4 & 5. Resting and Action potentials Flashcards

1
Q

Flux

A

the rate of transfer of molecules

= number of molecules that cross a unit area per unit time e.g. m-2. s-2

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2
Q

Is there net flux in dynamic equilibrium?

A

No

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3
Q

Equilibrium potential

A

The potential at which electrochemical equilibrium has been reached.
Concentration gradient balanced by electrical gradient

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4
Q

When is electrochemical equilibrium achieved?

A

when electrical force prevents further diffusion across the membrane

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5
Q

What does the Nernst equation show?

A

It allows you to calculate the equilibrium potential of a cell (dependent on temperature and charge)

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6
Q

What are the intracellular and extracellular concentrations of the 4 main ions involved in action potentials?

A

Na+: inside: 10 outside: 150
K+: inside: 150 outside: 5
Cl-: inside: 5 outside: 120
Ca2+: inside: 0.1 outside: 2

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7
Q

Explain why the resting membrane potential of most cells is around -70 mV

A

Equilibrium potential of K+ is -90 mV and Na+ is +72
Membranes have mixed K+ and Na+ permeability
But more permeable to K+ so resting membrane potential is closer to equilibrium potential of K+.

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8
Q

What does the Goldman-Hodkin-Katz equation show?

A

Accounts for relative permeability of the membrane at any one time to different ions so you can figure out the resting membrane potential.

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9
Q

Resting potential

A

-70mV

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10
Q

Depolarising

A

-70 to 0 (becoming more +)

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11
Q

Hyperpolarising

A

-70 to -90 (becoming more -)

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12
Q

Overshoot

A

0 to +

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13
Q

Repolarising

A

+ to -

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14
Q

What is the difference between graded potentials and action potentials?

A

APs are an all-or-nothing event (have the same amplitude every time)
GPs can vary in amplitude and the amplitude is affected by the strength of the stimulus. GPs can be positive or negative and they decrease in altitude as they travel away from the point of origin.

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15
Q

How can nerve cells use graded depolarisations and hyperpolarisations for signalling?

A

Contribute to initiating or preventing action potentials

May summate or cancel each other out, create a more integrated signal

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16
Q

Where do graded potentials occur?

A

Synapses

Sensory receptors

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17
Q

Where do action potentials occur?

A

In excitable cells
Mainly neurones and muscle cells e.g. in muscle cells lead to contraction
Also in some endocrine tissues e.g. In B cells of pancreas provoke release of insulin

18
Q

What does permeability to ions depend on?

A

Conformational state of ion channel

Most channels in neurology are voltage operated

19
Q

What are the 5 phases of an action potential?

A
  1. Resting membrane potential
  2. Depolarising stimulus
  3. Upstroke
  4. Repolarisation
  5. After hyperpolarisation
20
Q

Describe phase 1 of an action potential

A

Caused by K+ moving out of cells
Finite permeability to Na+
Membrane potential nearer equilibrium potential for K+ than for Na+

21
Q

Describe phase 2 of an action potential

A

Stimulus depolarises membrane potential
(Graded response- small and slow depolarisation)
Moves it in +ve direction towards threshold

22
Q

Describe phase 3 of an action potential

A

Starts at threshold potential
At threshold potential lots of Na+ channels respond
PNa increases because voltage-gated Na+ channels open quickly
Na+ ions enter the cell down their electrochemical gradient
Depolarisation
Membrane potential moves toward Na+ equilibrium potential
PK increases as the voltage-gated K+ channels start to open slowly
K+ ions leave the cell down their electrochemical gradient
(Slowly- Less than Na+ entering)

23
Q

Describe phase 4 of an action potential

A

PNa decreases because voltage-gated Na+ channels inactivate (Channels blocked)
Na+ entry stops
PK increases as more voltage-gated K+ channels open and remain open
K+ leaves the cell down its electrochemical gradient
Membrane potential moves toward the K+ equilibrium potential

24
Q

Describe phase 5 of an action potential

A

(At rest) voltage-gated K+ channels are still open
K+ continues to leave the cell down the electrochemical gradient
Membrane potential moves closer to the K+ equilibrium
Additional K+ channels are still open, so slight hyperpolarisation (Close slowly)
Some voltage-gated K+ channels then close

Membrane potential returns to the resting potential

25
Q

What occurs at the start of repolarisation?

A

Part of channel protein reacts to change in voltage
and blocks the channel so Na+ cant get through
Na+ channel gate is open, but blocked by inactivation protein
Na+ entry to cell stops
Depolarisation recognised by K+ channels and more open

26
Q

What is the underlying mechanism for the absolute refractory period? What is this?

A

Na+ channel inactivation is the underlying mechanism for
the Absolute refractory period
Inactivation gate is closed
New AP cannot be triggered even with very strong stimulus

27
Q

What happens later in repolarisation?

A

Absolute refractory period continues
Na+ Channel activation gate closes
Inactivation protein still present

28
Q

What occurs during post-hyperpolarisation?

A

Relative refractory period
Inactivation gate is open
Stronger than normal stimulus required to trigger an action potential

29
Q

How long does a normal action potential last?

A

2 ms

30
Q

Threshold potential

A

Once this potential is reached an AP is triggered

31
Q

Refractory state

A

Unresponsive to threshold depolarization

32
Q

What is the regenerative relationship between PNa+ and membrane potential?

A

Once threshold is reached the cycle continues
Positive feedback behaviour
Cycle continues until the voltage-gated Na+ channels inactivate- closed and voltage-insensitive
Membrane remains in a refractory (unresponsive) state until the voltage-gated Na+ channels recover from inactivation

33
Q

Ion channels vs Ion pumps in an action potential

A

Ion channels: Main pathway for ion movement, rapid

Ion pumps: NOT directly involved in ion movement during an AP, slow, need ATP

34
Q

Why can the AP only move in 1 direction?

A

Originating area is refractory

35
Q

Nodes of ranvier

A

Unmyelinated gaps along the axon
Allow rapid impulse propagation as impulse can jump to areas of high concentration of Na+ channels
Allows movement via saltatory conduct

36
Q

What influences conduction velocity?

A

Axon diameter

Axon myelination

37
Q

Large diameter myelinated axons speed

A

120 m/s

Low internal resistance

38
Q

Small diameter non-myelinated axons speed

A

1 m/s
Can’t travel by saltatory conduct
High internal resistance

39
Q

How does conduction velocity change with increased axon diameter?

A

Increases

Less resistance to current flow inside large diameter axons

40
Q

How does conduction velocity change with myelination?

A

Increases

AP’s only occur at nodes of Ranvier

41
Q

What slows conduction velocity?

A

Reduced axon diameter (i.e. re-growth after injury)
Reduced myelination (i.e. MS and diphtheria)
Cold, anoxia, compression and drugs (some anaesthetics)