3. Pharmacodynamics, Drug Interaction, and Toxicology Flashcards

1
Q

What are the conventional mechanisms of action of drugs?

A

Interactions with endogenous proteins - cell surface receptors, nuclear receptors, enzymes, ion channels, transporters, signal transduction proteins etc.

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2
Q

What is the unconventional mechanism of action that vinca alkaloids and colchicine utilise?

A

Disruption of structural proteins

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3
Q

What is the unconventional mechanism of action that streptokinase utilises?

A

Being enzymes

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4
Q

What is the unconventional mechanism of action that cyclophosphamide utilises?

A

Covalently linking to macromolecules

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5
Q

What is the unconventional mechanism of action that antacids utilise?

A

Reacting chemically with small molecules

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6
Q

What is the unconventional mechanism of action that infliximab and drugs for heavy metal poisoning utilise?

A

Binding to free molecules/atoms

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7
Q

What is the ideal standard for a drug?

A

Acts at one site (selective) and performs one certain action (specific). This isn’t realistic, real drugs have side effects.

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8
Q

Give an example of drug selectivity

A

Penicillin targets an enzyme involved in bacterial cell wall synthesis, but not human cell wall synthesis.

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9
Q

Give an example of drug specificity

A

Adrenergic receptors - Beta 1 in heart, Beta 2 in lungs

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10
Q

What is affinity?

A

Drug tendency to bind to specific receptor types

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11
Q

What is efficacy?

A

Ability of drug to produce a response as a result of receptors being occupied

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12
Q

What is potency?

A

Dose required to produce the desired biological response

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13
Q

What is the therapeutic index?

A

The relationship between concentrations of a drug causing overdose and concentrations causing the desired effect.

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14
Q

Is a higher or lower therapeutic index better?

A

Higher as that means there is a larger margin of safety.

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15
Q

What is the therapeutic window?

A

The range of doses that can be used to treat a pt with a specific drug while remaining safe

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16
Q

Name some drugs with a narrow therapeutic window.

A

Warfarin
Digoxin
Aminophylline
Aminoglycoside abx

17
Q

When drugs interact, at what levels can they interact?

A

Absorption
Distribution/Protein binding
Metabolism

18
Q

What can be altered to affect GI absorption of a drug?

A

P-glycoprotein activity (active transporter)

19
Q

Which drugs is protein binding interactions most relevant for?

A

IV drugs
Drugs with a short haf life
Drugs with a narrow therapeutic window

20
Q

What classes of drugs are the usual suspects for drug interactions?

A
Anticonvulsants
Antibiotics
Anticoagulants
Antidepressants/psychotics
Antiarrhythmics
21
Q

What other “DDI” is important to remember?

A

Drug Disease interactions

22
Q

What diseases should we look out for when thinking about drug interactions?

A

Renal, kidney, and liver disease

23
Q

Why is renal disease important in drug metabolism?

A

If cleared by kidneys or affect functioning of the kidneys (nephrotoxic), renal disease decreases GFR so clearance is decreased, so can predispose to toxicity.

24
Q

What is the classic example of drug interactions in hepatic disease?

A

Opiates in cirrhosis -> accumulation of small doses -> coma. Reduced clearance so drug half life increases.

25
Q

Why is cardiac disease important wrt drug interactions?

A

Reduced CO -> reduced organ perfusion, and an increased response to hypotensive aagents

26
Q

What does grapefruit juice interact with, and how?

A

Inhibits CYP450 isoenzymes affecting simvastatin, amiodarone, and terfenadine among others.

27
Q

What does cranberry juice interact with, and how?

A

Inhibits CYP2C9 isoform -» warfarin, anticoagulants. High risk of haemorrhage.