action potentials Flashcards

1
Q

Difference between action potentials and electrotonic potentials

size?
speed?
lasting?
graded?

A
Electrotonic potential:
Small (1-15mV)
Slow depolarisation
Slow decay
Graded
Action potential:
Large (~100mV)
Rapid depolarisation
Rapid repolarisation
All-or-nothing
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2
Q

Normal arrangement of Na+ channel before any potential arrives

the two gates?

A

activation gate = held closed at rest (voltage sensitive domain attracted to -ve charge)

Inactivation gate = help open at rest

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3
Q

What happens when electronic potential arrives?

A

the membrane will slightly depolarise -> could be due to excitatory synaptic input

as it is an electronic potential -> the activation gate is still stromg enough to hold the gate closed

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4
Q

If a big electronic potential arrives that can hit threshold

effect of this? why?

A

The force holding the gate closed isn’t strong enough hence the gate springs open
Na+ flows into the cell -> depolarises the cell

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5
Q

What makes an action potential all or nothing?

what does Na+ influx lead to?

A

the initila depolaristaion that reach threshold and caused the Na channel to open will lead to Na+ influx which causes further depolarisation and channels opening and more influx hence a positive feedback mechanism

Positive feedback ensures rapid activation of all available channels (PNa increases x100)

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6
Q

How is Na+ channel shut?

why can’t activation gate close?
what happens instead?

A

Activation gate cannot close - it is powerfully attracted to the outside of membrane

BUT inactivation gate is now pulled close because it is attracted to the outside hence prevents Na+ influx

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7
Q

Why is K+ channels opening delayed?

A

gives time for AP to hit peak with Na+ channels opening

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8
Q

absolute refractory period

what does this mean? why?

A

Na+ channels are inactive at this point and can’t reset themselves till threshold gets below threshold

Blocked by inactivation gate hence this keeps each AP a separate + individual event

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9
Q

relative refractory period

what does it take time to do?
what can take place but is harder?

A

cell is hypppolarising and takes time for the cell to get back to normal resting potential

takes a stronger stimulus to get it up to threshold so it can fire AP but less likely to do so

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10
Q

Important Principles of APs

what opens?
what does this lead to? effect of this?
what stops depolarisation?
what repolarises?

A

Voltage-gated Na+ channels are opened by depolarisation above a threshold value (~ -50Mv)

Positive feedback ensures that the permeability to Na+ is briefly far higher than to K+, ensuring very rapid, all-or-nothing depolarisation

To stop the depolarisation, the vgNa channels inactivate and while they are inactivated the cell cannot fire another AP

To repolarise, voltage gated K+ channels open and carry the excess positive charge back out of the cell

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11
Q

Why do we need Aps

A

Because nerve cells have to communicate over long distances

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12
Q

How do Aps travel distances?

what happens along axon?

A

Aps propagate hence replicate themselves

The electric current will spread further as the next bit of axon will hit the threshold and fire AP so the elextronic potentials are pushed further and further down the membrane

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13
Q

Why do Aps travel in one direction?

A

Ap moves in 1 direction as first AP goes into refractory period so the ap goes down the axon

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14
Q

How to increase the speed of AP propagation? (3)

A

larger diameter

low membrane permeability (good insulation) e.g. myelin sheath

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15
Q

Myelin sheath

what kind of conduction? how?
if damaged what happens?

A

The myelin sheath greatly increases the speed of action potential propagation
salvatory conduction as it jumps from node of ranvier
If myelin sheath is damaged, AP transmission may be delayed or completely blocked

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16
Q

Multiple Sclerosis: loss of myelin

what does MS attack? so where does it affect?
effect of this?

A

Multiple Sclerosis attacks the myelin sheath (oligiodendrocyte) cells so it will demyelinate axons in the CNS (doesn’t affect peripheral nerves) so one node won’t reach the next node

therfore can slow down signals or even have complete blockage of signals flowing through those axons

Plaques can occur anywhere in the CNS white matter
Producing sensory, motor, cognitive or behavioural deficits