Anatomy and Physiology of Cells of the NS Flashcards

(46 cards)

1
Q

Soma

A

-Cell body of neuron
-Contains nucleus and most other organelles
-Common site of synaptic input (afferent)
-Contain receptors for neurotransmitters (subsynaptic membrane)

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2
Q

Dendrites

A

-Extension of the soma
-Common site of synaptic input (afferent)
-Contain receptors for neurotransmitters (subsynaptic membrane)

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3
Q

Axon hillock

A

-Anatomical transition from soma to axon
-Physiological transition from graded potential to action potential (AP)
-initial segment - has lowest graded threshold for AP

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4
Q

Axon

A

-Long thin, efferent process
-Many microtubules and microfilaments to maintain shape

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5
Q

Axon transport

A

-Up to 400mm per day

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6
Q

Anterograde transport

A

-Movement of materials (neurotransmitters, proteins, etc) from soma towards synaptic knobs

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7
Q

Kinesin

A

-Protein motor molecule

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8
Q

Retrograde transport

A

-Movement of materials (often waste) from synaptic knobs towards soma

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9
Q

Dynein

A

-Protein motor molecule

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10
Q

What surrounds the axon?

A

-May be surrounded by myelin with nodes of Ranvier

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11
Q

AP conduction speed _________ with _________ diameter & ________myelin.

A

increases, increased, increased

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12
Q

Fibers with largest diameter, most myelin

A

Sensory (afferent) A-alpha
Motor (efferent) Ia, Ib, II
Conduction speed: 70-120m/sec

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13
Q

Fibers in between

A

Sensory (afferent) A-beta
Motor (efferent) III
Conduction speed: 5-30m/sec

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14
Q

Fibers with smallest diameter, least myelin

A

Sensory (afferent) C
Motor (efferent) IV
Conduction speed: 0.5-2m/sec

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15
Q

Synaptic knobs (terminal boutons)

A

-Swelling at end of axons
-Contain structures of synaptic transmission (esp. vesicles of neurotransmitter)

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16
Q

Membrane potential

A

-Due (primarily) to differences in [Na] & [K] between ICF and EFC
-Also [Cl] & [Ca]
-When no signal is being sent = resting membrane potential
[-70mV] varies among neurons & types of neurons

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17
Q

Changes in membrane potential (=information)

A

-Depolarization: toward 0mV
-Repolarization: return from depolarization toward -70mV
-Hyperpolarization (overshoot): more negative than -70mV

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18
Q

Graded (local) potentials

A

-Small, decremental voltage changes in response to some stimulus (receptor, neurotransmitter, etc.)
-Larger stimulus causes larger voltage change (=graded)
-Can be excitatory (depolarizing) or inhibitory (hyperpolarizing)
-Created/located in the dendrites and soma

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19
Q

Action potential (AP)

A

-Huge, stereotypical, non-decremental, unidirectional change in membrane potential that is propagated along axon

20
Q

AP is formed if threshold voltage is met (All or none rule)

A

-Initial segment of axon hillock (site of transition from local potential to AP)
-Threshold varies among neurons, even of the same type (usually around -55mV)

21
Q

Propagation along axons

A

Contiguous or Saltatory

22
Q

Contiguous Conduction

A

-On unmyelinated fibers
-Slower
-Must be recreated on every portion of the membrane

23
Q

Saltatory Conduction

A

-On myelinated fibers
-Much faster
-AP “jumps” from one Node of Ranvier to the next

24
Q

Synapses

A

-Functional connection between neurons
-Usually axodendritic or axosomatic (but can be axoaxonic)
-Usually functions by transforming AP signal into chemical signal (neurotransmitter) that crosses the synaptic cleft

25
Presynaptic neuron
Releases neurotransmitter (sends information)
26
Postsynaptic neuon
Senses neurotransmitter (receives information)
27
EPSP - Excitatory Post-Synaptic Potential
-Depolarizes postsynaptic cell -Moves membrane potential closer to threshold -Makes it more likely to fire an AP
28
IPSP - Inhibitory Post-Synaptic Potential
-Hyperpolarizes postsynaptic cell -Moves membrane further from threshold -Makes it less likely to fire an AP
29
Neurotransmitters
Chemical messengers (hundreds)
30
Excitatory (fast) [neurotransmitter]
Acetylcholine (ACh), glutamate (primarily CNS; estimated at 90%+ of synapses)
31
Inhibitory (fast) [neurotransmitter]
GABA (gamma-aminobutyric acid; mostly brain), glycine (mostly spinal cord)
32
Second messenger mediated (slow; many are either excitatory or inhibitory, depending on receptor)
-Catecholamines (epinephrine & norepinephrine; dopamine) -Serotonin -Neuropeptides (neuromodulators) -Several neurotransmitters have both fast & slow receptors (ACh, glutamate, GABA)
33
Drugs and diseases acting at synapse
-Curare -Botulsim -Tetanus -Myasthenia Gravis
34
Curare
-Toxin that blocks ACh receptors (nicotinic receptors) -Causes flaccid paralysis
35
Botulsim
-Toxin prevents exocytosis of ACh (esp @ neuromuscular junction) -Causes flaccid paralysis
36
Tetanus
-Toxin is transported by retrograde axonal transport to inhibitory neurons of spinal cord -Blocks glycine release -Prevents inhibition of motor neurons; causes spastic paralysis
37
Myasthenia Gravis
-Autoimmune destruction of ACh receptors; although ACh release is normal -Muscle contraction decreases (esp. to repeated contractions) -Causes weakness, double vision, etc.
38
Glial cells
90% by number; 50% by volume
39
Astrocytes (CNS)
-Connective tissue of the CNS -Hold neurons in position -Blood-brain barrier - chemically protect neurons
40
Oligodendrocytes (CNS)
-Myelinate axons in CNS -Larger, myelinate many regions of multiple axons
41
Schwann cells (PNS)
-Myelinate axons in PNS -Smaller, myelinate specific region of one axon -Provide support, myelinate, and have phagocytotic role
42
Ependymal cells (CNS)
-Line ventricles, central canal of the spinal cord -Choroid plexus: specialized ependymal cells within the ventricles that produce CSF -Function: secretory, absorptive and CSF circulatory role
43
Microglia (CNS)
-Phagocytosis of degenerative debris of CNS -Immune function
44
Charcot-Marie Tooth Disease (family of disorders)
-Uncurable; genetic (most common inherited neurological disorder: 40 in 100,000) -Peripheral neuropathy – caused by gap junction channelopathy -Progressive loss of touch sensation, muscle weakness & wasting -Affects longest axons first -(i.e., feet first, then legs, then hands, then arm) -Mechanism/molecule unknown, but causes demyelination of PNS
45
Guillain-Barre Syndrome
-Autoimmune inflammation (after viral infection) where macrophages attack and destroy myelin in the PNS (fairly rare: 1 in 100,000) -Can cause rapid (12 hours! to 2 week) symptoms of weakness, loss of sensation -often affects breathing muscles & patients require ventilation -Patients often recover significantly, but 20% are unable to walk unaided after 6 months
46
Multiple Sclerosis
-Autoimmune attack on CNS myelin (approx. 28 in 100,000) -Symptoms vary widely – depending on specific area of damage -Chronic & debilitating changes in sensation, movement, mood and/or cognition