L19 - nerve cells & excitability: action potential Flashcards

1
Q

how do nerve cells communicate?

A

via dendrites, axons and terminals

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2
Q

what does it mean by neurones care polarised?

A

resting membrane potential

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3
Q

what is RMP?

A

electrical charge across plasma membrane where the inside is more negative compared to the outside. -70mV

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4
Q

what are action potentials?

A

change in voltage across membrane

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5
Q

describe depolarisation of membrane

A
  • excitatory signals at dendrites cause ligand gated sodium channels to open
  • causing Na+ ions to diffuse into the cell
  • this decreases the negative charge inside the cell and makes the membrane less negative
  • so cell becomes less polarised
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6
Q

why is axon hillock known as trigger zone?

A
  • influx of Na+ diffuses inside neurone and produces current that travels towards axon hillock
  • a.p usually starts at the axon hillock
  • as a.ps are produced by voltage gated ion channels which are most concentrated at axon hillock
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7
Q

all or none law

A
  • if stimulus is strong enough A.P occurs
  • frequency of A.P rather than strength
  • all A.P same size
  • no weak or strong A.P
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8
Q

hypOpolarisation

A

initial increase of membrane potential to the threshold potential (-55mV)

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9
Q

depolarisation

A

membrane potential goes from resting membrane potential (-70mV) to LESS negative values

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10
Q

overshoot (peak)

A

peak of A.P at +40mV

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11
Q

repolarisation

A

membran potential going back to more negative value (resting memb potential)

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12
Q

hyperpolarisation/ undershoot

A

potential becomes even more negative than RMP

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13
Q

voltage gated ion channels

A
  • closed at RMP
  • open when memb is depolarised (more positive)
  • change in voltage triggers opening
  • close when rmp is restored
  • responsible for initiaiton of Na+ and termination of K+ of action potentials
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14
Q

for A.Ps to be generated what must there be?

A

a signal strong enough to bring membrane voltage to threshold (-55mV), as this is the minimum needed to open voltage gated ion channels

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15
Q

describe how sodium and potassium channels open at threshold

A
  • Na+ channels open quickly
  • K+ channels slowly
  • so initial effect is due to sodium influx
  • causes cell to become even more positive, leading to further depol
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16
Q

describe in depth how A.P is triggered, talk about the channels and how they relate to the graph

A
  • sodium channels open causing influx of Na+ ions to enter cell
  • memb even more depol
  • A.P triggered once men is positive enough
  • by the time sodium channels start to close, K channels are fully opened
  • so K+ ions rush out of cell
  • rmp restored
  • potassium gates slow to close so there is a undershoot called hyperpolarisarion (more neg)
17
Q

absolute refractory period

A

A.P can’t be evoked as voltage gated sodium channels are inactivated and cannot be activated again until memb is depolarised and resting state returns (this is from depol to rmp)

18
Q

relative refractory period

A

memb potential hyperpolarised by potassium ions, AP an be generated only if stimulus is strong enough to overcome the hyperpol to reach the threshold (during hyperpol)

19
Q

action potential propagation

A
  • sodium influx spreads along axon
  • sodium currents diffuse in both directions
  • but refractory properties of ion channels make sure a.p is propagated in ONE DIRECTION
  • as the part that just fired is unresponsive
20
Q

what does the speed of propagation depend on?

A
  • depends on axon diameter (size)
  • and myelination
21
Q

speed of propagation for a large axon

A
  • less resistance to current
  • larger diameter = faster propagation
22
Q

myelin sheath

A
  • electrically insulated axon so currents can jump from node to node
  • as voltage gated sodium and potassium channels are only at nodes of ranvier
23
Q

pain is one of the…

A

slowest sensations bodies can send as they are sent from smaller fibres without myelin

24
Q

faster signals are sent by?

A

larger, myelinated neurones

25
Q

Guillain-barre syndrome

A

destruction of schwann cells in PNS

26
Q

ms

A

loss of oligodendrocytes in brain and spinal column

27
Q

what do ms and Guillain barre syndrome cause?

A
  • muscle weakness
  • numbness
  • tingling
28
Q

when myelin coating of nerves degenerates and the nerves are afferent (sensory)

A
  • signals are diminished
  • or destroyed completely
  • causes numbness & tingling
  • as sensations are not travelling the way they should
29
Q

when myelin coating of nerves degenerates and the nerves are efferent (motor)

A

leads to weakness as brain gives out lots of energy but still can’t actually move the affected limbs. limbs are especially affected as they have longest nerves, longer nerve = more myelin to be destroyed

30
Q

graded potentials

A

-changes in membrane potential in small region of membrsne
- size of potential changes with the strength of stimulus
- if the threshold for sodium channels is reached A.P is generated
- 2 types: excitatory & inhibitory

31
Q

excitatory graded potentials

A

increases likelihood of A.P by depolarising the membrane

32
Q

inhibitory graded potentials

A

decrease likelihood of A.P via hyperpol

33
Q

no summation

A

2 stimuli at separate times

34
Q

temporal summation

A

2 excitatory stimuli occur close in time

35
Q

spatial summation

A

2 stimuli occur at sae time at different locations

36
Q

spatial summation of EPSPs and IPSPs

A

changes in membrane potential can cancel each other out