Pharmocology Flashcards

1
Q

What are the target molecules for drugs?

A

ion channels, receptors, enzymes, transporters

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2
Q

what are the intracellular responses that can happen with drug binding?

A

G-protein binding, binding to nucleus receptors altering gene transcription, opening of ligand gated ion channels, binding to kinases linked receptors

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3
Q

Competitive reversible antagonish

A

an antagonist can compete with an agonist for the same target molecule

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4
Q

Competitive irreversible antagonism

A

when a competitive antagonist binds irreversibly to the target molecule

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5
Q

non-competitive antagonists

A

do not compete with agonists for the same target molecule but prevent the events set in motion by the agonist binding that lead to a response.

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6
Q

physiological antagonism

A

an agonist may inhibit the actions of another agonist by having the opposite effect

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7
Q

Pharmacokinetic antagonism

A

one drug affects the absorption, distribution, metabolism, or elimination of another in a manner that reduces its actions

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8
Q

chemical antagonism

A

one drug interacts with another in solution leading to a reduction or loss of activity

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9
Q

tolerance

A

a term typically used to describe a more gradual decrease in responsiveness to a drug

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10
Q

resistance

A

a term typically used to describe the loss of effectiveness of antimicrobial or anti-cancer drugs

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11
Q

Tachyphylaxis

A

densensitisation

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12
Q

Inverse agonist

A

drugs which bind to such receptors and reduce the response

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13
Q

Which graph is used to measure the efficacy and potency?

A

dose response curve

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14
Q

why is a drug given by a particular route

A

the properties of the drug, and the therapeutic objective

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15
Q

Properities of the drug that affect the drug absorption from site of adminisitration

A

lipid solubility, molecular weight, and chemical properties (ionisation)

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16
Q

physiological factors of drug that affect the drug absorption from site of adminisitration

A

local blood flow, surface area of the abosrbing surface

17
Q

Where can the drugs distribute throughout the body after adminsitration

A

plasma, interstitial fluid, intracellular fluid, transcellular fluid, site of administration

18
Q

Why is VD important

A

enables you to predict whether the drug selected for administration is likely to reach the target site at effective concentrations

VD can be used to determine the loading dose necessary to achieve a target plasma concentration

19
Q

How can drugs accumulate in tissues (tissue trapping)

A

high lipid solubility- this leads to accumulation in fat
ion trapping due to differences in pH across barriers
binding to a site within a tissue or cell