MCELLBI C61 Lecture Notes - Lecture 7: Axon Hillock, Multiple Sclerosis, Sodium-Potassium Alloy

12 views2 pages

goldgnat162

21 Mar 2020

School

Berkeley

Department

Molecular And Cell Biology

Course

MCELLBI C61

Professor

David Presti

For unlimited access to Class Notes, a Class+ subscription is required.

Document Summary

Semipermeable barrier: contains channels that selectively allow particles through. Outside of neuron: more na(+), more cl(-), more ca(++), k(+) Inside of neuron: na(+), cl(-), ca(++), more k(+) Hyperpolarization: opening of k channel makes a more negative inside. Depolarization: opening of na channel makes a more negative inside. Starts at axon hillock + ends at the synapses. Voltage gated na channels close > voltage peaks. Propagation of action potential/nerve impulse along an axon. Prevents the action potential from traveling both ways. It takes a millisecond for the neuron to settle into a resting state where it"s able to produce another action potential. Energy source: atp, which carries energy within cells. 3 na out / 2 k in > 1 atp used. Nerve signal propagation along axon: 10 m/s, 20 mph. Louis antoine ranvier: axons are coated with myelin, separated by nodes of ranvier. ~100 in unmyelinated axon ~>10000 in myelenated axon. Myelin speeds nerve impulse propagation via saltatory condition.

Related Questions

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

6. Consider the presence of hemoglobin in the catheter bag. Whatsymptom would this loss of

hemoglobin most strongly and immediately be linked to in thepatient?

A. Loss of blood volume

B. Loss of heartbeat

C. Drop in blood oxygen saturation

D. Liver failure

When a neuron is stimulated, the area of the membrane at thepoint of stimulation becomes

more permeable to Na+. If a cell starts at resting potential(-70mv), and is then stimulated:

A. The membrane voltage will become < -70mV, because Na+will move OUT of the cell.

B. The membrane voltage will become > -70mV, because Na+will move OUT of the cell.

C. The membrane voltage will become < -70mV because Na+will move INTO the cell.

D. The membrane voltage will become > -70mV because Na+will move INTO the cell.

. At the peak of the action potential, the Na+ voltage-gatedchannels close, and K+ voltage-gated

channels open in response to the positive membrane potential.In order to return the cell to its

negative resting potential quickly:

A. K+ will diffuse along its concentration gradient INTO thecell.

B. K+ will diffuse along its concentration gradient OUT of thecell.

C. Na+ will reverse its direction of diffusion OUT of thecell.

D. The sodium-potassium pump will move Na+ OUT of the cell andK+ INTO the cell.

E. None of the above would return the cell to its negativeresting potential quickly.

You experiment with higher concentrations of toxin and findcases when the cell could not

repolarize at all or, if it began to repolarize, itimmediately depolarized again. This tells you that

the toxin:

A. Prevents voltage-gated K+ channels from opening.

B. Increases the speed that the Na+ ion channels open.

C. Prevents the Na+ ion channels from closing.

D. Makes the Na+ ion channels close too soon.

E. Doesn

lavenderclam549

Santiago Ramon y Cajalâs theory of dynamic polarization refers to the:

(a)membrane potential of a neuron at rest.

(b)membrane potential of a neuron firing action potentials.

(c)opening and closing of gated channels in the membrane.

(d)one way flow of information in neurons from dendrites to axon terminals.

(e)one way flow of information in neurons from axon terminals to dendrites.

Over the course of scientific history, there are many examples of scientists reaching the right conclusion for the wrong reasons. When Schwann first proposed that the nervous system was made of individual cells, he based it on observations of:

(a)synapses.

(b)dendrites

(c)axon terminals.

(d)astrocytes.

(e)Nodes of Ranvier.

The synaptic cleft was finally seen in the 1950s. What prevented scientists from seeing it earlier?

(a)The resolution of the light microscope.

(b)They were looking in the wrong place.

(c)Their tissue was not appropriately stained.

(d)Myelination of the axons.

(e)all of the above

The resting membrane potential of a neuron is approximately:

(a) +65 V

(b) +65 mV

(d) -65 mV

What is largely responsible for the resting membrane potential in a neuron?

(a)Axonal insulation by myelin

(b)Voltage-Gated Sodium Channels

(c)The Action Potential

(d)Potassium Leak Channels

Which of the following would DECREASE the propagation velocity of an action potential down an axon?

(a)Increase in axon diameter

(b)Increase myelination between nodes of Ranvier

(c)Remove myelination between nodes of Ranvier

(d)Decrease density of voltage-gated Na+ channels except at the Nodes of Ranvier

The resting membrane potential of a neuron can be estimated using the:

(a)Nernst equation

(b)Goldman equation

(c)Hodgkin and Huxley equation

(d)Ohmâs law

18. What would happen to the resting membrane potential of a neuron if you added K+ to the extracellular fluid?

(a)Resting membrane potential would increase (become more positive)

(b)Resting membrane potential would decrease (become more negative)

(c)Resting membrane potential would not change

(d)Resting membrane potential would be abolished

. Which of the following statements is FALSE for Graded Potentials

(a)Magnitude changes with magnitude of triggering stimulus

(b)Magnitude decreases with distance from initial site

(c)Cannot be summed

(d)No refractory period

In the nervous system, the strength of the stimulus is coded into:

(a)The frequency of action potentials generated

(b)The amplitude of action potentials generated

(c)Both the frequency and amplitude of action potentials generated

(d)The duration of individual action potentials generated

Ion movement during both the depolarization and repolarization phases of an action potential are the result of:

(a)active transport pumps along the neuron membrane.

(b)diffusion of ions down their electrochemical concentration gradients.

(c)negative feedback loops.

(d)All of the above

At the peak of the action potential, the membrane potential is:

(a)Exactly at the Na+ equilibrium potential

(b)Greater (more positive) than the Na+ equilibrium potential

(c)Above 0 mV but less positive than the Na+ equilibrium potential

(d)0 mV

MCELLBI C61 Lecture Notes - Lecture 7: Axon Hillock, Multiple Sclerosis, Sodium-Potassium Alloy

Document Summary

Get access

Related Documents

MCELLBI C61 Chapter Notes - Chapter 5: Neuroglia, Oligodendrocyte, Axon Hillock

MCELLBI C61 Lecture Notes - Lecture 8: Otto Loewi, Dendritic Spine, Axon Terminal

PSYC 251 Lecture Notes - Lecture 1: Electric Potential, Turing Test, Peripheral Nervous System

Related Questions