Synaptic Transmission and the Neuromuscular Junction Flashcards

1
Q

List the staged of an AP passing to muscle

A
  1. AP comes down axon to neuromuscular junction.
  2. Ca2+ channels open, Ca2+ influx.
  3. Ca2+ binds to synaptotagmin.
  4. Vesicle brought close to membrane.
  5. Snare complex make a fusion pore.
  6. Transmitter ACh released through pore.
  7. Ach binds nicotinic ACh receptor channels on muscle end-plate = conformational change.
  8. channel opens, Na+ influx.
  9. depolarisation, will also activate adjacent Na+ channels.
  10. = muscle end-plate potential.
  11. Ach esterase degrades Ach
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2
Q

How can higher levels of neurotransmitter be released?

A

Size of AP cannot increase, however frequency can = increase Ca2+ conc = more transmitter released

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3
Q

Describe Ca2+ voltage-gated channels

A

Very similar to Na+ channels. 4 subunits, Voltage sensing domain. L type = target of many drugs, can be blocked – stopped release of Ca – less response. Channels activate/inactivate slower then Na+ channels

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4
Q

What are the 2 ways to block an nACh receptor?

A

Competitive blocker: binds, closing channel e.g. d-tubocurarine = paralysis

Depolarising blocker: binds closing then opening channel that is now desensitised to neurotransmitter e.g. succinylcholine (short-acting muscle relaxant and local anaesthetic)

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5
Q

Give a clinical example where an action potential cannot occur

A

Myasthenia gravis –> autoimmune disease targeting nACh receptors = release of Ach is fine, but as the receptors are damaged, no Na+ K+ entry = no depolarisation = weakened end-plate potential

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6
Q

What type of Ca2+ channel is important and why?

A

L type = target of many drugs, can be blocked – stopped release of Ca – less response

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7
Q

What is a neuromuscular junction?

A

synapse between nerve and skeletal muscle fibre

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8
Q

What enzyme breaks down ACh?

A

acetylcholine esterase

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9
Q

What is the gap between the presynaptic nerve membrane and postsynaptic muscle membrane called?

A

synaptic cleft

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10
Q

How can competitive blocking by d-tubocurarine be overcome?

A

increasing ACh conc

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11
Q

Outline the difference between an Ca2+ and Na+ channel

A

Na+ in/active faster

Ca+ channels open at more +ve MP

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12
Q

What does a muscle end-plate potential result in?

A

propagation of an AP along the muscle fibre

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13
Q

What does depolarisation at the end of a neuron cause?

A

opening of Ca2+ voltage-gated ion channels = Ca2+ inward

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14
Q

DHP (dihydropyrdines) block what type of Ca2+ channel?

A

L-type

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15
Q

What is Ca2+ channel inactivation dependent on?

A

Ca2+ conc inside the cell

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16
Q

What is the difference between a nicotinic and muscarinic AChR

A

nicotinic = ligand-gated

muscarinic = GCPRs

17
Q

When referring to an AP what is meant by all or nothing?

A

once threshold has been reached the AP will be fired and conducted along the whole length of the nerve or not at all

18
Q

What is an inactivated channel?

A

one that is open but ions cant travel through