Chapter 5 (exam 2) Flashcards

1
Q

What is a synapse?

A

Functional contacts between neurons.

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2
Q

What are the types of synapses?

A

Electrical synapses and chemical synapses.

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3
Q

What characterizes electrical synapses?

A

Gap junctions allow cytoplasmic continuity between neurons.

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4
Q

What are connexons?

A

Hemichannels formed by connexins that allow communication between neurons.

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5
Q

How long do connexons typically remain stable?

A

Stable for a couple of hours.

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6
Q

What can pass through large pores of connexons?

A

ATP, nutrients, and second messengers.

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7
Q

What is the speed and directionality of electrical synapses?

A

Fast and bidirectional flow

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8
Q

What is often the configuration of electrical synapses?

A

Often dendrodendritic with no set presynaptic and postsynaptic roles.

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9
Q

What is the typical function of electrical synapses?

A

Typically excitatory, but can also be inhibitory.

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10
Q

Where are electrical synapses commonly found?

A

In breathing and interneurons, such as in the hippocampus.

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11
Q

What was observed in mice without brain connexons?

A

Slight delay in temporal motor precision and inability to distinguish novel from previously seen objects.

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12
Q

What characterizes chemical synapses?

A

Presynaptic neuron releases neurotransmitter into the synaptic cleft.

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13
Q

Where are neurotransmitters typically stored?

A

In vesicles.

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14
Q

What is the active zone in chemical synapses?

A

A specialized area where small molecule neurotransmitters are released.

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15
Q

What is the synaptic cleft?

A

The area of interstitial fluid between presynaptic and postsynaptic neurons

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16
Q

What role do filaments in the synaptic cleft play?

A

They help maintain alignment of presynaptic and postsynaptic neurons.

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17
Q

What do postsynaptic neurons contain?

A

Receptors for neurotransmitters.

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18
Q

What is found in excitatory synapses?

A

Intracellular scaffolding known as postsynaptic density.

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19
Q

What are the typical events in a chemical synapse?

A

AP → VGCC open → neurotransmitter exocytosed in response to elevated Ca2+ → diffuse across cleft → bind to receptor → changes status of ion channel in postsynaptic cell → current generated → neurotransmitter removed → vesicular membrane recovered.

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20
Q

What did Loewi’s experiment demonstrate?

A

Chemical signaling by neurons using frog hearts, vagus nerve, and fluid while monitoring heart beat

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21
Q

What were the conclusions from Katz’s experiments?

A

A specific amount (a quanta) of ACh is spontaneously released, neurotransmitters must be packaged, and calcium plays a role in neurotransmitter release.

depolarization -> End plate potential -> current generated -> action potential (EPP smaller).

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22
Q

What did Boyd and Martin find in their experiments?

A

Distribution of MEPP amplitudes clustered around a single value, confirming neurotransmitters are released in vesicles.

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23
Q

What is the role of calcium in neurotransmitter release?

A

Calcium influx is necessary for neurotransmitter release and postsynaptic depolarization.

Katz used TTX, but an action potential in muscle fiber was still produced

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24
Q

What is the conclusion from studies visualizing Ca2+?

A

Calcium ions are necessary and sufficient for neurotransmitter release.

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25
Q

How are neurotransmitter vesicles released?

A

Via exocytosis.

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26
Q

What did electron microscopy work confirm?

A

The existence of vesicles and the presence of ACh in them.

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27
Q

What is the ‘kiss-and-run’ method?

A

An alternative method of neurotransmitter release that doesn’t involve complete fusion of the vesicle membrane with the axon terminal membrane.

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28
Q

What is the recycling process of synaptic vesicles?

A

A complete cycle includes reserve pool, mobilization, docking, priming, fusion, coating, budding, uncoating, endosome, and loading.

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29
Q

What proteins are involved in vesicle docking and fusion?

A

Synapsin, SNAREs (v-SNAREs and t-SNAREs), and synaptotagmin.

30
Q

What is the role of clathrin in endocytosis?

A

It is the most important protein that attaches to the vesicular membrane.

31
Q

What are the types of neurotransmitter receptors?

A

Ionotropic receptors and metabotropic receptors.

32
Q

What distinguishes ionotropic receptors?

A

Ligand binding site is integral to the receptor molecule and opens an ion channel.

33
Q

What characterizes metabotropic receptors?

A

Ligand binds to G protein coupled receptor, activating intracellular signaling cascades.

Cascade can open pore in protein that is NOT receptor

34
Q

What is an EPSP?

A

Excitatory postsynaptic potential with a reversal potential more positive than threshold.

35
Q

What is an IPSP?

A

Inhibitory postsynaptic potential with a reversal potential more negative than threshold.

36
Q

What factors influence synaptic potentials?

A

Temporal and spatial summation, and glial cell influence.

37
Q

How do glial cells influence synaptic transmission?

A

By stimulating secretion of signaling molecules that bind to receptors on neurons.

38
Q

Where are neuropeptide neurotransmitters released from?

A

More distant locations, not in active zone

39
Q

How can a neurotransmitter be removed (at a chemical synapse)?

A

Glial uptake or enzyme degredation

41
Q

Compare neurons and muscle fibers

A

Muscle fibers need generation of only one end plate potential for contraction, while neurons need multiple stimuli

42
Q

Explain how miniature end plate potentials were discovered by Katz

A

the channels were blocked by drugs that blocked ACh receptors, which shows that MEPPs are stimulated by ACh spontaneously

43
Q

What did Llinas study?

A
  • used volatage clamp of presynaptic and postsynaptic terminal
  • blocking Na+ and K+ channels still had depolarization
44
Q

If you inject Ca2+ into the presynaptic cell, what happens?

A

Depolarization in the post synaptic cell

45
Q

What did biochemical staining show?

A

ACh in vesicles.

Math used to determine number of ACh molecules in vesicle and number needed for MEPP, and they matched

46
Q

True or False: All neurotransmitters are packaged in vesicles

A

False

Nitric oxide and some ATP are not packaged in vesicles

47
Q

True or False: all neurotransmitters packaged in vesicles released through exocytosis

48
Q

Heuser & Reese experiment

A

used horseradish peroxidase to trace vesicle contents (and that they were being recycled)

Horseradish peroxidase enzyme which can break down substrate to yield a color

49
Q

What are all the steps in recycling synaptic vesicles?

A
  1. reservepool
  2. mobilization
  3. docking
  4. priming
  5. fusion
  6. coating
  7. budding
    8.uncoating
    9.endosome
  8. budding
  9. loading
  10. tethered, forming reserve pool
50
Q

Synapsin function

A

tethers loaded vesicles to reserve pool

Phosphorylation of synapsin releases vesicles

51
Q

SNAREs

A
  • receptors for SNAPs
  • Involved in docking, priming, and fusion
52
Q

v-SNAREs

A

attached to vesicle

ex: Synaptobrevin

53
Q

t-SNAREs

A

attached to axon terminal membrane

ex: Syntaxin and SNAP-25 (NOT a “soluble NSF attachment protein/SNAP”)

54
Q

NSF-ATPase

A

regulates SNAREs by binding to SNAPs

55
Q

SNAPS

A

soluble NSF attachment protein

56
Q

Synaptotagmin

A

Binds calcium, leading to conformational changes causing fusion of vesicle and axon terminal membranes

attached to vesicle membrane

57
Q

Munc 13 and munc 18

A

necessary for vesicle exocytosis (facilitate SNARE entwining)

58
Q

Important components endocytosis

A
  • Clathirin: most important protein
  • three-pronged “triskelia” attach to vesicular membrane
  • adaptor proteins (AP-2, AP-180)
59
Q

dynamin

A

GTPase; pinches of clatharin-coated vesicle

60
Q

uncoating of clatharin

A
  • phosphatase (Synaptojanin)
  • chaperones (HSC70 and auxilin)
61
Q

acetylcholine receptor at NMJ experiment

A
  • outside out patch clamp
  • end plate current produced (microscopic inward currents)
63
Q

Voltage clamp with ACh application

A

Macroscopic inward current

64
Q

Voltage clamp myofiber (muscle cell) with electrical stimulation experiment

A

reversal potential not equal to equilibrium of any single ion (determined these experimentally)

65
Q

What happens to reversal potential of you decrease extracellular Na+?

A

shifts left; more negative reversal potential for the channel

65
Q

What happens to reversal potential when you increase extracellular K+?

A

shift right; reversal potential becomes more positive

66
Q

EPSP: Reversal potential (equilibrium potential) more ___ than threshold

67
Q

IPSP: Reversal potential (equilibrium potential) more ___ than threshold

68
Q

Temporal Summation

A

high frequency stimulation at the same synapse

69
Q

Spatial summation

A

simultaneous stimulation at multiple locations

70
Q

How can glial cells influence synaptic transmission?

A
  • Modulate neurotransmitter release
  • Modulate signaling in postsynaptic neuron
  • Role in plasticity
  • Prune synapses