Term
enzymes and transporter proteins |
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Definition
responsible for normal metabolism
significant role in drug absorption in the GI tract and portal system (Ff and Fg) |
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Term
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Definition
oxidase that converts endogenous and exogenous (drugs) substrates into more excretable molecules
super family of enzymes
in liver, GI, kidney, pancreas
responsible for phase I metabolism of >50% of medications |
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Term
cyp450 enzyme family includes |
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Definition
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Term
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Definition
primary subfamily enzyme in humans
in liver, GI, kidney, pancreas |
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Term
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Definition
liver: 30% jejunum: 70% high variable concentrations between people: 10 - 100 fold diff in liver and 30 fold diff in intestine |
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Term
P-glycoprotein (PGP) transporters |
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Definition
plasma membrane glycoprotein belonging to an ATP-binding cassette (ABC) transporter superfamily
energy dependent drug efflux pump
promotes excretion of medications into bile, GI tract, or urine
limits transport of drugs across BBB |
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Term
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Definition
liver, small intestine, kidney, panacrease, brain, spleen, lung, adrenal gland, testes |
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Term
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Definition
its possible since cyp and pgp share substrates, location in tissues, and location in epithelial cells of tissue |
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Term
cyp3a and pgp concentrated in? |
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Definition
in many tissues including the intestines and liver |
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Term
cyp3a enzymes _______ drug intestinal absorption by _______ drugs before the can be absorbed into the ______. |
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Definition
decrease metabolizing portal circulation |
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Term
pgps _______ intestinal absorption by ______ drugs from the intracellular space back into the ______ |
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Definition
decrease pumping intestinal lumen |
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Term
_______ bioavailability of drugs that are substrates for cyp enzymes and pgps |
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Definition
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Term
first-pass metabolism (first-pass loss) Fh |
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Definition
drug absorbed from GI into portal circulation
metabolized by the liver
fraction of drug does not reach systemic absorption |
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Term
the liver metabolizes some drugs thus _____ delivered to the ______ |
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Definition
decreasing the amount systemic circulation Fh |
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