Chapter 5 (exam 2) Flashcards

(71 cards)

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
How are neurotransmitter vesicles released?
Via exocytosis.
26
What did electron microscopy work confirm?
The existence of vesicles and the presence of ACh in them.
27
What is the 'kiss-and-run' method?
An alternative method of neurotransmitter release that doesn't involve complete fusion of the vesicle membrane with the axon terminal membrane.
28
What is the recycling process of synaptic vesicles?
A complete cycle includes reserve pool, mobilization, docking, priming, fusion, coating, budding, uncoating, endosome, and loading.
29
What proteins are involved in vesicle docking and fusion?
Synapsin, SNAREs (v-SNAREs and t-SNAREs), and synaptotagmin.
30
What is the role of clathrin in endocytosis?
It is the most important protein that attaches to the vesicular membrane.
31
What are the types of neurotransmitter receptors?
Ionotropic receptors and metabotropic receptors.
32
What distinguishes ionotropic receptors?
Ligand binding site is integral to the receptor molecule and opens an ion channel.
33
What characterizes metabotropic receptors?
Ligand binds to G protein coupled receptor, activating intracellular signaling cascades. ## Footnote Cascade can open pore in protein that is NOT receptor
34
What is an EPSP?
Excitatory postsynaptic potential with a reversal potential more positive than threshold.
35
What is an IPSP?
Inhibitory postsynaptic potential with a reversal potential more negative than threshold.
36
What factors influence synaptic potentials?
Temporal and spatial summation, and glial cell influence.
37
How do glial cells influence synaptic transmission?
By stimulating secretion of signaling molecules that bind to receptors on neurons.
38
Where are neuropeptide neurotransmitters released from?
More distant locations, not in active zone
39
How can a neurotransmitter be removed (at a chemical synapse)?
Glial uptake or enzyme degredation
40
41
Compare neurons and muscle fibers
Muscle fibers need generation of only one end plate potential for contraction, while neurons need multiple stimuli
42
Explain how miniature end plate potentials were discovered by Katz
the channels were blocked by drugs that blocked ACh receptors, which shows that MEPPs are stimulated by ACh spontaneously
43
What did Llinas study?
- used volatage clamp of presynaptic and postsynaptic terminal - blocking Na+ and K+ channels still had depolarization
44
If you inject Ca2+ into the presynaptic cell, what happens?
Depolarization in the post synaptic cell
45
What did biochemical staining show?
ACh in vesicles. ## Footnote Math used to determine number of ACh molecules in vesicle and number needed for MEPP, and they matched
46
True or False: All neurotransmitters are packaged in vesicles
False ## Footnote Nitric oxide and some ATP are not packaged in vesicles
47
True or False: all neurotransmitters packaged in vesicles released through exocytosis
False
48
Heuser & Reese experiment
used horseradish peroxidase to trace vesicle contents (and that they were being recycled) ## Footnote Horseradish peroxidase enzyme which can break down substrate to yield a color
49
What are all the steps in recycling synaptic vesicles?
1. reservepool 2. mobilization 3. docking 4. priming 5. fusion 6. coating 7. budding 8.uncoating 9.endosome 10. budding 11. loading 12. tethered, forming reserve pool
50
Synapsin function
tethers loaded vesicles to reserve pool ## Footnote Phosphorylation of synapsin releases vesicles
51
SNAREs
- receptors for SNAPs - Involved in docking, priming, and fusion
52
v-SNAREs
attached to vesicle ## Footnote ex: Synaptobrevin
53
t-SNAREs
attached to axon terminal membrane ## Footnote ex: Syntaxin and SNAP-25 (NOT a “soluble NSF attachment protein/SNAP”)
54
NSF-ATPase
regulates SNAREs by binding to SNAPs
55
SNAPS
soluble NSF attachment protein
56
Synaptotagmin
Binds calcium, leading to conformational changes causing fusion of vesicle and axon terminal membranes ## Footnote attached to vesicle membrane
57
Munc 13 and munc 18
necessary for vesicle exocytosis (facilitate SNARE entwining)
58
Important components endocytosis
- Clathirin: most important protein - three-pronged “triskelia” attach to vesicular membrane - adaptor proteins (AP-2, AP-180)
59
dynamin
GTPase; pinches of clatharin-coated vesicle
60
uncoating of clatharin
- phosphatase (Synaptojanin) - chaperones (HSC70 and auxilin)
61
acetylcholine receptor at NMJ experiment
- outside out patch clamp - end plate current produced (microscopic inward currents)
62
63
Voltage clamp with ACh application
Macroscopic inward current
64
Voltage clamp myofiber (muscle cell) with electrical stimulation experiment
reversal potential not equal to equilibrium of any single ion (determined these experimentally)
65
What happens to reversal potential of you decrease extracellular Na+?
shifts left; more negative reversal potential for the channel
65
What happens to reversal potential when you increase extracellular K+?
shift right; reversal potential becomes more positive
66
EPSP: Reversal potential (equilibrium potential) more ___ than threshold
postive
67
IPSP: Reversal potential (equilibrium potential) more ___ than threshold
negative
68
Temporal Summation
high frequency stimulation at the same synapse
69
Spatial summation
simultaneous stimulation at multiple locations
70
How can glial cells influence synaptic transmission?
- Modulate neurotransmitter release - Modulate signaling in postsynaptic neuron - Role in plasticity - Prune synapses