ICPP 5 Flashcards

1
Q

What determines whether an action potential is generated in an axon hillock?

A

Whether summation of EPSP and IPSP reaches threshold potential.

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2
Q

What happens to the membrane potential of an ion if the conductance is increased?

A

The membrane potential will move closer to the equilibrium potential.

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3
Q

What happens during the upstroke of an action potential?

A

Na+ channels open and Na influx depolarises cell to threshold level which causes more Na+ channels to open…

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4
Q

What happens during the downstroke of an action potential?

A

Na+ channels close and become inactivated.

K+ channels open, K+ efflux returns membrane potential to resting.

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5
Q

What is hyperpolarisation?

A

When the membrane potential is lower than resting level due to more K+ channels being open.

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6
Q

What causes hyperpolarisation?

A

Slow closing of the K+ channels

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7
Q

How do sodium channels become re-activated?

A

Inactivation pore inactivates them, this is only removed when the membrane becomes hyperpolarised and the channel then closes.

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8
Q

What is the absolute refractory period?

A

When the sodium channels are all inactivated. No matter how strong a stimulus, an AP cannot be generated.

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9
Q

How is the relative refractory period different to the absolute refractory period?

A

In RRP, Na+ channels are recovering from inactivation, so if a stimulus is large enough then an AP may be generated.

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10
Q

How many polypeptides are there in 1 functional Na+ channel?

A

1

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11
Q

Outline the structure of a voltage gated Na+ channel.

A

1 polypeptide with 4 domains.
Each domain has voltage sensor in transmembrane spanning region 4.
Between the 3rd and 4th domain there is an inactivation particle.
There is a p region which dictates which ion channel flows through.

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12
Q

How do voltage gated K+ channels differ?

A

4 polypeptides make up 1 functional channel.

No inactivation particle.

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13
Q

What is the mechanism of action of local anaesthetics?

A

They block Na+ channels, stopping action potential generation in pain fibres.

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14
Q

What order do local anaesthetics block axons?

A
  1. Small myelinated
  2. unmyelinated
  3. Large myelinated
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15
Q

Local anaesthetics work in a use-dependent manner, explain this.

A

They block the ion channel more easily when it is open

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16
Q

True or false: smaller axon diameter will increase conduction velocity.

A

False.

Larger diameter leads to increased velocit.

17
Q

How is AP conducted along an axon?

A

Change in MP causes a local current spread, which causes an immediate local MP change. If this threshold potential then an AP will fire.

18
Q

What 3 properties lead to a high conduction velocity of an axon?

A
  1. High membrane resistance
  2. Low membrane capacitance
  3. Large diameterq
19
Q

What does low resistance suggest?

A

More channels are open, more local current lost.

20
Q

What is capacitance?

A

The ability to store charge

21
Q

High resistance means…

A

Fewer ion channels open, so less charge lost..

22
Q

Myelination of axons increases conduction velocity. How?

A

Reduces capacitance and increases resistance

23
Q

What 2 special cells form myelin?

A
  1. Oligodendrocytes in CNS

2. Schwann cells in PNS

24
Q

What is saltatory conduction?

A

No AP needs to be generated in insulated, intermodal space, so it jumps between nodes of ranvier which have high density of Na+ channels.

25
Q

Give an example of a demyelinating disease.

A

Multiple Sclerosis.

Auto-immune disease which destroys myelin..decreasing conduction velocity or completely blocking AP transmission.

26
Q

What is a neuromuscular junction?

A

Synapse between a nerve and a skeletal muscle fibre.

27
Q

What channels are present at the nerve terminal?

A

Na+ channels, K+ channels and Ca2+ channels.

28
Q

What does depolarisation in the nerve terminal cause?

A

voltage gated calcium channels open, influx of calcium causes neurotransmitter release.

29
Q

How can you increase the amount of neurotransmitter released?

A

Increased frequency of action potentials. All the same size as all or nothing.

30
Q

Is the structure of the voltage gated calcium channel most similar to a Na+ channel or K+ channel?

A

Na+ channel. 1 polypeptide and 4 domains.

31
Q

What is MOA of dihydropyridines?

A

L-type calcium channel blocker. Decrease blood pressure.

32
Q

Which proteins are involved in the exocytosis of neurotransmitters?

A

Synaptotagmin - binds to the calcium and brings vesicle to membrane.
Snare complex- forms a fusion pore at membrane.

33
Q

Name a competitive nAChR blocker?

A

Tubocurarine

34
Q

name a depolarising nAChR blocker and outline its MOA.

A

Succinylcholine. It binds to the receptor and causes depolarisation, however it doesn’t dissociate, so the membrane cannot hyperpolarise again which means the Na+ channels cannot activate.

35
Q

What is myasthenia gravis?

A

Autoimmune disease targeting nACh receptors.