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When a neurotransmitter opens a ligand-gated channel to an unknown ion+ and nochange in the membrane potential of –60 mV is observed, then the unknown ion+(assume that [K+]out=12 mM, [K+]in=120 mM, [Na+]out=140 mM, and [Na+]in=14 mM):

a. has a greater electrical than chemical potential

b. has a net outward flux

c. is at equilibrium

d. is in equal concentrations in and outside the nerve

e. is at a greater concentration outside the nerve than inside the nerve

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Bunny GreenfelderLv2
28 Sep 2019
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Related questions

For a cell with 120 mM K+, protein- inside, and 4 mM K+ outside, with proteins-impermeable and K+ permeable to the membrane, which of the following statements istrue at equilibrium?a. The chemical potential driving K+ inward is equal in magnitude to the electricalpotential driving potassium outward.

b. Bulk movement of K+ out of the cell occurs due to the impermeable proteins-.

c. The net flux of potassium equals zero.

d. There will be 62 mM K+ protein inside and 62 mM K+ protein outside the cell.

e. The inside of this cell will be electrically positive with respect to the outside.

1. The plasma membrane of rod and cone cells are

a) At resting potential in the dark and deploarized in thelight

b) At resting pootential in the dark and hyperpolarized in thelight

c) Depolarized in the dark and hyperpolarized in the light

d) Hyperpolarized in the dark and at resting potential in thelight

e) Hyperpolarized in the dark and depolarized in the light

2. The equilibrium potential of K+ ions in nerve cells is about-90mV. The membrane potential of a typical nerve cells at rist is-70mV. Therfore

a) Increasing the permeability of a resting neuronal membrane toK+ ions will increase the membrane potential (that is, make it morenegative, inside with respcect to outside)

b) In nerve cells at rest, there is a net diffusion of K+ ionsout of the cell

c) Increasing the membrane potential of a nerve cell would slowthe diffusion of K+ ions out of it.

d) K+ is not the only ion that is permeable at rest

e) All of the above

3. Which of the following is responsible for the replarizingphase of the action potential?

a) Voltage-gated Na+ channels are opened.

b) The Na+-K+ pump restores the ions to theri original restingstate.

c) The permeability to Na+ increases greatly.

d) ATPase destroys the energy supply that was maintaining theaction potential at its peak.

e) The permeability to K+ increases greatly while that to Na+decreases

4. The Relative refractory period of an axonm conincides withthe period of

a) Activation and inactivatioin of voltage-gated Na+channels

b) Increased Na+ flux into the cell

c) Increased K+ flux into the cell

d) Increased K+ flux out of the cell

e) Increased Na+ flux out of the cell

5. The plasma membranes of rod and cone cells are

a) At resting potential in the dark and epolarized in thelight

b) At resting potential in the dark and hyperpolarized in thelight

c) Depolarized in the dark and hyperoplarized in the light

d) Hyperpolarized in the dark and tat resing potential in thelight

e) Hyperpolarized in the dark and depolarized in the light

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 Loewi’s 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

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