Cell membrane Flashcards

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0
Q

Forces that drive diffusion

A

osmotic pressure, partial pressures, concentration, charge

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1
Q

Reflection Coeff.

A

1=impermeable, 0= totally permeable

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2
Q

tonicity

A

indicates effect of osmolarity of a solution on cell volume

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3
Q

hypertonic solution

A

causes contracted cell volume

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4
Q

hypotonic solution

A

causes expansion of cell volume

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5
Q

normal plasma osmolarity

A

280 mOsmol/L water

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6
Q

3 types of gated channels

A

ligand, ion, stretch

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7
Q

3 types of carrier-mediated transport

A

facilitated diffusion, coupled carrier transport (secondary active, co- & counter), active transport

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8
Q

example of ion channel mechanism important for cardiac muscle contraction?

A

Ca-Na exchanger allows Na influx which triggers Ca-dependent Ca release from SR in cardiac cell -> contraction

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9
Q

Hyperkalemia

A

high potassium=acidosis

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10
Q

the 4 mechanisms of transport

A

channel (passive), active transport, coupled carrier, facilitated diffusion (gated)

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11
Q

example of facilitated diffusion

A

GLUT-4 transporter for glucose: it must bind glucose outside the cell before it opens (but only if conc. gradient drives!)

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12
Q

What ion is commonly used to drive coupled carrier counter-transporters?

A

Na+

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13
Q

How does one tell a facilitated diffusion transporter from a coupled carrier transporter?

A

the coupled carrier transporter will reach a saturation maximum rate (flux)

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14
Q

3 characteristics of binding specificity in receptors

A

their ligands may be agonists/antagonists, they may bind more than one ligand, they are differentially expressed in individuals

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15
Q

first messenger

A

extracellular signal

-fat or water-soluble classifications

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16
Q

Kd

A

the ligand concentration where 50% of all receptors are bound.
higher Kd= lower receptor affinity for that ligand

17
Q

what determines effectiveness of competitive inhibition

A

ligand concentration

18
Q

competitive inhibitors act to…

A

reduce or increase (competitive excitation) the response of a ligand

19
Q

are competitive inhibitors more or less potent drugs

A

they are less potent than non-competitive inhibitors- because they disallow the original binding partner from interacting with the receptor regardless of the ligand concentration increase by the body

20
Q

describe equilibrium potential of a membrane

A

the net movement of ions is zero. If the gradient is bidirectional, the number of ions moving by concentration gradient equals the number moving by electrical/ voltage gradient

21
Q

Nernst potential meaning

A

the equilibrium potential of a certain ion; what the resting potential would be if only that ion existed; based on outside over inside concentration of CATIONS

22
Q

which 3 ions most significantly affect the resting membrane potential

A

Na, K, Cl

23
Q

Goldman-Hodgkin-Katz (GHK) Equation

A

predicts the resting membrane potential (based on relative permeability * outside/inside concentration for CATIONS, reverse for anions)

24
Q

Why is the resting membrane potential closer to that of K than Na

A

because the membrane is significantly more permeable to K (3 K in, 2 Na out via ATPase, and leak K channels)

25
Q

Why should we never worry about our membrane potential getting disrupted

A

because ATPase is in excess in all cells of the body

26
Q

what are the two ways by which the membrane capacitor does work

A

graded potentials and action potentials

27
Q

why does Na channel opening lead to depolarizations

A

because ENa (equilib potential) is more positive than Vm (voltage potential)

28
Q

Steady state potentials vs. equilibrium potentials

A

steady state pot.-when the current through the membrane is 0, the voltage is the constant (resting membrane potential)
equilibrium pot. -the electrical potential that balances concentration gradient energy

29
Q

what does it mean that graded potentials are conducted DECREMENTALLY

A

the degree of polarization is dependent on how close one takes the potential measurement relative to the stimulus site

30
Q

in what type of inhibitor can the ligand concentration overcome the inhibition

A

competitive

31
Q

do inhibitors affect affinity of a ligand for its receptor

A

yes

32
Q

what type of inhibitor binds at a site other than the ligand-binding site

A

non-competitive inhibitor

33
Q

two cellular locations for steroid hormone receptors

A

cytoplasm, intra-nuclear

34
Q

the 4 mechanisms for receiving water-soluble first messengers

A

ion channels, tyrosine kinase, g-protein, janus kinase

35
Q

JAK kinase examples

A

cytokines (interleukins, interferons)

36
Q

adenylyl cyclase cascade

A

effector plasma membrane receptor downstream of a G-protein-coupled receptor. response requires [Ca ++ ] intracellular via intracellular release or IP3, activates PKA
(ex: beta-adrenergic receptor for ephinephrine)

37
Q

IP3 cascade

A

G-protein-coupled receptor activates phospholipase C, makes IP3, activates PKC with diacylglycerol (DAG), Ca++ ER release

38
Q

absolute refractory potential

A

The time it takes for the action potential to exclude a subsequent action potential - no matter the stimulus strength

39
Q

relative refractory period

A

about 2 times the absolute refractory period (~0- -10 V) can elicit another action potential if stimulus is great enough. Outward K must be overcome by inward Na of new stimulus.