3. Synaptic Transmission Part 1 Flashcards

1
Q

type of synapse where current flows directly from one cell to another through connexons

A

electrical synapse

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2
Q

type of synapse with secretion of a specific chemical by a nerve terminal and its interaction with specific postsynaptic receptors

A

chemical synapse

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3
Q

at an electrical synapse, the distance between pre and post synaptic cell membranes is:

A

~3.5nm

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4
Q

at electrical synapses, the agent of information transmission is:

A

ionic current

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5
Q

is there synaptic delay between electrical synapses?

A

no

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6
Q

is signal transmission unidirectional or bidirectional in electrical synapses?

A

usually bidirectional

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7
Q

at electrical synapses, there is _____ between the cells

A

cytoplasmic continuity

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8
Q

composed of 6 connexins and form the gap junction

A

connexon

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9
Q

gap junctions and connexons are more common during:

A

embryonic development

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10
Q

if current injection into either cell A or cell B results in the depolarization in both cells, the cells are:

A

electrically coupled

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11
Q

at chemical synapses, the distance between pre and post synaptic cell membranes is:

A

20-40nm

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12
Q

is there cytoplasmic continuity between cells at chemical synapses?

A

no

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13
Q

at chemical synapses, current flows via:

A

activation of receptors and the consequent opening of postsynaptic ion channels

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14
Q

at chemical synapses, the agent of information transmission is a:

A

chemical transmitter

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15
Q

is there synaptic delay at chemical synapses?

A

yes (~1-5ms)

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16
Q

is signal transmission unidirectional or bidirectional in chemical synapses?

A

unidirectional

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17
Q

many synapses occur on dendrites and dendritic spines, and these are usually:

A

excitatory synapses

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18
Q

some synapses occur on dendrites closer to the cell body, and on the cell body itself, these are usually:

A

inhibitory synapses

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19
Q

true or false: synapses occur randomly

A

false

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20
Q

where is the postsynaptic density found?

A

at both excitatory and inhibitory synapses

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21
Q

provides a structural matrix which clusters ion channels and anchors signalling molecules such as kinases and phosphatases

A

the post synaptic density (PSD)

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22
Q

the post-synaptic density is a general organizer of the:

A

postsynaptic signal transduction machinery

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23
Q

links regulatory molecules to their targets, and coordinates developmental and activity-dependent changes in postsynaptic structures

A

the postsynaptic density (PSD)

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24
Q

one of the earliest models to examine muscle function

A

neuromuscular junction (NMJ)

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25
Q

action potentials at the neuromuscular junction (NMJ) are dependent on the release of:

A

acetylcholine (ACh)

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26
Q

located inside the nerve terminal of neuromuscular junctions and contains vesicles of neurotransmitters

A

active zones

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27
Q

synapses in the peripheral nervous system (PNS) are found at the:

A

neuromuscular junction (NMJ)

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28
Q

a plant alkyloid that binds to and blocks nicotinic ACh receptors; it prevents nerve transmission at the neuromuscular junction

A

curare (or tubocurarine)

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29
Q

tubocurarine is a _____ that binds to the same site as ACh

A

reversible competitive antagonist

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30
Q

curare blocks neuromuscular transmission by blocking the activation of:

A

ACh receptors at the neuromuscular synapse

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31
Q

go review slide 154

A

wahooooo

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32
Q

the process of passing a weak electrical current through the synapse

A

ionophoresis

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33
Q

as ACh is ionophoresed further from the synapse, the post synaptic potential (PSP) becomes:

A

weaker

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34
Q

mapping the distribution of ACh sensitivity using ionophoresis suggests that:

A

the ACh receptors are very close to, if not directly at the neuromuscular synapse

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35
Q

found at very high concentrations at the folds of the cleft of the neuromuscular junction (~10 000 per um^2)

A

ACh receptors

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36
Q

found at the base of the folds of the neuromuscular junction

A

voltage gated Na+ channels

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37
Q

at the neuromuscular junction, ACh binds to and activates the:

A

nicotinic acetylcholine receptor (nAChR)

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38
Q

once the nicotinic acetylcholine receptor (nAChR) is activated, the receptor allows ____ to flow into the cell and ____ to flow out of the cell

A

Na+ ions, K+ ions

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39
Q

why does the synpatic current at the neuromuscular junction have a reversal potential of ~0mV?

A

because the nicotinic receptor channels (nAChRs) allow both Na+ and K+ ions to flow

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40
Q

the current at the neuromuscular junction is a summation of:

A

the individual currents through each nAChR channel

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41
Q

the current at the neuromuscular junction is also known as the:

A

endplate current (it has a very sharp onset which is followed by an exponential decay)

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42
Q

what causes the sharp onset of the endplate current?

A

all of the channels are activated nearly simultaneously

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43
Q

what causes the exponential decay of the endplate potential?

A

the channels close in a stochastic (random) function: some close quickly and the others take longer

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44
Q

what are the three major neurotransmitters found in the CNS?

A

glutamate, glycine, GABA

45
Q

what is the difference between ionotropic vs metabotropic receptors?

A

ionotropic receptors are ligand gated, and metabotropic receptors are GPCRs

46
Q

what are the three major types of glutamate receptors?

A
  • NMDA
  • AMPA
  • kainate
47
Q

true or false: several types of glutamate receptors may be found at a single synapse

48
Q

the subunits of ionotropic receptors may have _____ each, and usually _____ subunits assemble to form a functional receptor

A

3-4 transmembrane regions, five

49
Q

how many glutamate molecules are needed to activate the AMPA receptor?

A

2 (but can bind up to 4)

50
Q

how many AMPA receptor subunits are there?

A

4 (GluR1-GluR4)

51
Q

which subunit of the AMPA receptor confers Ca++ impermeability

52
Q

the GluR2 subunits make the AMPA receptors impermeable to:

53
Q

which site of the GluR2 subunit is responsible for Ca++ permeability?

A

the Q/R site (this is an arginine in GluR2 but a glutamine in GluR1, 3, and 4)

54
Q

Ca++ permeable AMPA receptors are involved in:

A

epilepsy, ALS, pain and addiction (reward centres)

55
Q

GluR2 subunits have a(n) ____ residue at the Q/R site

56
Q

NMDA receptors are composed of:

A

2 NR1 subunits and 2 NR2 subunits

57
Q

glutamate binds to the _____ subunits of the NMDA receptors

58
Q

glycine binds to the _____ subunits of the NMDA receptors

59
Q

how many molecules of glutamate and glycine are needed to required for activation of the NMDA receptor?

A

two molecules of glutamate and two molecules of glycine

60
Q

at resting potentials, NMDA receptors are blocked by:

A

external Mg++

61
Q

NMDA receptors act as _____ because they require both neurotransmitters and cell depolarization to be activated

A

coincidence detectors

62
Q

true or false: the properties of the various NMDA receptor subtypes can very significantly

63
Q

inhibitory fast synaptic transmission is mediated through the activation of:

A

glycine and GABA receptors

64
Q

glycine and GABA receptors allow ____ to flow across the cell membrane

65
Q

all known glycine receptors are:

A

ionotropic

66
Q

glycine receptors are composed of:

A

five subunits

67
Q

native glycine receptors (GlyRs) are complexes of different combinations of:

A

alpha subunits, beta subunits, and a scaffolding protein known as gephyrin

68
Q

homomeric glycine receptors are composed of:

A

five alpha subunits

69
Q

heteromeric glycine receptors are composed of:

A

two alpha subunits and three beta subunits

70
Q

how many types of alpha subunits for the glycine receptor are there?

71
Q

how many types of beta subunits for the glycine receptor are there?

72
Q

neonatal animals express the ____ subunit on their glycine receptors, but this changes throughout development such that older animals express the ____ subunit

A

alpha two, alpha one

73
Q

how does glycine activate the glycine receptors (GlyRs)?

A

glycine binds to the interface between the alpha and beta subunits

74
Q

how many molecules of glycine are required for activation of glycine receptors (GlyRs)?

A

at least 2

75
Q

a potent antagonist of glycine receptors (GlyRs) is:

A

strychnine (rat poison)

76
Q

what is the difference between glycine receptors containing alpha two subunits and glycine receptors containing alpha one subunits?

A

alpha two subunits have a longer mean open time

77
Q

what are the two major kinds of GABA receptors?

A

1) ionotropic (GABAa and GABAc)
2) metabotropic (GABAb)

78
Q

list two GABAa antagonists that bind to and reduce GABA IPSPs

A

picrotoxin and bicuculline

79
Q

picrotoxin is a:

A

GABAa pore blocker

80
Q

bicuculline is a:

A

GABAa competitive antagonist

81
Q

both picrotoxin and bicuculline cause:

A

convulsions

82
Q

addictive drugs which lengthen the open time of GABAa receptor channels

A

barbituates

83
Q

non-addictive drugs that increase the number of GABAa receptor channels opening

A

benzodiazepines (diazepam/valium)

84
Q

drug which binds to GABAa receptors and potentiates IPSPs and leads to calming and sedation

85
Q

activation of neonatal GABA receptors depolarize the cell membrane and leads to the unblocking of:

A

NMDA receptors

86
Q

true or false: equilibrium potential for Cl- changes during development

87
Q

GABA is _____ in neonates and _____ in adults

A

excitatory, inhibitory

88
Q

in neonates, high levels of _____ ensures that Cl- concentrations are high inside the cell

A

the NKCC1 transporter

89
Q

in more mature organisms, _____ levels are low and _____ becomes highly expressed to ensure that Cl- concentrations inside the cell are low

A

NKCC1, KCC2

90
Q

the equilibrium potential of Cl- in neonates is:

91
Q

go review slides 184-186

A

you can do it!

92
Q

inhibitory synapses are usually located closer to the cell body, while excitatory synapses are located further away from the cell body along more distal dendrites, this ensures that:

A

EPSPs can be reduced or shunted before they get to the AP initiation zone

93
Q

what are the two mechanisms of inhibition?

A

1) maintaining the membrane potential away from threshold via increasing the Cl- or K+ conductance
2) shunting inhibition, where the EPSP is ‘reduced’ and is not strong enough to depolarize the cell to threshold

94
Q

consists of two large axons that form a chemical synapse

A

stellate ganglion of the squid

95
Q

there must be some presynaptic depolarization if we are to get a:

A

postsynaptic potential change

96
Q

a big molecule that cages Ca++ so that is cannot interact with cell components

97
Q

an increase in _____ is all that is needed to cause neurotransmitter release

98
Q

we only need _____ to open voltage-gated Ca++ channels

A

presynaptic depolarization

99
Q

the minimum amount of neurotransmitter that can be released

A

one quanta (one vesicle)

100
Q

is it possible for there to be release of neurotransmitters into the synaptic cleft in the absence of a presynaptic AP?

A

yes (called spontaneous release)

101
Q

spontaneous release of neurotransmitters leads to:

A

miniature PSPs (or miniature endplate potentials at the NMJ)

102
Q

transmitter release occurs through the fusion of vesicles with the:

A

presynaptic membrane

103
Q

veiscle recycling near the active zone occurs with the aid of:

A

clathrin-coated pits

104
Q

what are the major proteins involved in vesicle fusion to the cell membrane?

A

SNARES (snap receptors)
- v-SNAREs (vesicle snares)
- t-SNAREs (membrane proteins)

105
Q

vesicle docking, fusion, and release of neurotransmitters involves the:

A

SNARE complex

106
Q

Ca++ binds to synaptotagmin (v-SNARE) and triggers:

A

membrane fusion

107
Q

how do SNAREs work?

A

interaction of the SNARE proteins brings the vesicle and presynaptic membrane closer together

108
Q

go review slide 199

A

I’m just too lazy to write it all down