Cardiovascular control 1 Flashcards

1
Q

what happens to the membrane potential when there is an impermeable membrane

A

2 different conc KCl on differnt sides

device measures chemical concentration? - chem conc gradient - no potential difference because no movement of ions

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2
Q

what happens to the membrane potential when the membrane is selectively permeable to K

A

no cl movement - no membrane potential
K move down conc gradient and take +ve charge - charge builds up so repels K ions
conc grad balanced by electrical gradient at equilibrium
no net movement of ions
this is the membrane potential

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3
Q

what is the driving force

A

the difference between concentration and electrical gradient

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4
Q

what happens, looking at K, to driving force when membrane is open to K

A

it is 0 at equilibrium

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5
Q

describe the resting membrane potential

A

depends on flow of K
predict in ideal situations - Nerst eqn
if only permeable to K, potential across it will equal Ek
solve nerst eqn for K

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6
Q

action of the Na/K ATPase

A

pump k out, Na in - against conc gradients
needs ATP to drive
doesn’t contribute to mem potentialmaintains conc gradient

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7
Q

why does teh RMP change

A

depends on relative permeabilities of the ions

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8
Q

EK and Ena

A

-80

+66mV

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9
Q

when is the mem potential similar to Ena

A

when mem selectively permeable to Na

during upstroke

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10
Q

what does the Goldman-Hodgkin-katz equation do

A

take into consideration the relative permeability to the membrane at a particular time

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11
Q

length of nerve AP

A

2ms

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12
Q

what happens in a nerve AP

A

if threshold is reached upstroke is fired because of a large opening of Na channels and so increase of permeability, big conc grad so na enter cell depolarising it
towards Ena
not quite Ena - channels close quickly more K channel open - k out of cell
repolarise

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13
Q

compare teh cardiac AP to the nervous AP

A

longer, 200-300ms - allows control of strength of heart beat
long slow contraction = efficient pumping

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14
Q

cardiac refractory period

A

Na channel inactivation
more repolarised the cell gets , ie more -ve, smaller stimulus needed
more channels recovered and can be activated
longer than in skeletal muscle - not possible to rexcite until full contraction, muscle is electrically inert
allow heart to fill before next contraction - not possible to be tetanised

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15
Q

when is refractory period in skeletal muscle

A

early in contraction phase

re stimulation and summation possible

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16
Q

phases of the ventricle AP

A
phase 0 - upstroke 
1 - early repolarisation 
2 - plateau 
3 - repolarisation 
4 - RMP, diastole period
17
Q

describe upstroke

A
increase in Pna
Na channels open 
influx of Na 
depolarisation 
poteential towards Ena
18
Q

describe the early repolarisation

A

small
opening of channel give rise to transient outward current Pto
this is carried by K ions
brief opening and closing of channels
cause efflux of K ions out of the cell to repolarise

19
Q

what happens simultaneously to Pto

A

increase Pca
ca important for Ca induced ca release - important for contraction
rapid increase in opening of channels
ca current updates rapidly but upstroke caused by Pna
Ca channels still open during platau - don’t change quickly