3- Pharmacodynamics Flashcards

1
Q

additive vs. synergistic

A

drug A = 20 drug B = 20

A+ B = 40 = additive
A+B = 90 = synergistic

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2
Q

estrogen receptor

vitamin A/retinoic acid receptor

A

intracellular receptors

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3
Q

bind lipophillic agents

A

intracellular receptors

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4
Q

consequence of ligand binding is a change in gene activity(transcription)

A

often an intracellular receptor

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5
Q

single membrane spaning domain with extracelullar ligand binding area and intracellular enzymatic activity area

A

intrinsic enzymatic activity receptor

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6
Q

tyrosine kinases

A

receptor with intrinsic enzymatic activity

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7
Q

epidermal growth factor receptor
insulin receptor
transforming growth factor receptor

A

receptors with intrinsic enzymatic activity

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8
Q

leptin receptor
erythropoietin
interleukin-3

A

receptors that directly associate with intracellular enzymes

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9
Q

nAchR

A

ligand-gated ion channel

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10
Q
rhodopsin
frizzled
odorant receptors
smoothened receptors
beta adrenergic receptors
A

7MSR aka serpentine or heptahelical receptors

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11
Q

can 7MSR mediate signals that are independent of gprtn signaling

A

yes

can mediate signals that require coupling to a g prtn OR are independent of gprtn signaling

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12
Q

downregulation

A

continued stimulation of a receptor leads to a decreased number of receptors

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13
Q

upregulation

A

continued exposure of a receptor to an inhibitor causes a increase in number of receptors

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14
Q

decreased physiological response to the same amount of drug

A

tolerance

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15
Q

increased physiological response to the same amount of drug

A

sensitization

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16
Q

equation for dissociation constant Kd

A

kd = (concentration of drug x concentration of ligand) / concentration of receptor bound drug

17
Q

point at which half the receptors are occupied with ligand and half the receptors are free

A

Kd dissociation constant

18
Q

higher affinity = ____________ Kd

A

lower Kd

the lower the Kd (or less drug required for half maximal occupancy), the greater the binding affinity of that drug

19
Q

concentration of drug that produces a half-maximal response

A

EC50

20
Q

comparing the EC50 of drugs tells you …

A

potency

21
Q

comparing the Emax of drugs tells you …

A

efficacy

22
Q

a drug that binds to a receptor and produces a response

A

agonist

23
Q

a drug or ligand that binds to a receptor and inhibits the response produced by the agonist

A

antagonist

24
Q

compete for the same binding site

A

competitive antagonist

25
Q

bind to different sites

A

noncompetitive antagonist

26
Q

induces a shift to the right in EC50 of dose curve but max effect is still achievable

A

competitive antagonist

max effect is still achievable because the antagonist can be outcompeted with higher concentrations of agonist but the EC50 of the agonist is increased

27
Q

decrease in the maximal effect of the agonist without changing the binding affinity (EC 50 doesn’t change)

A

noncompetitive antagonist

28
Q

drug that produces a lower maximal response compared to the agonist

A

partial agonist

29
Q

overall result of increasing partial agonists =

A

blunted overall physiological response (see graphs)

30
Q

dose at which 50% of individuals exhibit a specific quantal effect

A

ED50

31
Q

dose at which 50% of individuals exhibit a toxic effect

A

TD50

32
Q

dose at which 50% of individuals die

A

LD50

33
Q

therapeutic index ID =

A

TD50 / ED50

34
Q

a higher ID = ______________ safety

A

increased safety

more wiggle room between lethal and therapeutic doses