Changing Membrane Potentials Flashcards

1
Q

Give examples of how changes in membrane potentials are used.

A

Action potentials in nerve and muscle cells
Triggering and control of muscle contraction
Control of secretion of hormones and neurotransmitters
Transduction of sensory information into electrical activity by receptors
Postsynaptic actions of fast synaptic transmitters

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2
Q

Define depolarisation.

A

A decrease in the size of the membrane potential from its normal value. This means that the membrane potential becomes less negative and therefore the cell interior becomes less negative.

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3
Q

Define hyperpolarisation.

A

An increase in the size of the membrane potential from its normal value. This means that the membrane potential is more negative and therefore also the cell interior is more negative.

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4
Q

How can the membrane potential be changed?

A

By changing the selective ionic permeability of an ion. For example increasing the membrane permeability for K+ means that K+ will leave the cell due to the concentration gradient. This will make the cell interior more negative and therefore cause hyperpolarisation.

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5
Q

How can you increase the membrane permeability for an ion?

A

By opening channels.

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6
Q

How does the membrane permeability relate to the equilibrium potential?

A

Increasing membrane permeability for an ion shifts the membrane potential towards the equilibrium potential of the ion.

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7
Q

What will happen if you open channels for K+?

A

Hyperpolarisation and MP will move towards -95mV.

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8
Q

What will happen if you open channels for Cl-?

A

Cl- will move into the cell. Cause hyperpolarisation and MP will move towards -96mV.

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9
Q

What is the equilibrium potential of sodium?

A

+70 mV

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10
Q

What is the equilibrium potential of Ca2+?

A

+122 mV

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11
Q

What will happen if you open channels for sodium?

A

Sodium will enter the cell and cause depolarisation and MP will move towards Ena which is +70mV.

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12
Q

What will happen if you open channels for Ca2+?

A

Calcium will enter the cell and cause depolarisation and MP will move towards Eca which is +122mV.

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13
Q

Give an example of a channel that is not perfectly selective.

A

Nicotinic acetylcholine receptors with their channels are not perfectly selective to Na+. Also Ca2+ and K+ can pass through.

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14
Q

Why can’t Cl- pass through the nicotinic acetylcholine receptor channel?

A

Because the pore is negative, it would not work.

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15
Q

What is the consequence of the nicotinic acetylcholine receptor channel letting Na+ and other cations in?

A

An increased permeability for those ions means that depolarisation will occur and move the membrane potential towards 0mV. An intermediate between Ena and Ek

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16
Q

What types of gating are there?

A

Ligand gated
Voltage gated
Mechanical gated

17
Q

How are ligand gated channels regulated?

A

By a signalling messenger (ligand)

Also by intracellular messengers like IP3

18
Q

How are voltage gated channels regulated?

A

The channels either open or close in response to changes in the membrane potential and therefore involved in action potentials.

19
Q

What is fast synaptic transmission?

A

When the receptor protein is also an ion channel.

20
Q

What is slow synaptic transmission?

A

When the receptor protein and the channel are two separate proteins.

21
Q

Give examples of synaptic transmissions. Where do they occur?

A

Nerve to nerve cell
Nerve to muscle cell
Nerve to gland cell
Sensory to nerve cell

22
Q

What is excitatory post-synaptic potential?

A

When a transmitter opens a ligand-gated channels that causes membrane depolarisation. It brings the membrane potential closer to the threshold for action potential.

23
Q

Give examples of transmitters that are responsible for EPSP.

A

Acetylcholine and glutamate

24
Q

What is inhibitory post-synaptic potential?

A

Inhibitory transmitters that open ligand-gated channels that cause hyperpolarisation. It takes the membrane potential further away from the threshold for action potential.

25
Q

Give examples of transmitters that are responsible for IPSP.

A

Glycine and GABA

26
Q

Give examples of slow synaptic transmission.

A

Direct g-protein gating.
Gating via an intracellular messenger by GPCR and a signalling cascade. An example can be adrenaline binding to b1-adrenoceptors in the heart.

27
Q

What other factors can influence membrane potential?

A

Changes in the ion concentration. For example increasing plasma concentration of K+ will lead to an influx of K+ into the cell and therefore depolarisation. This makes the cell more excitable.
Electrogenic pumps like Na+K+ATPase..