WHERE DO DRUG BIOTRANSFORMATIONS
OCCUR?
Although
every tissue has some ability to metabolize drugs, the liver is the principal
organ of drug metabolism. Other tissues that display considerable activity
include the gastrointestinal tract, the lungs, the skin, the kidneys, and the
brain. After oral administra-tion, many drugs (eg, isoproterenol, meperidine,
pentazocine,
Some orally administered drugs (eg, clonazepam, chlorpromazine, cyclosporine)
are more extensively metabolized in the intestine than in the liver, while
others (eg, midazolam) undergo significant (≈ 50%) intestinal metabolism. Thus, intesti-nal
metabolism can contribute to the overall first-pass effect, and individuals
with compromised liver function may rely increasingly on such intestinal
metabolism for drug elimination. Compromise of intestinal metabolism of certain
drugs (eg, felodipine, cyclosporine A) can also result in significant elevation
of their plasma levels and clinically relevant drug-drug interactions (DDIs, ).
First-pass effects may so greatly limit the bioavailability of orally administered
drugs (eg, lidocaine) that alternative routes of administration must be used to
achieve therapeutically effective blood levels. Furthermore, the lower gut
harbors intestinal micro-organisms that are capable of many biotransformation
reactions. In addition, drugs may be metabolized by gastric acid (eg,
peni-cillin), by digestive enzymes (eg, polypeptides such as insulin), or by
enzymes in the wall of the intestine (eg, sympathomimetic catecholamines).
Although
drug biotransformation in vivo can occur by sponta-neous, noncatalyzed chemical
reactions, most transformations are catalyzed by specific cellular enzymes. At
the subcellular level, these enzymes may be located in the endoplasmic
reticulum (ER), mitochondria, cytosol, lysosomes, or even the nuclear envelope
or plasma membrane.
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