Drug Disposition II Flashcards

2
Q

Drug metabolism results in: (3)

A

elimination/renal clearance blood levels effects

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3
Q

A member of the cytochrome P450 (CYP) enzyme superfamily High levels in the liver Metabolizes many drugs Genetic polymorphims results in humans with “normal” enzyme activity very low activity (no effect of codeine) very high activity

A

CYP 2D6 which is a gene

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4
Q

Key information needed to predict drug metabolism in your patient (3)

A

what enzymes metabolize genetic factors that affect enzyme drug activated or inactivated by metabolism

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5
Q

What are consequences of biotransformation? (2)

A

Increased polarity (water solubility), which results in facilitated excretion Pharmacological or toxicological result Inactivation (usually) Activation (sometimes) No effect Metabolite and parent drug may both be active

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6
Q

Sites of drug biotransformation (5):

A

Liver GI Kidney Respiratory tissues: lung, nose Brain, skin, heart

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7
Q

Common phases of drug metabolism: (2) Note: don’t necessarily have to go through both phases.

A

non-conjugative, (non-synthetic ) Oxidations Reductions, Hydrolyses Note: Adds or unmasks functional group Usually inactivates, sometimes activates conjugative (synthetic) Conjugations (covalent coupling of drug to endogenous molecule) Increases polarity Adds bulky moiety Usually inactivating

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8
Q

What is this? “microsomal” endoplasmic reticulum mixed-function oxidase uses NADPH and O2 to metabolize drugs

A

Cytochrome P450s

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9
Q

The major human cytochrome P450s involved in clinical drug metabolism: (4)

A

CYP 3 A 4 2 D 6 1 A 2 2 C

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10
Q

Conjugation (Phase II) reactions pathway involves: (2)

A

Need high-energy cosubstrate

  • Activities reduced when low ATP
  • Adds polar or ionizable group, increasing water solubility
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11
Q

In phase II reactions, what is the most common conjugation reaction? Has many enzymes and conjugates to many functional groups Are often excreted in the bile

A

glucuronides during glucuronidation

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12
Q

KNOW: Other conjugation reactions: (4) GASM

A

Acetylation Sulfation Methylation Glutathione conjugation

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13
Q

Which conjugation reaction’s main purpose is: to protect cells from reactive drugs and metabolites isnot usually a major pathway for drug elimination from the plasma

A

glutathione conjugation responsible for actetominophen poisoning for example

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14
Q

Factors affecting drug metabolism: (2)

A

Increased therapeutic/ toxic effect due to reduced metabolism neonates, liver disease, genetics, diet, herbal preparations Decreased therapeutic effect due to increased metabolism Gene amplification

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15
Q

P450 modifiers in natural products: (2)

A

grapefruit juice St. John’s Wort

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16
Q

In pharmacogenetics, genes can respond to drugs: (2)

A

monomorphic polymorphic (increased plasma concentration/magnitude of response)

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17
Q

Pharmacodynamic polymorphisms in drugs results in alterations in ______ molecules.

A

target

18
Q

This polymorphism; usually involves alterations in drug metabolizing enzymes more prevalent due to lower selection pressure

A

pharmacokinetic

19
Q

Detection of pharmacogenetic traits: (2)

A

Phenotyping Ex.Pharmacokinetics Urinary metabolite ratios Enzyme activities in peripheral blood Can detect all mutant alleles Affected genetic factors, can change with time Genotyping Easily done by sequencing or e.g. gene array chips Does not always reflect phenotype Only detects known mutant alleles

20
Q

Key themes/concepts in pharmacogenetics (2)

A

Multiple defective alleles/haplotypes Allele distribution can vary substantially in different racial/ethnic groups

21
Q

CYP2D6 polymorphism involves increased response to the following drug classes:

A

cardiovascular beta blockers tricyclic antidepressents

22
Q

10% of Caucasians 1% of Orientals Large number of mutant (defective) alleles

A

CYP2D6 polymorphism

23
Q

Pharmacodynamic polymorphisms in non-target genes is:

A

Malignant Hyperthermia