BIOL 220 Study Guide - Midterm Guide: Pacemaker Potential, Sinoatrial Node, Membrane Potential

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ochreporcupine180

4 Nov 2016

School

Department

Biology

Course

BIOL 220

Professor

Doherty Jennifer

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Na + ions flow into pacemaker cell via funny na+ channels. Na+ positive charge causes cell to depolarize and reach threshold. Voltage-gates ca2+ channels open in response to depolarization to threshold and depolarize the cell more. K+ ions flow out of the cell, causing it to hyperpolarize. Signal from sa node propagates to cardiac muscles via gap junctions. Voltage-gated na+ channels open in response to depolarization and allow na+ ions to move into the cell. Voltage-gates na+ channels close and voltage-gated k+ channels open. K+ ions move out of the cell, slightly hyperpolarizing the cell. Voltage-gated ca2+ channels open and ca2+ ions move into the cell. Voltage-gated k+ channels remain open, hyperpolarizing the cell to a membrane potential close to but not at ek. Signal from sa node reaches cardiac muscles via gap junctions. Voltage-gated na+ channels open and allow na+ ions to move into the cell. Voltage-gated k+ channels open and slightly hyperpolarize cell.

Related Questions

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

40. When a protein is synthesized within the cell, this process represents a chemical reaction that is:

		explosive
		exergonic and anabolic
		exergonic and catabolic
		endergonic and anabolic
		endergonic and catabolic

39. Chemical bonds in carbohydrates (i.e., glucose) and fats, have:

		no potential or kinetic energy
		large amount of kinetic energy
		large amount of potential energy
		small amount of potential energy
		small amount of kinetic energy

38. When Na+ moves into the cell following the openning of Na+ channels, _____________________________.

		the ion charge across the membrane in the area that Na+ moves in will change.
		voltage-gated channels will close.
		an action potential will be observed.
		the cell will hyperpolarize.
		same amount of K+ ions will move out of the cell to counteract the Na+ moving into the cell.

blacklion206

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

BIOL 220 Study Guide - Midterm Guide: Pacemaker Potential, Sinoatrial Node, Membrane Potential

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