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Comprehensive set of vocabulary flashcards covering neural structure, communication, neuropharmacology, development, somatosensation, audition, vestibular and chemical senses, and vision.
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Dendrites
Branch-like extensions that receive incoming signals from other neurons.
Cell body (soma)
Contains the nucleus; integrates incoming signals and maintains the cell.
Axon
Long fiber that carries the action potential away from the cell body.
Axon terminals
Axon endings that release neurotransmitter into the synapse.
Information flow through a neuron and synapse
Dendrites receive, soma integrates, action potential travels down axon, terminals release neurotransmitter across the cleft onto postsynaptic receptors.
Glial cells
Support cells: astrocytes (nutrients, blood-brain barrier, cleanup), oligodendrocytes (CNS myelin), Schwann cells (PNS myelin), microglia (immune defense).
Central nervous system (CNS)
The brain and spinal cord.
Peripheral nervous system (PNS)
All nerves outside the brain and spinal cord; links the CNS to body and environment.
Somatic nervous system
PNS division carrying sensory input and controlling voluntary skeletal muscles.
Autonomic nervous system
PNS division controlling involuntary functions of organs and glands.
Sympathetic vs. parasympathetic
Sympathetic: fight-or-flight arousal (heart rate up). Parasympathetic: rest-and-digest conservation (heart rate down, digestion up).
Frontal lobe
Planning, decision making, voluntary movement (motor cortex), personality, speech production.
Parietal lobe
Touch and body sensation (somatosensory cortex), spatial processing, attention.
Temporal lobe
Hearing, language comprehension, object recognition, memory.
Occipital lobe
Primary visual processing.
Basal ganglia
Subcortical structures for initiating and smoothing voluntary movement and habits; damaged in Parkinson's and Huntington's.
Limbic system
Network for emotion, motivation, and memory (includes hippocampus and amygdala).
Hippocampus
Forms new long-term memories and supports spatial memory.
Amygdala
Processes fear and emotional significance; emotional memory.
Cerebellum
Coordinates movement, balance, timing, and motor learning.
Brainstem
Midbrain, pons, medulla; controls breathing, heart rate, arousal, and basic reflexes.
Resting membrane potential
About −70mV charge difference across the membrane (inside negative) when the neuron is not firing; set up by ion gradients, permeability, and the pump.
Diffusion
Movement of ions from high to low concentration.
Electrostatic pressure
Attraction of opposite charges and repulsion of like charges; pulls K+ back in and pushes Na+ in.
Selective permeability
Membrane lets some ions through more easily than others (more K+ leak channels than Na+), helping maintain the resting potential.
Sodium-potassium pump
Uses ATP to move 3Na+ out and 2K+ in, maintaining the gradients.
Action potential sequence
Threshold reached, Na+ channels open and Na+ rushes in (depolarization), Na+ channels inactivate, K+ channels open and K+ exits (repolarization), brief hyperpolarization, return to rest.
Threshold
Critical level of depolarization (about −55mV) that triggers an action potential.
All-or-none property
An action potential either fires at full size or not at all; stimulus intensity is coded by firing rate.
Depolarization
Membrane potential becomes less negative (toward or above 0), caused by Na+ influx.
Repolarization
Membrane returns toward resting potential as K+ flows out.
Hyperpolarization
Membrane becomes more negative than rest, making firing less likely; follows K+ overshoot.
Absolute refractory period
Time when Na+ channels are inactivated and no second action potential can fire; limits firing rate and keeps the signal moving one way.
Relative refractory period
Time right after when a stronger-than-normal stimulus can trigger an action potential, due to hyperpolarization.
Myelination
Fatty insulation that speeds conduction because the current jumps between gaps instead of traveling continuously.
Saltatory conduction
Action potential jumping from node to node along a myelinated axon.
Nodes of Ranvier
Gaps in the myelin where ion channels are concentrated and the action potential is regenerated.
Synaptic transmission steps
Action potential arrives, Ca2+ enters, vesicles release neurotransmitter, it binds postsynaptic receptors, then is cleared by reuptake, enzymes, or diffusion.
EPSP
Excitatory postsynaptic potential: small depolarization that moves the neuron toward threshold.
IPSP
Inhibitory postsynaptic potential: small hyperpolarization that moves the neuron away from threshold.
Spatial summation
EPSPs and IPSPs from different synapses at the same time add together.
Temporal summation
Rapid successive inputs at the same synapse add together.
Neural integration
Neuron sums all EPSPs and IPSPs; if the total reaches threshold at the axon hillock, it fires.
Criteria for a neurotransmitter
Made in the neuron, stored in the terminals, released with activity, causes a postsynaptic effect, mimicked by applying it, and has a removal mechanism.
Acetylcholine
Muscle contraction, attention, and memory; loss linked to Alzheimer's.
Dopamine
Movement (Parkinson's), reward and motivation; excess linked to psychosis.
Serotonin
Mood, sleep, and appetite; target of many antidepressants.
Norepinephrine
Arousal, alertness, and the stress response.
Glutamate
Main excitatory neurotransmitter; important in learning and memory.
GABA
Main inhibitory neurotransmitter.
Ionotropic receptors
Receptor is itself an ion channel; fast, brief effects.
Metabotropic receptors
Act through G proteins and second messengers; slower, longer lasting effects.
Agonist
Drug that mimics or enhances a neurotransmitter's effect.
Antagonist
Drug that blocks or reduces a neurotransmitter's effect.
Partial agonist
Binds a receptor but produces a weaker response than the full agonist.
Dose-response relationship
Higher doses produce greater effects, up to a maximum; shown as a curve.
Tolerance
Reduced drug effect with repeated use; involves receptor changes, faster metabolism, and compensatory (often conditioned) responses.
Drugs and neurotransmitter release
Drugs can increase or block release of a neurotransmitter from the terminals.
Drugs and reuptake
Drugs can block reuptake, leaving more neurotransmitter in the synapse.
Drugs and receptors
Drugs can activate or block receptors (agonists and antagonists).
Alcohol
Enhances GABA and inhibits glutamate; sedative depressant.
Cannabis
THC activates cannabinoid (CB1) receptors, mimicking endocannabinoids.
Nicotine
Agonist at nicotinic acetylcholine receptors; increases dopamine.
Opioids
Activate opioid receptors, mimicking endorphins; pain relief, euphoria, respiratory depression.
Stimulants
Boost dopamine and norepinephrine: cocaine blocks reuptake; amphetamine increases release and blocks reuptake.
Theories of addiction
Positive reinforcement (seeking pleasure), negative reinforcement (avoiding withdrawal), incentive-sensitization (cue "wanting" grows beyond "liking").
Ventral tegmental area (VTA)
Midbrain source of dopamine neurons in the reward pathway.
Nucleus accumbens
Forebrain target of VTA dopamine; key for reward and reinforcement.
Dopamine reward pathway
VTA to nucleus accumbens (mesolimbic path); activated by natural rewards and addictive drugs.
Neurogenesis
Birth of new neurons from stem cells.
Cell migration
Neurons travel to their final locations, guided by radial glia and chemical signals.
Differentiation
Cells become specific neuron types with specialized features.
Synaptogenesis
Axons grow to targets and form synapses.
Cell death
Many neurons (often about half) die during development.
Synapse rearrangement
Connections are refined and pruned based on activity and experience.
Neurotrophic factors
Chemicals (such as NGF, BDNF) that support neuron survival, growth, and connections.
Programmed cell death
Natural elimination of excess or poorly connected neurons; matches neuron numbers to targets and sharpens circuits.
Synaptic pruning
Removal of unused synapses; more synapses is not always better since pruning makes circuits efficient.
Sensitive periods
Time windows when experience has an especially strong effect on development.
Visual deprivation
Blocking input from one eye during a sensitive period weakens its cortical representation (amblyopia).
Genotype
An organism's genetic makeup.
Phenotype
Observable traits resulting from genotype plus environment.
Experience and gene expression
Experience can switch genes on or off without changing the DNA sequence.
Epigenetics
Study of changes in gene expression that do not alter the DNA sequence.
Methylation
Methyl groups attach to DNA, typically silencing the gene.
Gene-environment interaction
Genes set possibilities; environment and experience shape which are expressed.
Sensory transduction
Conversion of a physical stimulus into an electrical neural signal.
Labeled lines
Which neurons are activated tells the brain the type and location of the stimulus.
Pacinian corpuscles
Deep pressure and high-frequency vibration.
Meissner corpuscles
Light touch and low-frequency flutter; rapidly adapting, in fingertips.
Merkel discs
Sustained pressure, fine detail, edges, and texture.
Ruffini endings
Skin stretch and sustained pressure.
Receptive field
Area of the body (or visual field) where a stimulus changes a neuron's firing.
Phasic receptors
Respond at stimulus onset or change, then adapt quickly.
Tonic receptors
Keep firing during a sustained stimulus.
Sensory adaptation
Reduced response to a constant stimulus over time.
Touch pathway
Receptor, dorsal root, dorsal column up the spinal cord, crosses in medulla, thalamus, somatosensory cortex (parietal lobe).
Pain pathways
Spinothalamic route: fast A-delta fibers (sharp pain) and slow C fibers (dull, burning pain); crosses in the spinal cord, then thalamus and cortex.
Nociceptors
Receptors that detect damaging or potentially damaging stimuli.
Substance P
Neurotransmitter that transmits pain signals.