Pharmacodynamics Flashcards

1
Q

what the drug does to the body

A

pharmacodynamics

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2
Q

what the body does to the drug

A

pharmacokinetics

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3
Q

site of action of a drug

A

receptor

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4
Q

transmembrane proteins that open/close in response to changes in electrical potential difference across a cell membrane

A

voltage-gated ion channel

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5
Q

transmembrane proteins that open/close in response to the binding of a specific chemical messenger

A

ligand-gated ion channel

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6
Q

transmembrane proteins that act as both a receptor AND and ion channel; open in response to neurotransmitter binding

A

ionotropic receptors

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7
Q

cell surface receptors that trigger a cascade of events when they bind to a signal molecule… target for half of drugs (largest receptor family)

A

G-protein coupled receptors

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8
Q

concentration @ which 50% of the receptors are bound with ligand

A

Kd

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9
Q

how avidly a drug binds to its receptor

A

affinity

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10
Q

measure of activity.. or the effect of the drug on the body

A

Emax

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11
Q

maximal amount of ligand bound

A

Bmax

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12
Q

measure of potency.. conc of drug that induces a response halfway between the baseline and maximum after a certain amount of time

A

EC50

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13
Q

drug that binds its receptor and elicits a response that’s less than the maximal effect

A

partial agonists

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14
Q

measurement of EC50… the conc or amount of the drug required to produce the designed effect

A

potency

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15
Q

competes w/ a ligand for binding to the receptor… contributes to the equilibrium

A

competitive antagonist

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16
Q

binds to receptor w/ high affinity, but doesn’t dissociate… doesn’t contribute to the equilibrium

A

non-competitive antagonist

17
Q

attenuated response that occurs with sustained stimulation with a drug

18
Q

process by which the number of receptors is decreased

A

downregulation

19
Q

modifications of the receptor to minimize signaling

A

desensitization

20
Q

blocks the tonic activity of a receptor and reduces the basal activity

A

inverse agonist

21
Q

excess receptors beyond what can be used for signaling

A

spare receptors