CSB332H1 Lecture Notes - Lecture 8: Axon Hillock, Myelin, Voltage Clamp

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coraleel39

25 Feb 2014

School

UTSG

Department

Cell and Systems Biology

Course

CSB332H1

Professor

Francis Bambico

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Document Summary

An action potential is brought about by the opening of voltage-gated na+ channels and the opening and closing of k+ channels. An action potential is regenerative because it produces a chain reaction. When a voltage-gated na+ channel is opened by changes in membrane potential, As more na+ ions move into the neuron, the more the neuron gets depolarized. Greater depolarization would eventually open up some more voltage-gated na+ channels that are sensitive to the depolarization value. Initiation is when a threshold membrane potential is achieved. Voltage-gated calcium channel doesn"t do much in a typical mammalian neuron, but it is important in heart functions. Voltage-gated sodium channel: the pore forming region of the ion channel is formed between s5 and s6. The p-loop is the pore formation region of the ion channel. Voltage-gated potassium channel: the k+ channel signature sequence is a sequence of amino acids that is different from the sequence in the na+ channel.

Related Questions

This is the peak depolarization in an action potential. At this point in an action potential two events start to happen.

1. Na+ channels begin to inactivate, which is equivalent to closing.

2. A majority of the K+ channels are beginning to open.

Determine what happens to the membrane potential when voltage-gated K+ channels are open simultaneously with voltage-gated Na+ channels (and the leak K+ channels which are still open). Increase the membrane permeability to K+ by increasing it to 115.

i. What happens to the membrane potential Em? __________________________

j. Why does the membrane potential change in this direction? __________________________ Now inactivate the voltage-gated Na+ channels by reducing the membrane permeability for Na+ back to 1. k. What is the new membrane potential? _____________

l. Is the new membrane potential less negative or more negative than the resting membrane potential listed in line âbâ of this section? _____________

m. Why? (hint: what 2 types of K+ channels are open now?) n. Under the current ionic concentrations given, what is the most negative value that the membrane potential could reach? _____________ (Increase the permeability of the membrane to K+ to confirm your answer.)

o. What equilibrium potential has the same value? _____________

p. At this point in the action potential, when the membrane potential is more negative than the resting potential, the membrane potential is said to be hyperpolarized. What happens to voltage-gated K+ channels (membrane permeability to K+) to bring the membrane potential back to its resting potential near -70mV?_____________

When the membrane potential became more negative than the Threshold potential, the inactivated voltage-gated Na+ channels became reactivated. After the voltage-gated K+ channels closed to enable the membrane potential to return to resting membrane potential they became ready to open again. Both channels are ready to open again in order to fire another action potentia

sapphirepanda54

1a. all of the following are true about nerons except... (A. they produce ATP by cellular respiration, B. they are found in the central and peripheral nervous system, C. they have Na+/K+ pumps in their membranes, D. they can rapidly depolarize, E. they don't contain nucleir or mitochondria

1b. a reesting potential of -70mV ...(A. is possible because of voltage-gated sodium channels, B. is possible because of ligand-gated sodium, C. means that the outside of the neuron is more negative than the inside, D. is an IPSP that leads to threshold potential)

1c. after an action potential is triggered, the rapid increase in membrane potential to +50mV can be attributed to (A. opening of voltage-gated sodium channels, B. reversal of the direction of the sodium/potassium pump, C. opening of voltage-gated potassium, D. closing of ligand-gated potassium channels)

Tetraethylammonium (TEA) is a drug that blocks voltage-gated potassium channels. What effect would this have on an action potential?

(a)Prevent the rising phase

(b)Prevent the cell from reaching the threshold to trigger an action potential

(c)Prevent or prolong the falling phase

(d)None of the above

The hyperpolarization phase of the action potential is due to:

(a)The opening of voltage-gated Cl- channels

(b)Prolonged opening of voltage gated K+ channels

(c)The closure of resting Na+ channels

(d)Rapid inactivation of voltage-gated K+ channels

The period when it is difficult to initiate another action potential for several milliseconds due to voltage-gated sodium channel inactivation is referred to as the:

(a)Relative refractory period

(b)Absolute refractory period

(c)Resting period

(d)Hyperpolarization period

In the human central nervous system, Gap junctions are found:

(a)Only between neurons

(b)Only between astrocytes

(c)In both neurons and astrocytes

(d)In all cells

Small molecule transmitters such as acetylcholine are synthesized in:

(a)The nerve terminal

B) The cell body and transported to the nerve terminal

C) Synaptic vesicles

D) Endoplasmic reticulum

Prior to Otto Loewiâs classical experiment, which of the following was not known:

(a)stimulation of the vagus nerve slows the heart

(b)extracts of frog heart, made following vagal nerve stimulation, slow the heart

(c)some acetylcholine effects are similar to those produced by muscarine

(d)vagal nerve stimulation releases a substance which slows the heart

Which of the following is most important in determining if neurotransmission is excitatory or inhibitory?

(a)The structure of the synapse

(b)The neurotransmitter released by the presynaptic neuron

(c)The neurotransmitter receptor

(d)The strength of the stimulus

Benzodiazepines such as Valium allosterically regulate GABA receptors by:

(a)Binding at receptor sites other than the transmitter binding site

(b)Binding at the transmitter (GABA) binding site on the receptor

(c)Blocking the action of the endogenous transmitter

(d)Mimicking the action of the endogenous transmitter

GABA-A receptors are ligand-gated Cl- channels. The equilibrium potential of Cl- is -65 mV. At the neuronal resting membrane potential of -65 mV, GABA binding to the GABA-A receptor would result in the opening the Cl- channel, resulting in:

(a)no net flow of Cl- ions

(b)Cl- inflow and hyperpolarization

(c)Cl- outflow and depolarization

(d)Cl- outflow and hyperpolarization

At the mammalian neuromuscular junction, the released neurotransmitter acts on:

(a)muscarinic receptors

(b)nicotinic receptors

(c)adrenergic receptors

(d)Beta receptors

Neurotransmitters are packaged into synaptic vesicles by:

(a)endocytosis following transmitter release

(b)presynaptic membrane transporters

(c)vesicular transporters

(d)all of the above

. Which of the following are NOT types of ion channels?

Voltage-gated

(a)Ligand-gated

(b)G protein coupled receptor (GPCR)-gated

(c)Leak channels

(d)NONE of the above

NMDA receptors are unique in that their ion channel is:

(a)Ligand-gated

(b)Voltage-gated

(c)Ligand- and voltage-gated ion channels

(d)GPCR-gated

. Which of the following is INCORRECT regarding Catecholamine neurotransmitters

(a)Includes Dopamine, Norepinerphrine, and Epinephrine

(b)Contain a Catechol Ring

(c)Synthesized from Tryptophan

(d)Are produced by neurons whose cell bodies are located in the upper brainstem

The largest and most diverse group of receptors in eukaryotes is:

(a)Ligand gated receptors

(b)Glutamate receptors

(c)G-Protein coupled receptors

(d)Allosteric receptors

The most abundant G-protein coupled receptor in the brain is:

(a)Glutamate receptors

(b)Acetylcholine receptors

(c)Cannabinoid receptors

(d)Dopamine receptors

Which of the following drugs DOES NOT block voltage-gated Na+ channels

(a)Lidocaine

(b)Riluzole

(c)Reserpine

(d)Tetrodotoxin

Sarin, a nerve gas, exerts its toxicity by:

(a)blocking nicotinic receptors

(b)inhibiting choline acetyltransferase

(c)inhibiting acetylcholinesterase

(d)inhibiting voltage-gated Na+ channels

Botulinum Toxin (BoTox) interferes with transmitter release by:

(a)cleaving protein(s) involved in transmitter release

(b)blocking voltage-gated Ca2+ channels

(c)blocking voltage-gated Na+ channels

(d)blocking voltage-gated K+ channels

Atropine is:

(a)An agonist of the acetylcholine ionotropic receptor

(b)An antagonist of the acetylcholine ionotropic receptor

(c)An agonist of the acetylcholine metabotropic receptor

(d)An antagonist of the acetylcholine metabotropic receptor

CSB332H1 Lecture Notes - Lecture 8: Axon Hillock, Myelin, Voltage Clamp

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