cerebellum also plays a role in motor learning.  Climbing fibers might participate in motor learning.  Because of their low firing frequencies, climbing fibers have a very modest capability for transmitting moment-to-moment changes in sensory information.  Instead, they are thought to be involved in detecting the error in one movement and in changing the program for the next movement. 0
Kandel; Principles of Neural Science 850 Cerebellum seems to have a role in some purely mental operations.  Cerebellum's cognitive functions appear to be similar to its motor functions. 0
Kandel; Principles of Neural Science 850 Lateral cerebellum appears to be particularly important for learning both motor and cognitive tasks in which skilled responses are developed through repeated practice. 0
Kandel; Principles of Neural Science 853 Basal Ganglia 3
Kandel; Principles of Neural Science 853 Basal ganglia do not have direct input or output connections with the spinal cord. 0
Kandel; Principles of Neural Science 853 Basal ganglia receive their primary input from the cerebral cortex and send their output to the brain stem and, via the thalamus, back to the prefrontal, premoter, and motor cortices. 0
Kandel; Principles of Neural Science 853 Motor functions of the basal ganglia are mediated, in large part, by the motor areas of the frontal cortex. 0
Kandel; Principles of Neural Science 854 Motor actions of the basal ganglia are mediated in large part through the supplementary, premotor, and motor cortices via the pyramidal system. 1
Kandel; Principles of Neural Science 854 Basal ganglia consists of several interconnected subcortical nuclei with major projections to the cerebral cortex, thalamus,  and certain brain stem nuclei. 0
Kandel; Principles of Neural Science 854 Basal ganglia receive major inputs from the cerebral cortex and thalamus and send their outputs back to the cortex (via the thalamus) and to the brain stem. 0
Kandel; Principles of Neural Science 854 Basal ganglia are major components of large cortical-subcortical reentrant circuits linking cortex and thalamus. 0
Kandel; Principles of Neural Science 855 Four principal nuclei of the basal ganglia are: (1) striatum, (2) globus pallidus, (3) substantia nigra (consisting of pars reticulata and pars compacta), and (4) subthalamic nucleus. 1
Kandel; Principles of Neural Science 855 Striatum consists of three subdivisions: (1) caudate nucleus, (2) putamen, and (3) ventral striatum (which includes the nucleus accumbens). 0
Kandel; Principles of Neural Science 855 Internal capsule -- a major collection of fibers that runs between the neocortex and the thalamus in both directions. 0
Kandel; Principles of Neural Science 855 Striatum is the major recipient of inputs to the basal ganglia from the cerebral cortex, thalamus, and brain stem. 0
Kandel; Principles of Neural Science 855 Striatum neurons project to the globus pallidus and substantia nigra. 0
Kandel; Principles of Neural Science 855 Globus pallidus and substantia nigra give rise to the major output projections from the basal ganglia. 0
Kandel; Principles of Neural Science 855 Globus pallidus lies medial to the putamen, just lateral to the internal capsule, and is divided into external and internal segments. 0
Kandel; Principles of Neural Science 855 Cells of the substantia nigra pars compacta are dopaminergic and contain neuromelanin, a dark pigment. 0
Kandel; Principles of Neural Science 855 Subthalamic nucleus cells (glutamatergic) are the only excitatory projections of the basal ganglia. 0
Kandel; Principles of Neural Science 856 Striatum also receives excitatory inputs from the intralamina nuclei of the thalamus, dopaminergic projections from the midbrain, and serotonergic input from the raphe nuclei. 1
Kandel; Principles of Neural Science 856 Although the striatum appears homogeneous, it is anatomically and functionally highly heterogeneous. 0
Kandel; Principles of Neural Science 856 Although the striatum contains several distinct cell types, 95% of them are GABA-ergic medium spiny projection neurons. 0
Kandel; Principles of Neural Science 856 Medium spiny projection neurons of the striatum are both major targets of cortical input and the sole source of output. 0
Kandel; Principles of Neural Science 856 Medium spiny projection neurons of the striatum are largely quiescent except during movement or in response to peripheral stimuli. 0
Kandel; Principles of Neural Science 856 The two output nuclei of the basal ganglia, the internal pallidal segment and the substantia nigra pars reticular, tonically inhibit their target nuclei in the thalamus and brain stem. 0
Kandel; Principles of Neural Science 856 Inhibitory output of the basal ganglia is modulated by two parallel pathways that run from the striatum to the two output nuclei:  one direct and the other indirect. 0
Kandel; Principles of Neural Science 856 Indirect pathway passes first to the external pallidal segment (GPe), then to the subthalamic nucleus (SN), and finally to the output nuclei of the internal pallidal segment (GPi). 0
Kandel; Principles of Neural Science 857 Projection from the subthalamic nucleus is the only excitatory intrinsic connection of the basal ganglia; all others GABA-ergic and inhibitory. 1
Kandel; Principles of Neural Science 857 Neurons in the two output nuclei of the basal ganglia discharge tonically at high frequency. 0
Kandel; Principles of Neural Science 857 When excitatory inputs transiently activate the direct pathway from the striatum to the pallidum, tonically active neurons in the pallidum are briefly suppressed, permitting the thalamus and ultimately the cortex to be activated. 0
Kandel; Principles of Neural Science 857 Activation of the direct pathway disinhibits the thalamus, thereby increasing thalamocortical activity. 0
Kandel; Principles of Neural Science 857 Activation of the indirect pathway further inhibits thalamocortical neurons. 0
Kandel; Principles of Neural Science 857 Activation of the direct pathway facilitates movement, whereas activation of the indirect pathway inhibits movement. 0
Kandel; Principles of Neural Science 857 Dopaminergic inputs to the two pathways lead to the same effect -- reducing inhibition of the thalamocortical neurons and thus facilitating movements initiated in the cortex. 0
Kandel; Principles of Neural Science 857 Without dopaminergic action in the striatum, activity of the output nuclei increases.  This increased output in turn increases inhibition of the thalamocortical neurons that otherwise facilitate initiation of movement. 0
Kandel; Principles of Neural Science 857 Basal ganglia also contribute to a variety of behaviors other than voluntary movement. 0
Kandel; Principles of Neural Science 857 Basal ganglia have extensive and highly organized connections with virtually the entire cerebral cortex, as well as the hippocampus and amygdala. 0
Kandel; Principles of Neural Science 858 Each area of the neocortex projects to a discrete region of the striatum and does so in a highly topographic manner. 1
Kandel; Principles of Neural Science 858 Association areas project to the caudate and rostral putamen. 0
Kandel; Principles of Neural Science 858 Sensorimotor areas project to most of the central and caudal putamen. 0
Kandel; Principles of Neural Science 858 Limbic areas project to the ventral striatum and olfactory tubercle. 0
Kandel; Principles of Neural Science 858 Segregated basal ganglia--thalamocortical circuits. 0
Kandel; Principles of Neural Science 858 Structural convergence and functional integration occur within, rather than between, the five identified basal ganglia--thalamocortical circuits. 0
Kandel; Principles of Neural Science 858 Given the highly topographic connections between the striatum and the pallidum and between the pallidum and the subthalamic nucleus, it is unlikely that there is significant convergence between neighboring circuits. 0
Kandel; Principles of Neural Science 865 Glutamate is the principal excitatory transmitter in the central nervous system.  It is present in nerve terminals at high concentration (10-3 M). 7
Kandel; Principles of Neural Science 871 Brain stem -- small region of the central nervous system located between the spinal cord and the diencephalon. 6
Kandel; Principles of Neural Science 871 Brain stem contains the locus ceruleus, crucial for attention and for cognitive functions.  Fully half of all noradrenergic neurons of the brain are clustered together in this small nucleus. 0
Kandel; Principles of Neural Science 872 Hypothalamus, with closely linked structures in the brain stem and limbic system, acts directly on the internal environment through its control of the endocrine system and autonomic nervous system.  It acts indirectly through its control of emotional and motivational states. 1
Kandel; Principles of Neural Science 872 Hypothalamus, together with the brain stem below and the cerebral cortex above, maintain a general state of arousal, which ranges from excitement and vigilance to drowsiness and stupor. 0
Kandel; Principles of Neural Science 872 Six neural systems in the brain stem modulate sensory, motor, and arousal systems. 0
Kandel; Principles of Neural Science 872 Dopaminergic pathways that connect midbrain to the limbic system and cortex are involved in reinforcement of behavior and therefore contribute to motivational state. 0
Kandel; Principles of Neural Science 872 Addictive drugs such as nicotine, alcohol, opiates, and cocaine are thought to produce their actions by co-opting the same neural pathways that positively reinforce behaviors essential for survival. 0
Kandel; Principles of Neural Science 873 Brain Stem, Reflexive behavior, and the Cranial Nerves 1
Kandel; Principles of Neural Science 873 Basic behaviors are organized by the brain stem and consist of relatively simple stereotypic motor responses. 0
Kandel; Principles of Neural Science 873 Feeding involves coordination of chewing, licking, and swallowing, motor responses that are controlled by local ensembles of neurons in the brain stem. 0
Kandel; Principles of Neural Science 873 Many complex human responses are made up of relatively simple, stereotyped motor responses governed by the brain stem. 0
Kandel; Principles of Neural Science 873 Infants can cry, smile, suckle, and move their eyes, face, arms, and legs. 0
Kandel; Principles of Neural Science 873 Brain stem can organize virtually the entire repertory of newborn's behavior. 0
Kandel; Principles of Neural Science 873 The core of the brain stem is the reticular formation.  It is homologous to the intermediate gray matter of the spinal cord and is likewise complex. 0
Kandel; Principles of Neural Science 873 Like the spinal cord, the reticular formation of the brain stem contains ensembles of local circuit interneurons that generate motor patterns and coordinate reflexes and simple stereotyped behaviors. 0
Kandel; Principles of Neural Science 874 Functions of the cranial nerves (table) 1
Kandel; Principles of Neural Science 880 Intermediate gray matter of the spinal cord contains primarily interneurons that coordinate spinal reflexes and motor responses. 6
Kandel; Principles of Neural Science 885 Medulla includes the pyramidal tracts and the inferior olivary nuclei. 5
Kandel; Principles of Neural Science 885 Core of the brain stem tegmentum is called the reticular formation.  This region is homologous to the intermediate gray matter of the spinal cord, containing interneurons responsible for generating spinal reflexes and simple motor patterns. 0
Kandel; Principles of Neural Science 885 Viseral functions of the Vegas nerve. 0
Kandel; Principles of Neural Science 887 Simple motor responses can be assembled into more complex behaviors under voluntary control by the forebrain.  The precise patterns of motor response are organized locally in the brain stem reticular formation. 2
Kandel; Principles of Neural Science 889 Brain Stem modulation of Sensation, Movement, and Consciousness. 2
Kandel; Principles of Neural Science 889 Reticular interneurons and local projections mediate reflexes and simple stereotyped behaviors, such as chewing and swallowing. 0
Kandel; Principles of Neural Science 889 Reticular formation has long projection axons that ascend to the forebrain or descend to the spinal cord. 0
Kandel; Principles of Neural Science 889 Reticular formation is composed of systems of neurons with specific neurotransmitters and connections. 0
Kandel; Principles of Neural Science 890 Major modulatory systems of the brain. (1) noradrenergic, (2) adrenergic, (3) dopaminergic, (4) serotonergic, (5) cholinergic, (6) histaminergic. 1
Kandel; Principles of Neural Science 890 Noradrenergic and adrenergic neurons in the medulla and pons.  (diagram) 0
Kandel; Principles of Neural Science 891 Adrenergic cell groups (diagram) 1
Kandel; Principles of Neural Science 891 Locus ceruleus, which maintains vigilance and responsiveness to unexpected environmental stimuli, has extensive projections to the cerebral cortex and cerebellum, as well as the descending projections to the brain stem and spinal cord. 0
Kandel; Principles of Neural Science 891 Noradrenergic neurons in the pons (diagram) 0
Kandel; Principles of Neural Science 892 Dopaminergic neurons in the brain stem and hypothalamus (diagram) 1
Kandel; Principles of Neural Science 893 Serotonergic neurons along the midline of the brain stem (diagram) 1
Kandel; Principles of Neural Science 894 Cholinergic neurons in the upper pontine tegmentum and basal forebrain diffusely innervate much of the brain stem and forebrain.  (diagram) 1
Kandel; Principles of Neural Science 895 The largest collection of noradrenergic neurons is in the pons in the locus ceruleus. 1
Kandel; Principles of Neural Science 895 Histaminergic neurons in the brain are located in the hypothalamus.  (diagram) 0
Kandel; Principles of Neural Science 895 Five monoaminergic systems of neurons in the brain stem. 0
Kandel; Principles of Neural Science 895 Each of these six neuronal systems has extensive connections in most areas of the brain and each plays a major role in modulating sensory, motor, and arousal tone. 0
Kandel; Principles of Neural Science 896 Ascending projections from the brain stem modulate arousal and consciousness. 1
Kandel; Principles of Neural Science 897 Ascending arousal system divides into two major branches at the junction of the midbrain and diencephalon.  One branch enters the thalamus, where it activates and modulates nuclei with extensive diffuse cortical projections.  Other branch travels through the lateral hypothalamus area, joined by other cell groups, all of which diffusely innervate the cerebral cortex. 1
Kandel; Principles of Neural Science 897 Ascending arousal system diffusely innervates the cerebral cortex. 0
Kandel; Principles of Neural Science 897 EEG invented in the late 1920s by Hans Berger, a Swiss psychiatrist. 0
Kandel; Principles of Neural Science 897 Electrical activity in the cerebral cortex reflects the firing patterns in the thalamocortical system, a necessary component of maintaining a waking state. 0
Kandel; Principles of Neural Science 898 Rhythmic nature of thalamic activity. 1
Kandel; Principles of Neural Science 899 Either branch of the ascending arousal system -- the pathway to the thalamus or the pathway through the hypothalamus -- can impair consciousness. 1
Kandel; Principles of Neural Science 899 Acute transections rostral to the level of the inferior colliculus invariably result in coma. 0
Kandel; Principles of Neural Science 900 Ascending arousal system consist of axons of cell populations in the upper brain stem, hypothalamus, and basal forebrain (diagram) 1
Kandel; Principles of Neural Science 900 Main pathway in the brain stem or its branches in the thalamus or hypothalamus can cause loss of consciousness. 0
Kandel; Principles of Neural Science 900 Large pyramidal neurons in the hippocampal formation and cerebral cortex (particularly layers 3 and 5) are the cells most severely damaged by inadequate oxygenation (hypoxia) or insufficient blood flow (ischemia). 0
Kandel; Principles of Neural Science 900 After a period of one or two weeks of coma, patients enter a contentless wake-sleep cycle call a 'persistent vegetative state.' 0
Kandel; Principles of Neural Science 900 Persistent vegetative state must be distinguished from 'brain death,' in which all brain functions cease. 0
Kandel; Principles of Neural Science 900 Brain dead patients may have spinal level motor responses, which may include patterned activity such as withdrawal movements or even and rare instances sitting up or moving the arms. 0
Kandel; Principles of Neural Science 900 Brain dead patients have no purposeful movements of the limbs, face, or eyes; no brainstem reflex responses to sensory stimulation. 0
Kandel; Principles of Neural Science 900 Human brain stem is capable of organizing many stereotyped behaviors, ranging from eye movements orofacial responses, postural control, and even walking. 0
Kandel; Principles of Neural Science 900 Brain stem regulates the overall level of activity of the forebrain by controlling wake-sleep cycles and modulating the passage of sensory information, especially pain, to the cerebral cortex. 0
Kandel; Principles of Neural Science 900 Locked in syndrome -- injury to the lower brainstem; patients remain awake, but the intact forebrain is unable to interact with the external world. Exact opposite of patients in a persistent vegetative state. 0
Kandel; Principles of Neural Science 900 Persistent vegetative state -- extensive forebrain impairment as a result of hypoxia; patients appear to be awake but lack completely the content of consciousness. 0
Kandel; Principles of Neural Science 904 Pupilloconstrictor system -- balance between parasympathetic and sympathetic. (diagram) 4
Kandel; Principles of Neural Science 905 Pupillary dilation is regulated by a descending pathway from the hypothalamus.  (diagram) 1
Kandel; Principles of Neural Science 910 Seizures and Epilepsy 5
Kandel; Principles of Neural Science 911 Modern surgical treatment for epilepsy dates to the work of Wilder Penfield and Herbert Jasper in Montréal in the early 1950s. 1
Kandel; Principles of Neural Science 911 About 3% of all people living to the age of 80 will be diagnosed with epilepsy. 0
Kandel; Principles of Neural Science 911 Symptoms of epilepsy are dependent on the location and extent of brain tissue that is affected. 0
Kandel; Principles of Neural Science 911 Seisures can be classified clinically into two categories: (1) partial and (2) generalized. 0
Kandel; Principles of Neural Science 913 A partial seizure may began as localized jerking in the right hand and progress to movements of the entire right arm. 2
Kandel; Principles of Neural Science 913 Generalized seizures began without a preceding oral or focal seizure and involve both hemispheres from the onset. 0
Kandel; Principles of Neural Science 913 The most common generalized seizure is the tonic-clonic or grand mal, seizure.  These convulsive seizures began abruptly, often with a grunt or cry. 0
Kandel; Principles of Neural Science 913 During the tonic phase the patient may fall to the ground rigid with clenched jaw, lose bladder or bowel control, and become blue.  The tonic phase typically last 30 seconds before evolving into clonic jerking of the extremities lasting 1-2 min. 0
Kandel; Principles of Neural Science 913 Clinically, it can be difficult to distinguish a primary generalized tonic-clonic seizure from a secondarily generalized tonic-clonic seizure with a brief aura. 0
Kandel; Principles of Neural Science 913 Recurrent unprovoked seizures constitute the minimal criteria for the diagnosis of epilepsy. 0
Kandel; Principles of Neural Science 913 Neurons are excitable cells.  It is logical to assume that seizures result either directly or indirectly from a change in the excitability of single neurons or groups of neurons. 0
Kandel; Principles of Neural Science 916 Deep structures such as the hippocampus, thalamus, or brain stem do not contribute directly to the surface EEG. 3
Kandel; Principles of Neural Science 916 Surface EEG shows typical patterns of activity that can be correlated with various stages of sleep and wakefulness. 0
Kandel; Principles of Neural Science 916 Normal human EEG shows activity over a range of 1-30 Hz with amplitudes in the range of 20-100 μV. 0
Kandel; Principles of Neural Science 916 Alpha waves (8-13 Hz) of moderate amplitude are typical of relaxed wakefulness and are most prominent over parietal and occipital sites. 0
Kandel; Principles of Neural Science 916 Lower-amplitude beta activity (13-30 Hz) is more prominent in frontal areas and over other regions during intense mental activity. 0
Kandel; Principles of Neural Science 916 Alerting a relaxed person results in the desynchronization of the EEG, with a reduction in alpha activity and an increase in beta. 0
Kandel; Principles of Neural Science 916 Theta waves (4-7 Hz) and delta waves (0.5-4 Hz) are normal during drowsiness and earliest slow wave sleep. 0
Kandel; Principles of Neural Science 917 Defining feature of partial (and secondarily generalized) seisures is that the abnormal electrical activity originates from a seizure focus. 1
Kandel; Principles of Neural Science 919 Normal response of a typical cortical pyramidal neuron to excitatory input is an excitatory postsynaptic potential (EPSP) followed by an inhibitory postsynaptic potential (IPSP). 2
Kandel; Principles of Neural Science 919 Benzodiazepines (Valium) enhance GABA-mediated inhibition and are the standard emergency treatment for prolonged repetitive seizures. 0
Kandel; Principles of Neural Science 920 Primary motor and sensory cortex are organized into vertical columns that run from the pial surface to the underlying white matter. 1
Kandel; Principles of Neural Science 920 Major input to the sensory cortex comes from the thalamus and terminates in a layer 4, whereas the output cells are in layer 5. 0
Kandel; Principles of Neural Science 920 Thalamus and cortex are connected by a reciprocal thalamocortical pathways. 0
Kandel; Principles of Neural Science 920 Intracortical connections occur via short U fibers between adjacent sulci and via the corpus callosum, the major interhemispheric connection. 0
Kandel; Principles of Neural Science 920 Epileptic seizure -- once both hemispheres become involved, the patient generally loses consciousness.  Seizure spread usually occurs rapidly during a few seconds. 0
Kandel; Principles of Neural Science 922 Generalized epileptic seizures evolve from thalamocortical circuits. 2
Kandel; Principles of Neural Science 922 A generalized seizure shows simultaneous disruption of normal brain activity in both cerebral hemispheres from the onset. 0
Kandel; Principles of Neural Science 922 A partial seizure that rapidly generalizes can be difficult to distinguish from a primary generalized seizure. 0
Kandel; Principles of Neural Science 924 Intrinsic bursting of thalamic relay neurons -- Rodolfo Llinás. 2
Kandel; Principles of Neural Science 924 Circuitry of the thalamus seems ideally suited to the generation of primary generalized seizures. 0
Kandel; Principles of Neural Science 925 Pioneering studies of Wilder Penfield in Montreal led to the recognition that removal of the temporal lobe in certain patients with partial seizures of hippocampal origin could reduce or cure epilepsy. 1
Kandel; Principles of Neural Science 925 Precise location of the seizure focus is essential. 0
Kandel; Principles of Neural Science 925 In a primary generalized seizure, diffuse interconnections between the thalamus and cortex are the primary route of seizure propagation. 0
Kandel; Principles of Neural Science 930 A single seizure does not warrant a diagnosis of epilepsy.  Normal individuals can have a seizure under extenuating circumstances. 5
Kandel; Principles of Neural Science 930 Generalized seizures may be due in part to genetic predisposition. 0
Kandel; Principles of Neural Science 931 Genetic epilepsy syndromes in humans have complex rather than simple Mendelian inheritance patterns, suggesting the involvement of many genes rather than a single one. 1
Kandel; Principles of Neural Science 931 Cortical malformations in patients with epilepsy, suggesting that altered cortical development may be a common cause of epilepsy. 0
Kandel; Principles of Neural Science 931 Epilepsy often develops after a discrete cortical injury. 0
Kandel; Principles of Neural Science 931 Brain areas such as the hippocampus are more susceptible to the development of epilepsy. 0
Kandel; Principles of Neural Science 931 Chronic stimulation of hippocampal inputs to the dentate gyrus or CA1 leads to hyperexcitability and the loss of the affected neurons. 0
Kandel; Principles of Neural Science 931 Death of neurons is thought to result from over excitation by the release of large amounts of the excitatory neurotransmitter glutamate. 0
Kandel; Principles of Neural Science 931 Dentate gyrus provides the main entry point to the hippocampal formation from the neocortex. 0
Kandel; Principles of Neural Science 931 Dentate gyrus can be thought of as the 'gatekeeper' of excitability in the hippocampus. 0
Kandel; Principles of Neural Science 932 Hypothetical role of the dentate gyrus as the 'gatekeeper' for seizures involving the hippocampus (diagram) 1
Kandel; Principles of Neural Science 933 Gradual loss of GABA-ergic surround inhibition is critical to the early steps in the progression of partial seizures. 1
Kandel; Principles of Neural Science 933 Generalized seizures are thought to arise from activity in thalamocortical circuits. 0
Kandel; Principles of Neural Science 934 Epilepsy surgery for selected patients, particularly those with complex partial seizures of hippocampal onset. 1
Kandel; Principles of Neural Science 936 Sleep and Dreaming 2
Kandel; Principles of Neural Science 937 Circadian rhythms are endogenous; they require a pacemaker or internal clock.  One major internal clock in mammals is this suprachiasmatic nucleus in the anterior hypothalamus. 1
Kandel; Principles of Neural Science 937 Humans usually fall asleep by entering non-REM sleep. 0
Kandel; Principles of Neural Science 937 REM sleep is characterized by rapid eye movements and also by complete inhibition of skeletal muscle tone. 0
Kandel; Principles of Neural Science 937 Most dreams occurr during REM sleep. 0
Kandel; Principles of Neural Science 937 During non-REM sleep, neuronal activity is low and metabolic rate and brain temperature are at their lowest. 0
Kandel; Principles of Neural Science 937 Parasympathetic activity dominates during the non-REM phase of sleep. Muscle tone and reflexes are intact. 0
Kandel; Principles of Neural Science 937 Awake people have low-voltage EEG activity (10-30 μV and 10-25 Hz). 0
Kandel; Principles of Neural Science 937 As people relax they show sinusoidal (alpha) activity of about 20-40 μV and 10 Hz. 0
Kandel; Principles of Neural Science 939 Non-REM and REM phases alternate cyclically during sleep. 2
Kandel; Principles of Neural Science 939 After about 70-80 minutes of non-REM sleep, the sleeper enters the first REM phase of the night, which lasts about 5-10 minutes. 0
Kandel; Principles of Neural Science 939 In humans, the length of the cycle from the start of non-REM sleep to the end of the first REM phase is about 90-110 minutes. 0
Kandel; Principles of Neural Science 939 Cycle of non-REM and REM sleep is typically repeated four to six times a night. 0
Kandel; Principles of Neural Science 939 Midbrain reticular formation promotes the waking state. 0
Kandel; Principles of Neural Science 940 Non-REM sleep is regulated by interacting sleep-inducing and arousal mechanisms. 1
Kandel; Principles of Neural Science 940 Synchronized synaptic potentials are generated by the rhythmic firing of thalamic relay neurons that project of the cortex. 0
Kandel; Principles of Neural Science 940 Rhythmic firing of the thalamic relay neurons is a result of actions of GABA-ergic neurons in the nucleus reticularis, a nucleus that forms a shell around the thalamus. 0
Kandel; Principles of Neural Science 941 Major regions of the brain stem and forebrain involved in sleep control are shown in a sagittal section (diagram) 1
Kandel; Principles of Neural Science 941 An important component of the midbrain arousal system arises from the cholinergic neurons in the midbrain and the adjacent dorsal pons. 0
Kandel; Principles of Neural Science 941 In the absence of the rhythmic firing of the reticular neurons, thalamocortical relay cells fire only asynchronously, resulting in the low-voltage EEG characteristic of waking and REM sleep. 0
Kandel; Principles of Neural Science 944 All mammals sleep. 3
Kandel; Principles of Neural Science 944 Daily sleep ranges from about 4-5 hours in giraffes and elephants to 18 hours or more in bats, opossums, and giant armadillos. 0
Kandel; Principles of Neural Science 944 Like mammals, birds showed non-REM and REM sleep, but their sleep episodes are much shorter; REM episodes may last only several seconds. 0
Kandel; Principles of Neural Science 944 It is likely that sleep is functionally important because it has persisted throughout the evolution of mammals and birds. 0
Kandel; Principles of Neural Science 944 Metabolic rate during sleep is only 15% less than during quiet wakefulness. 0
Kandel; Principles of Neural Science 944 Small mammals tend to sleep the most. 0
Kandel; Principles of Neural Science 945 REM sleep is neither necessary nor sufficient for dreaming. 1
Kandel; Principles of Neural Science 946 No theory of sleep has succeeded in explaining the exact function of sleep. 1
Kandel; Principles of Neural Science 948 Disorders of Sleep and Wakefulness 2
Kandel; Principles of Neural Science 960 Autonomic Nervous System and the Hypothalamus. 12
Kandel; Principles of Neural Science 964 Sympathetic and parasympathetic divisions of the autonomic nervous system (diagram) 4
I is 971 Hypertension, Atenolol 7
Kandel; Principles of Neural Science 974 Pathways that distribute viseral sensory information to the brain (diagram) 3
Kandel; Principles of Neural Science 975 Pathways that control autonomic responses (diagram) 1
Kandel; Principles of Neural Science 976 Structure of the hypothalamus (diagram) 1
Kandel; Principles of Neural Science 977 Hypothalamus contains an array of specialized cell groups with different functional roles. 1
Kandel; Principles of Neural Science 977 Hypothalamus is very small, but it is packed with a complex array of cell groups and fiber pathways. 0
Kandel; Principles of Neural Science 977 The most anterior part of the hypothalamus, overlying the optic chiasm, includes the circadian pacemaker (suprachiasmatic nucleus). 0
Kandel; Principles of Neural Science 977 Major nuclei of the hypothalamus are located for the most part in the medial part. 0
Kandel; Principles of Neural Science 977 Hypothalamus controls the pituitary gland both directly and indirectly through hormone releasing neurons  (diagram) 0
Kandel; Principles of Neural Science 978 Hypothalamus controls the endocrine system directly. 1
Kandel; Principles of Neural Science 979 Direct and indirect control form the basis of modern understanding of hypothalamic control of endocrine activity. 1
Kandel; Principles of Neural Science 980 In addition to the small molecule neurotransmitters -- ACh and norepinephrine -- a wide variety of peptides is thought to be released by all autonomic neurons. 1
Kandel; Principles of Neural Science 982 Emotional states and Feelings 2
Kandel; Principles of Neural Science 982 Pleasure, elation, euphoria, ecstasy, sadness, despondency, depression, fear, anxiety, anger, hostility, and calm -- these and  other emotions. 0
Kandel; Principles of Neural Science 982 Emotional state has two components: (1) a characteristic physical sensation and (2) a conscious feeling. 0
Kandel; Principles of Neural Science 982 The term 'emotion' sometimes is used to refer only to the bodily state, and the term 'feeling' is used to refer to the conscious sensation. 0
Kandel; Principles of Neural Science 982 Many drugs that affect the mind -- ranging from addictive street drugs to therapeutic agents -- do so by acting on specific neural circuits concerned with emotional states and feelings. 0
Kandel; Principles of Neural Science 982 Conscious feeling is mediated by the cerebral cortex, in part by the cingulate cortex and by the frontal lobes. 0
Kandel; Principles of Neural Science 982 Emotional responses involve subcortical structures: the amygdala, the hypothalamus, and the brain stem. 0
Kandel; Principles of Neural Science 983 The peripheral component of emotion also communicates emotion to others. 1
Kandel; Principles of Neural Science 983 Human's social communication of emotions is mediated primarily by the muscles that control facial and postural expressions. 0
Kandel; Principles of Neural Science 984 The feeling state, the conscious experience of emotion, occurs after the cortex receives signals about changes in our physiological state. 1
Kandel; Principles of Neural Science 984 Hypothalamus and thalamus have a key role in mediating emotion, including regulating the peripheral signs of emotion, and providing the cortex with the information required for the cognitive processing of emotion. 0
Kandel; Principles of Neural Science 985 During the past decade, the neural pathways for peripheral (autonomic) and central (evaluative) components of emotion have been identified with some precision. 1
Kandel; Principles of Neural Science 986 Peripheral component of emotion involves the hypothalamus, while the central, evaluative component, both unconscious and conscious, involves the cerebral cortex, especially the cingulate and prefrontal cortex. 1
Kandel; Principles of Neural Science 986 Amygdala coordinates the conscious experience of emotion and the peripheral expressions of emotion, in particular fear. 0
Kandel; Principles of Neural Science 986 Unconscious evaluation of the emotional significance of a stimulus begins before the conscious processing of a stimulus. 0
Kandel; Principles of Neural Science 986 Hippocampus is the core of the medial temporal lobe system concerned with conscious memory. 0
Kandel; Principles of Neural Science 986 Damage to the hippocampus interferes with remembering the cognitive features of fear -- where the fear provoking stimulus was and in what context it occurred. 0
Kandel; Principles of Neural Science 986 Cognitive systems present us with choices of action -- whereas unconscious appraisal systems limit the options to a few adaptively important choices. 0
Kandel; Principles of Neural Science 986 Memory has two major forms: (1) a conscious (explicit) memory for facts and personal events and (2) an unconscious (implicit) memory for motor and sensory experience. 0
Kandel; Principles of Neural Science 986 Memory of emotional states (autonomic and somatic responses) involves implicit memory storage, whereas memory of feelings involves explicit memory storage. 0
Kandel; Principles of Neural Science 986 Hypothalamus acts on the autonomic nervous system by modulating visceral reflex circuitry that is basically organized at the level of the brainstem. 0
Kandel; Principles of Neural Science 986 Hypothalamus is not only a nucleus for the autonomic nervous system, it is also a coordinating center that integrates various inputs to ensure a well-organized, coherent, and appropriate set of autonomic and somatic responses. 0
Kandel; Principles of Neural Science 987 Limbic system consists of a limbic lobe and subcortical structures. (diagram) 1
Kandel; Principles of Neural Science 987 Medial forebrain bundle. (diagram)  Connects limbic system with old reptilian brain by way of a very large bidirectional pathway. (Johnston, 111)   0
Kandel; Principles of Neural Science 987 Rabies virus characteristically attacks the hippocampus -- patients show profound changes in emotional state, including bouts of terror and rage. 0
Kandel; Principles of Neural Science 987 Hypothalamus communicates reciprocally with areas of the cerebral cortex; information about the conscious and peripheral aspects of emotion affect each other. 0
Kandel; Principles of Neural Science 987 Hippocampal formation processes information from the cingulate gyrus and conveys it via the fornix to the mammillary bodies of the hypothalamus. 0
Kandel; Principles of Neural Science 987 Fornix -- fiber bundle that carries part of the outflow of the hippocampus. 0
Kandel; Principles of Neural Science 987 Hypothalamus provides information to the cingulate gyrus by a pathway from the mammillary bodies to the anterior thalamic nuclei and from there to the cingulate gyrus. 0
Kandel; Principles of Neural Science 988 Amygdala is the part of the limbic system most specifically involved with emotional experience. 1
Kandel; Principles of Neural Science 989 Inferotemporal cortex is involved in the explicit memory of facial identity. 1
Kandel; Principles of Neural Science 989 Amygdala is concerned with the implicit memory of the appropriate cues that signal emotions expressed by faces. 0
Kandel; Principles of Neural Science 989 Recognition of emotional expression in faces involves the amygdala. 0
Kandel; Principles of Neural Science 989 Response of the left amygdala increases with increasing fearfulness and decreases with increasing happiness. 0
Kandel; Principles of Neural Science 989 Appropriate responses to the sight of emotionally charged signals are coded by the inferior temporal cortex. 0
Kandel; Principles of Neural Science 989 Neurons in the inferior temporal cortex respond to facial features, including the direction of gaze. 0
Kandel; Principles of Neural Science 989 Since the amygdala receives input from the inferior temporal cortex and has strong connections to the autonomic nervous system, it can mediate emotional responses to complex visual stimuli. 0
Kandel; Principles of Neural Science 990 Recognition of facial expressions is essential for successful social behavior. 1
Kandel; Principles of Neural Science 990 Amygdala is a complex structure, consisting of about 10 distinct nuclei. 0
Kandel; Principles of Neural Science 990 Amygdala mediates both inborn and acquired emotional responses. 0
Kandel; Principles of Neural Science 990 Sensory information about sound is conveyed to the basolateral complex from two sources: (1) directly and rapidly from the auditory nucleus in the thalamus, and (2) indirectly and more slowly from the primary sensory areas of the cortex. 0
Kandel; Principles of Neural Science 991 For many types of emotions, particularly fear, information conveyed from the thalamus to the amygdala is especially important because it can initiate short-latency, primitive emotional responses that may be important in situations of immediate danger. 1
Kandel; Principles of Neural Science 991 Fear-potentiated startle 0
Kandel; Principles of Neural Science 992 Emotional memories are not stored in the amygdala directly but are stored in the cingulate and parahippocampal cortices, with which the amygdala is interconnected. 1
Kandel; Principles of Neural Science 998 Motivational and Addictive states 6
Kandel; Principles of Neural Science 998 Cognitive aspects of behavior -- what a person knows about the outside world. 0
Kandel; Principles of Neural Science 998 Motivation -- a catch-all term that refers to a variety of neuronal and physiological factors that initiate, sustain, and correct behavior. 0
Kandel; Principles of Neural Science 998 Behaviorists, who dominated the study of behavior in the first half of the 20th century, largely ignored internal factors in their attempt to explain behavior. 0
Kandel; Principles of Neural Science 998 With the rise of cognitive psychology, the behaviorist paradigm has receded, and motivation with all its complexity has become the subject of serious scientific study. 0
Kandel; Principles of Neural Science 998 Drive states are the outcome of homeostatic processes related to hunger, thirst, and temperature regulation. 0
Kandel; Principles of Neural Science 998 Motivational states may be broadly classified into two types: (1) elementary drive states such as hunger, thirst, and temperature, and (2) personal or social aspirations. 0
Kandel; Principles of Neural Science 999 Personal and social aspirations represent a complex interplay between physiological and social forces, and between conscious and unconscious mental processes. 1
Kandel; Principles of Neural Science 999 Activities that enhance immediate survival, such as eating or drinking. 0
Kandel; Principles of Neural Science 999 Activities that ensure long-term survival, such as sexual activity or caring for offspring, are pleasurable, and there is a great natural urge to repeat these behaviors. 0
Kandel; Principles of Neural Science 999 Drive states have general effects; they increase our general level of arousal. 0
Kandel; Principles of Neural Science 999 Drive states serves three functions: (1) they direct behavior toward or away from a specific goal; (2) they organize individual behaviors into a coherent, goal oriented sequence; and (3) they increase general alertness, energizing the individual to act. 0
Kandel; Principles of Neural Science 999 Drive states are simple motivational states that can be modeled as servo-control systems. 0
Kandel; Principles of Neural Science 999 Physiological control involves both inhibitory and excitatory effects. 0
Kandel; Principles of Neural Science 1000 Integrator and controlling elements for temperature regulation are located in the hypothalamus. 1
Kandel; Principles of Neural Science 1001 Hypothalamus also controls endocrine responses to temperature challenges. 1
Kandel; Principles of Neural Science 1006 Hypothalamus regulates water balance. 5
Kandel; Principles of Neural Science 1007 Circadian rhythm for virtually every homeostatic function. 1
Kandel; Principles of Neural Science 1007 Pleasure is a key factor in controlling the motivated behavior of humans. 0
Kandel; Principles of Neural Science 1008 Cocaine craving can be elicited by environmental cues reminiscent of cocaine usage. 1
Kandel; Principles of Neural Science 1009 Human brain has relatively few dopaminergic neurons, equally divided between the substantia nigra and the ventral tegmental area. 1
Kandel; Principles of Neural Science 1009 Dopaminergic neurons send their axons to the nucleus accumbens, the striatum, and the frontal cortex, three structures thought to be involved in motivation. 0
Kandel; Principles of Neural Science 1011 Brain reward circuitry and the rat (diagram) 2
Kandel; Principles of Neural Science 1012 Motivational states involve neural mechanisms that are widely distributed throughout the brain, but hypothalamic mechanisms play a particularly prominent role. 1
Kandel; Principles of Neural Science 1012 Hypothalamus through its control of hormonal release and the autonomic nervous system, is involved in the regulation of behavioral states such as stress and anxiety. 0
Kandel; Principles of Neural Science 1012 Neural systems that mediate reward and pleasure use a variety in neurotransmitters, but dopamine in particular has been implicated. 0
Kandel; Principles of Neural Science 1019 Induction and Patterning of the Nervous System 7
Kandel; Principles of Neural Science 1019 Cells of the neural plate acquire differentiated properties, giving rise both to immature neurons and to glial cells. 0
Kandel; Principles of Neural Science 1019 Immature neurons migrate from zones of cell proliferation to their final positions and extend axons toward their target cells. 0
Kandel; Principles of Neural Science 1019 Contacts between growing axons and target cells initiates the process of selective synapse formation, during which some synapse contacts are strengthened and others eliminated. 0
Kandel; Principles of Neural Science 1019 Electrical and chemical signals passed across synapses can control patterns of conductivity. 0
Kandel; Principles of Neural Science 1019 Great variety of neural cell types -- both neurons and glial cells. 0
Kandel; Principles of Neural Science 1019 Estimated to be many hundreds of different neuronal types, far more than in any other organ of the body. 0
Kandel; Principles of Neural Science 1020 Neural plate folds in stages to form the neural tube.(diagram) 1
Kandel; Principles of Neural Science 1021 Successive stages and the development of the neural tube (diagram) 1
Kandel; Principles of Neural Science 1021  Neural development mechanisms are conserved in different organisms.  Molecular basis of neural development in vertebrates derives from organisms such as the fruit fly Drosophila melanogaster and the nematode worm Caenorhabditis elegans. 0
Kandel; Principles of Neural Science 1021 Entire nervous system arises from the ectoderm. 0
Kandel; Principles of Neural Science 1022 Forebrain; telencephalon -- cerebral cortex, basal ganglia, hippocampal formation, amygdala, olfactory bulb 1
Kandel; Principles of Neural Science 1022 Forebrain; diencephalon -- thalamus, hypothalamus, subthalamus, epithalamus, retina, optic nerve is tracts 0
Kandel; Principles of Neural Science 1022 Inductive signals control cell differentiation. 0
Kandel; Principles of Neural Science 1023 Neural plate is induced by signals from adjacent mesoderm. 1
Kandel; Principles of Neural Science 1025 Sonic hedgehog and BMP signaling pattern the neural tube along the dorsoventral axis. 2
Kandel; Principles of Neural Science 1026 Sonic hedgehog signaling controls cell identity and pattern in the ventral neural tube. 1
Kandel; Principles of Neural Science 1027 Neurons involved in sensory input are located in the dorsal half of the spinal cord, whereas those involved in motor output are located in the ventral half. 1
Kandel; Principles of Neural Science 1027 Early differentiation of cell types in the ventral neural tube is controlled by signals from the mesoderm cells. 0
Kandel; Principles of Neural Science 1027 Cell differentiation in the dorsal half is controlled by signals from non-neuronal cells in the epidermal ectoderm. 0
Kandel; Principles of Neural Science 1027 Sonic hedgehog (SHH) exerts a powerful influence on the development of the central nervous system. 0
Kandel; Principles of Neural Science 1027 Signaling pathway is triggered by the interaction of sonic hedgehog protein with a heterodimeric receptor complex. 0
Kandel; Principles of Neural Science 1027 Transmembrane protein named smoothened generates an intracellular signal that regulates several protein kinases and activates a class of transcription factors. 0
Kandel; Principles of Neural Science 1027 Sonic hedgehog acts not only as an inducer but also as a morphogen, a type of inductive signal that can direct different cell fates at different concentration thresholds. 0
Kandel; Principles of Neural Science 1029 Disruption of different components of the sonic hedgehog signaling pathway results in a wide variety of human diseases. 2
Kandel; Principles of Neural Science 1029 Dorsal neural tube is patterned by bone morphogenetic proteins (BMPs) secreted from the epidermal ectoderm and roof plate. 0
Kandel; Principles of Neural Science 1041 Generation and Survival of Nerve Cells 12
Kandel; Principles of Neural Science 1063 Guidance of Axons to their Targets 22
Kandel; Principles of Neural Science 1063 Many neurons extend over great distances -- up to several meters in a giraffe -- bypassing billions of potential but inappropriate synaptic targets before terminating in the correct area and recognizing the appropriate targets. 0
Kandel; Principles of Neural Science 1063 The pathways along which axons grow provide a large number of diverse molecular cues to guide axons to their targets, and the axons possess exquisitely specific receptors to recognize and interpret these cues. 0
Kandel; Principles of Neural Science 1069 The first axons to reach their targets when the embryo is very small, sometimes called "pioneers," respond to molecular cues embedded in cells or the extracellular matrix along their way. 6
Kandel; Principles of Neural Science 1069 Axons that arise later in development, when distances are longer and obstacles are more numerous, can reach their targets by following the pioneer neurons. 0
Kandel; Principles of Neural Science 1070 Negative cues can repulse advancing axons, causing them to turn, or prevent them from entering the wrong territory. 1
Kandel; Principles of Neural Science 1070 Long-range cues and clues soluble molecules that could use some produces cells and can attract or repel axons from afar, albeit with somewhat less precision. 0
Kandel; Principles of Neural Science 1070 Growth cones guide the axons by transducing positive and negative cues into signals that regulate the cytoskeleton and thereby determine the course and rate of axon outgrowth. 0
Kandel; Principles of Neural Science 1072 Growth cones are stimulated to advanced, retract, or turn. Several motors involving actin, myosin, and membrane components power these reactions. 2
Kandel; Principles of Neural Science 1073 Particularly critical for axonal guidance is the coupling between the sensory and motor capabilities of the growth cone. 1
Kandel; Principles of Neural Science 1073 Second messengers affect the organization of the cytoskeleton, thereby regulating the direction and rate at which the growth cone moves. 0
Kandel; Principles of Neural Science 1074 Numerous effects of embryonic environment on the growing axon are mediated by hundreds of molecular species. 1
Kandel; Principles of Neural Science 1077 Cadherins are a group of at least 100 related membrane-spanning glycoproteins. 3
Kandel; Principles of Neural Science 1077 Cells throughout the body express cadherins. 0
Kandel; Principles of Neural Science 1077 Cadherins on adjoining membranes interact to form adhesive bonds. Each cadherins prefers to bind to its own kind, forming homophilic interactions. 0
Kandel; Principles of Neural Science 1078 Chemotaxis, in which the axon grows up or down a concentration gradient of a chemotropic factor and is thereby guided in a particular direction. This mechanism is called tropism. 1
Kandel; Principles of Neural Science 1081 Ephrins and semaphorins guide growth cones by providing inhibitory signals. 3
Kandel; Principles of Neural Science 1081 Axons are guided by long-range inhibitory as well as attractive cues, essentially negative chemotactic factors that axons grow away from. 0
Kandel; Principles of Neural Science 1081 Numerous guidance cues line the pathway that anyone axon follows; the growth cone can resolve multiple queues; and several large families of molecules are involved in the transmission and reception of guidance cues. 0
Kandel; Principles of Neural Science 1084 Axons receive guidance at intervals along the way. Some axons grow early in the embryo, when distances are short, serving as scaffolds for later growing axons. Other axons grow along epithelial surfaces or extracellular matrices. Sometimes so-called guidepost cells mark sites at which axons need to make divergent choices. 3
Kandel; Principles of Neural Science 1084 Growth cone is both a sensory and motive structure. It bears numerous receptors to which environmental cues bind as well as cytoskeletal proteins and actin-based motors that propel it forward. 0
Kandel; Principles of Neural Science 1087 Formation and Regeneration of Synapses 3
Kandel; Principles of Neural Science 1115 Sensory Experience and the Fine-Tuning of Synaptic Connections 28
Kandel; Principles of Neural Science 1117 "Critical period" in the maturation of the cortical connections that control visual perception. 2
Kandel; Principles of Neural Science 118 Inputs from the two eyes to the cortex    terminate in alternating ocular dominance columns    in the primary visual cortex. -999
Kandel; Principles of Neural Science 1131 Sexual Differentiation of the Nervous System 1013
Kandel; Principles of Neural Science 1131 In many mammalian species the brain is inherently feminine.  Masculine characteristics of structure and function are imposed on the developing central nervous system by the action of testicular hormones during a critical period. 0
Kandel; Principles of Neural Science 1136 Testosterone is often thought of as a male sex hormone and estrogen and progesterone as female sex hormones.  In reality, each sex has a particular balance of several hormones, although testosterone does predominate in males and estrogen or progesterone in females. 5
Kandel; Principles of Neural Science 1142 Men perform better than women on visuospatial tasks, and women perform better than men on verbal tasks. 6
Kandel; Principles of Neural Science 1142 Brain function in men appears to be more lateralized than in women. 0
Kandel; Principles of Neural Science 1142 Women are more likely than men to recover speech after a stroke that damages cortical speech areas. 0
Kandel; Principles of Neural Science 1143 There may be a genetic and anatomical basis for homosexuality. 1
Kandel; Principles of Neural Science 1145 Much recent research has focused on neural correlates of the homosexuality. 2
Kandel; Principles of Neural Science 1146 A complex behavioral trait such as sexual orientation is unlikely to be caused by a single gene, a single hormone-induced alteration in brain structure, or a single experience in life. 1
Kandel; Principles of Neural Science 1146 Etiology of homosexuality must be multifactorial. 0
Kandel; Principles of Neural Science 1146 Central nervous system appears to be an inherently feminine.  For the mammalian brain to have functional and structural characteristics typical of the male of the species, the developing brain must be exposed to testicular hormones. 0
Kandel; Principles of Neural Science 1146 Marked changes in central nervous system structure are likely to occur at puberty. 0
Kandel; Principles of Neural Science 1149 Aging of the Brain and Dementia of Alzheimer type 3
Kandel; Principles of Neural Science 1169 Language and the Aphasias 20
Kandel; Principles of Neural Science 1188 Disorders of Thought and Volition: Schizophrenia 19
Kandel; Principles of Neural Science 1209 Disorders of Mood: Depression, Mania, and Anxiety disorders 21
Kandel; Principles of Neural Science 1227 Learning and Memory 18
Kandel; Principles of Neural Science 1247 Cellular mechanisms of Learning and the Biological Basis of Individuality 20
Kandel; Principles of Neural Science 1247 Molecular mechanisms of memory storage are highly conserved throughout evolution. 0
Kandel; Principles of Neural Science 1248 Elementary forms of learning:   habituation, sensitization, and classical conditioning. 1
Kandel; Principles of Neural Science 1248 Vertebrate reflexes such as flexion reflexes, fear responses and eyeblink. 0
Kandel; Principles of Neural Science 1248 Habituation -- simplest form of implicit learning, an animal learns about the properties of novel stimuli that are harmless. 0
Kandel; Principles of Neural Science 1248 Charles Sherrington study of reflexes. 0
Kandel; Principles of Neural Science 1248 Organization of interneurons in the spinal cord for vertebrates is quite complex. 0
Kandel; Principles of Neural Science 1248 Marine sea slug Aplysia has a Central Nervous System containing only about 20,000 Central nerve cells, an excellent simple system for studying implicit forms of memory. 0
Kandel; Principles of Neural Science 1249 Synaptic depression of the connections made by sensory neurons, interneurons, or both is a common mechanism for hibituation. 1
Kandel; Principles of Neural Science 1250 Sensitization -- when an animal repeatedly encounters a harmful stimulus, it learns to respond more vigorously, even to similar harmless stimuli. 1
Kandel; Principles of Neural Science 1250 Sensitization is more complex than habituation 0
Kandel; Principles of Neural Science 1252 Classical conditioning is a more complex form of learning than sensitization.  Rather than learning only about one stimulus, the organism learns to associate one type of stimulus with another. 2
Kandel; Principles of Neural Science 1254 Long-term storage of implicit memory for sensitization and classical conditioning involves the cAMP-PKA-MAPK-CREB Pathway. 2
Kandel; Principles of Neural Science 1257 Hippocampus -- 3 major afferent pathways (diagram) 3
Kandel; Principles of Neural Science 1257 Perforant fiber pathway from the entorhinal cortex forms excitatory connections with the granule cells of the dentate gyrus. 0
Kandel; Principles of Neural Science 1257 Granule cells of the dentate gyrus have axons that form the mossy fiber pathway, which connects with the pyramidal cells in area CA3 of the hippocampus. 0
Kandel; Principles of Neural Science 1257 Pyramidal cells in CA3 project to the pyramidal cells in CA1 by means of the Shaffer collateral pathway. 0
Kandel; Principles of Neural Science 1257 LTP is nonassociative in the mossy fiber pathway and is associative in the perforant fiber pathway and Shaffer collateral pathway. 0
Kandel; Principles of Neural Science 1258 Long term potentiation (LTP) of the mossy fiber pathway of the CA3 region of the hippocampus. (diagram) 1
Kandel; Principles of Neural Science 1259 Long-term potentiation (LTP) in the Shaffer collateral pathway to the CA1 region of the hippocampus. (diagram) 1
Kandel; Principles of Neural Science 1260 LTP in the Shaffer collateral pathway requires simultaneous firing in both the postsynaptic and presynaptic neurons. 1
Kandel; Principles of Neural Science 1260 Hebb's rule, proposed in 1949. 0
Kandel; Principles of Neural Science 1260 Fine-tuning synaptic connections during the late stages of development. 0
Kandel; Principles of Neural Science 1260 Induction of LTP in the CA1 region of the hippocampus depends on four postsynaptic factors: (1) postsynaptic depolarization, (2) activation of NMDA receptors, (3) influx of Ca2+, and (4) activation by Ca2+ of several second messenger systems in the postsynaptic cell. 0
Kandel; Principles of Neural Science 1262 Since induction of LTP requires events only in the postsynaptic cell (Ca2+ influx through the NMDA channels), whereas the expression of LTP is due in part to subsequent events in the presynaptic cells (increase in transmitter release), the presynaptic cells must somehow receive information that LTP has been induced. 2
Kandel; Principles of Neural Science 1262 Nitric oxide (NO), a gas that diffuses readily from cell to cell, may be a retrograde messenger from postsynaptic cell to presynaptic cell, involved in LTP. 0
Kandel; Principles of Neural Science 1262 Shaffer collateral pathways.  LTP in CA1 users two associative mechanisms in series: (1) a Hebbian mechanism (simultaneous firing in both the pre- and postsynaptic cells), and (2) activity-dependent presynaptic facilitation. 0
Kandel; Principles of Neural Science 1262 A similar set of mechanisms is responsible for LTP in the perforant pathway. 0
Kandel; Principles of Neural Science 1262 LTP has phases.  Early LTP lasts 1-3 hours; does not require protein synthesis. 0
Kandel; Principles of Neural Science 1262 Four or more trains induce a more persistent phase of the LTP (called late LTP) that lasts for at least 24 hours and requires new protein and RNA synthesis. 0
Kandel; Principles of Neural Science 1262 Late phase LTD requires the synthesis of new mRNA and protein and recruits the cAMP-PKA-MAPK-CREB signaling pathway. 0
Kandel; Principles of Neural Science 1264 Late phase LTP involves the activation, perhaps the growth, of additional presynaptic machinery for transmitter release and the insertion of new clusters of postsynaptic receptors. 2
Kandel; Principles of Neural Science 1264 Hippocampus contains a cognitive map of the spatial environment in which an animal moves. 0
Kandel; Principles of Neural Science 1264 Location of an animal in a particular space is encoded in the firing pattern of individual pyramidal cells. 0
Kandel; Principles of Neural Science 1264 Mouse's hippocampus has about a million pyramidal cells, each of which is potentially a place cell. 0
Kandel; Principles of Neural Science 1264 Mouse's whereabouts are signaled by the discharge of a unique population of hippocampal place cells. 0
Kandel; Principles of Neural Science 1264 Animal is thought to form a "place field," an internal representation of the space that it occupies. 0
Kandel; Principles of Neural Science 1264 When an animal enters a new environment, new place fields are formed within minutes and are stable for weeks to months. 0
Kandel; Principles of Neural Science 1266 Same pyramidal cells may signal different information in different environments and can be used in more than one spatial map. 2
Kandel; Principles of Neural Science 1266 Low frequencies of stimulation, in the range of 1-10 Hz, are in the physiological range of a prominent spontaneous rhythm in the hippocampus, called the theta rhythm. 0
Kandel; Principles of Neural Science 1266 Rapid formation of place fields, and their persistence for weeks. 0
Kandel; Principles of Neural Science 1274 cAMP-dependent protein kinase, MAP kinase, and CREB, to convert labile short-term memory into long-term memory. 8
Kandel; Principles of Neural Science 1274 Learning can lead to structural alterations in the brain. 0
Kandel; Principles of Neural Science 1274 Brains of identical twins are uniquely modified by experience. 0
Kandel; Principles of Neural Science 1275 Distinctive modifications of brain architecture, along with unique genetic makeup, constitute a biological basis for individuality. 1
Kandel; Principles of Neural Science 1275 Practice may strengthen the effectiveness of existing patterns of connections. 0
Kandel; Principles of Neural Science 1275 Basis of contemporary neural science is that all mental processes are biological. 0
Kandel; Principles of Neural Science 1277 Ongoing modification of synapses throughout life means that all behavior of an individual is produced by genetic and developmental mechanisms acting on the brain. 2
Kandel; Principles of Neural Science 1277 Brain stores an internal representation of the world. 0
Kandel; Principles of Neural Science 1280 Current flow in Neurons 3
Kandel; Principles of Neural Science 1288 Ventricular organization of Cerebrospinal Fluid: Blood-Brain Barrier, Brain Edema, and Hydrocephalus  8
Kandel; Principles of Neural Science 1302 Circulation of the Brain 14
Kandel; Principles of Neural Science 1317 Consciousness and the Neurobiology of the 21st-century 15