Exam 2: Ch5 Book Since Exam 1 Flashcards

1
Q

every cell that is in a nonexcited or “resting” state has…

A

a potential difference (Vrest) across the membrane

usually lies between -20 and -100 mC depending on the kind of cell and ionic envionment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

2 factors govern resting potential

A

presence of open selective ion channels

unequal extracellular and intracellular distribution of ions maintained by active transport (allows membrane potential)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

ions influence the ________ across a membrane roughly in proportion to the _______ of the membrane to each ion species

A

potential, permeability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

if a membrane is only permeable to one ion, will the distribution of that ion dictate the membrane potential?

A

yes, use Nernst equation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Vrest in frog skeletal muscle

A

-90 to -100

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

resting potential depends on which ions

A

Mostly K and some Na

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

resting potentials of muscle, nerve, and other cells are more sensitive to changes in [ ]… than the concentrations of other _____

A

[K] out, cations

consistent finding with high permeability of plasma membranes to K, compared to other cations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

why do large changes in [Na] out have ______ effect on Vrest

A

little

b/c resting membrane is relatively impermeable to Na

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

how to calculate force acting on an ion

A

emf(x) = Vm - E(x)

depends on how different membrane potential is from equilibrium potential

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

based on [ ] gradient, there is a steady influx of which ion into the cell if not maintained by active transport?

A

Na, large electric driving force (extra: 120mM; intra: 10mM)

would accumulate inside cells if not removed, depolarizing the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

if Na were allowed to leak in at rest, what would happen to K

A

it would leak out b/c internal negatively less able to hold K in

K high intracell, low extracell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

which pump contributes to Vrest and how

A

Na/K pump (3 Na out / 2K in)

indirectly maintains high internal [K]

directly (very small effect) moves net pos charge out of cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

if you inhibit Na/K pump…

A

concentration gradients diminished

Na goes in, K eventually goes out and no Vrest b/c equilibrium will be reached

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is an action potential

A

a large, brief change in Vm that is propagated along an axon without decrement

all or none

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

3 key elements to producing an AP

A

active transport of ions to maintain [ ] gradients

[ ] gradient generates an electrochemical gradient that provides a reservoir of potential energy

electrochemical gradient drives ions across membrane when selective channels open (changes Vm)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what two voltage-gated ion channels are responsible for all the features of the AP

A

voltage gated Na and K

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

APs are generated by the membranes of ….

A

neurons

muscle cells

receptor cells, secretory cells, and some single-celled animals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

local response

A

when a depolarization stimulus brings the membrane almost to threshold, there is an abortive, non-propagated excitation

beginning of an AP that died out before it reached threshold

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

threshold current

A

intensity of depolarizing stimulus that is just sufficient to bring membrane to threshold and elicit an AP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

most neurons have threshold currents between…

A

-30 and -50 mV

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

what does regenerative mean

A

self-perpetuating AP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

overshoot

A

brief period when interior of membrane is positive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

after-hyperpolarization

A

transient period when Vm is more negative than Vrest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

refractory

A

for a short time after an AP, it is difficult or impossible to trigger another AP

absolute refractory period

relative refractory period

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

absolute refractory period

A

if 2nd stimulus is delivered during an AP or immediately after, no AP is triggered

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

relative refractory period

A

slightly after the absolute refractory period, if stim is delivered an AP may be triggered but stim must be stronger than usual

amplitude of AP may be smaller (breaks all or none rule)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

threshold potential decreases during the _____ refractory period until the membrane returns to its normal resting state

A

relative

28
Q

what happens when a neuron is stimulated with a series of subthreshold depolarization

A

excitability progressively decreases

the stronger the series of subthreshold currents, the stronger they actually need to be to reach threshold

29
Q

accommodation

A

the phenomena that the slower the rate of increase in the intensity of the stimulating current, the greater the increase in threshold potential

caused by time-dependent changes in the way membrane channels respond to depol

30
Q

can some neurons accommodate rapidly?

A

yes

some generate 1-2 APs (phasic response)

some fire repeatedly but with decreasing frequency (tonic response)

31
Q

adaptaion

A

the decrease in frequency of APs seen in a neuron that responds tonically during sustained stimulus

visualized as increasing distance between APs

32
Q

what causes the rapid depolarization of an AP

A

inward Na current caused by a sharp increase in Na conductance (rising phase)

opening of voltage-gated Na channels

33
Q

when voltage-gated Na channels close and permeability of Na drops (peak of AP), what happens to K

A

memb. much more permeable to K b/c voltage-gated K channels are still open

falling phase

34
Q

why do animals have giant axons

A

rapid conduction of AP

escape response

35
Q

what did Hodgkin and Huxley discover about resistance and capacitance

A

membrane resistance during an AP decreases, but capacitance remains constant

therefore, change in conductance is entirely responsible for change in ionic current

36
Q

what did Hodgkin and Huxley discover about voltage during AP

A

goes past 0 toward ENa of nernst equation (58 mV in squid giant axon)

when Na removed (artificial seawater), magnitude of AP decreased as more Na removed

37
Q

why use a squid giant axon (1mm in diameter)

A

thin electrode wires could be threaded longitudinally

38
Q

equation for current carried by ionic species

A

I(x) = g(x)*(Vm-E(x))

I(x) = current carried by ionic species x

g(x) = membrane conductance for X (proportional to # of open channels selective for x)

V(m) = membrane potential

E(x) = equilibrium potential of x

39
Q

what does equation for current carried by ionic species demonstrate

A

there is only an ionic current across the memb. if there is a force driving the movement of ion x, and a conductance for x

if g(x) or emf acting on X is -0, there is no I(x)

40
Q

what does it mean if g(x) is 0

A

no channels are open

41
Q

changes in ionic ________ play a major role in controlling the electric currents carried across biological membranes

A

conductance

42
Q

4 pieces of evidence that Na is the major ionic species responsible for AP

A

[Na] out exceeds [Na] by ~10, ENa ~55-60 mV so emf acting on Na is large and drives Na into cell

entry of pos charged Na produced pos shift in Vm

overshoot of AP approaches ENa

magnitude of overshoot changes as a function of [Na] out (artificial seawater)

43
Q

voltage clamping

A

method used on giant squid axon allows you to change the Vm abruptly to any value, and hold it there

can therefore measure ionic current flowing across memb.

Ohms law to calculate conductance

44
Q

when Hodgkin and Huxley abruptly depolarized an axonal memb. from its resting level they were able to measure…

A

initial transient inward current of Na to drive rising phase followed by a sustained outward current of K for falling phase

45
Q

voltage clamping method

A

electronic feedback system holds voltage difference across plasma membrane at a constant

electrode inserted into neuron and control amplifier compares potential across membrane

use solutions of different ion [ ] or agents that block particular ion channels

46
Q

tetrodotoxin (TTX) pufferfish fugu

A

blocks voltage-gated Na channels (know from radiolabel)

47
Q

are there many voltage gated sodium channels in cell memb

A

no, makes up small surface area

however, 10^7 Na ions or more per second can pass through

48
Q

unitary current

A

current through a single channel

49
Q

which technique elucidated how voltage gated Na channels operate

A

patch-clamping

50
Q

gating current

A

I(g)

small measurable current associated in time with opening and closing of Na channels

51
Q

mechanism of voltage gated Na channels

A

gating takes place with movement of charges

activation and inactivation are coupled processes

52
Q

selectivity of channels

A

determine relative permeability to each ion

channel filters partly by size, net charge, and ease of dehydration

selectivity filter: part of channel that determines selectivity

53
Q

positive feedback loop during AP (Hodgkin’s cycle)

A

Na channels respond to depol but opening, allowing Na to enter cell, which depol it more

this extra depol causes more channels to open, allowing even more Na to enter causing an explosive regenerative event

once AP started it needs no more stimulus to continue

54
Q

limits of Hodgkin’s cycle

A

as membrane potential approaches ENa, driving force on Na is reduce so less is driven into the cell

open Na channels become inactivated after a short time even if depol is maintained

55
Q

how are Na channels opened

A

activation gate closed and inactivating particle located away from channel

when voltage clamped to depol, activation gate opens and inward current is maxed when most Na channels are open

as depol continues, inactivating particle blocks channels

after membrane repolarization, inactivation particle unblocks channels and activation gate closes (memb. must be inside-negative)

56
Q

what is patch-clamping

A

variation of voltage clamping that allows currents through a single membrane channel to be recorded

57
Q

do voltage gated K channels respond to changes more quickly or slowly than Na channels

A

slowly

58
Q

when does membrane conductance of K change in an AP

A

only near its peak (very slow rise before then)

remains elevated during falling phase

59
Q

during after-hyperpolarization, membrane potential moves even closer to ___

A

E(K) equilibrium potential of K

60
Q

are voltage gated K channels needed to generate APs?

A

no

61
Q

benefit of rapid membrane repolarization produced by current through K channels

A

shortens AP, but allows neurons to generate them with higher frequency

62
Q

how do glial cells help maintain Vrest

A

remove K from extracellular fluid surrounding axons

slowly release it allowing it to be reclaimed by neurons

63
Q

lidocaine blocks

A

Na channels

dentists use for pain… no signals conducting

64
Q

K channel structure

A

each gene codes for a subunit (4) monomeric alpha arranged around a central pore

4 beta subunits associated with each channel modulate function

65
Q

Na channel structure

A

1 large alpha protein with 4 same transmembrane domains

central pore

66
Q

Ca channels

A

help depol w/ inward current a little

open more slowly and conduct less current

67
Q

Ca can act as a

A

intracellular messenger