Pharmacodynamics Flashcards

1
Q

Describe the basic drug-receptor theory

A

Agonist drug binds to receptor = Activation = Response

Measure response via organ bath simulation at contraction/relaxation of tissue

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2
Q

Define affinity (KD)

A

Tendency for ligand to form stable complex with receptor

Governed by bonds and shape of ligand

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3
Q

Define an agonist and its two components

A

A drug that binds to receptors to produce a response

  1. Binds to occupy a receptor (Affinity)
  2. Produces a response (efficacy)
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4
Q

Define Bmax

A

Maximum number of binding sites, Measures saturation

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5
Q

Define Dissociated constant, Kd (M)

A

Affinity of binding (how well drug binds to receptor)

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6
Q

Is a higher or lower Kd better and why?

A

Lower Kd = Means it has highest affinity to fully bind at lowest conc

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7
Q

Define an antagonist

A

The drug that binds to a receptor without mediating a response but blocks agonist response

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8
Q

What are the 5 types of antagonism?

A

Competitive antagonism (reversible/irreversible) receptor effector block (non-comp), chemical, pharmacokinetic, physiological antagonism

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9
Q

Describe non competitive antagonism

A

Blocks receptor activation and response, doesn’t compete for receptor site

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10
Q

Describe chemical antagonism and an example

A

2 substances combine in solution, effect of active drug is lost
Eg chelating agents that bind to heavy metals reduce toxicity

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