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Drug Metab Rev. 2001 Aug-Nov;33(3-4):273-97.

The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism.

Author information

1
Department of Pharmacokinetics, Dynamics, and Metabolism, Pfizer Inc., PGRD, Groton, CT 06340, USA. michael_fisher@groton.pfizer.com

Abstract

At present, the methods and enzymology of the UDP-glucuronosyltransferases (UGTs) lag behind that of the cytochromes P450 (CYPs). About 15 human UGTs have been identified, and knowledge about their regulation, substrate selectivity, and tissue distribution has progressed recently. Alamethicin has been characterized as a treatment to remove the latency of microsomal glucuronidations. Most UGT isoforms appear to have a distinct hepatic and/or extrahepatic expression, resulting in significant expression in kidney, intestine, and steroid target tissues. The gastrointestinal tract possesses a complex expression pattern largely containing members of the UGT1A subfamily. Thus, these forms are poised to participate in the first pass metabolism of oral drugs. The authors and others have identified a significant expression of UGT1A1 in human small intestine, an enzyme possessing considerable allelic variability and a polymorphic expression pattern in intestine. Intestinal glucuronidation therefore plays a major role not only in first pass metabolism, but also in the degree of interindividual variation in overall oral bioavailability. Due to issues such as significant genetic variability and tissue localization in first-pass organs, clearance due to UGT1A1 should be minimized for new drugs.

PMID:
11768770
DOI:
10.1081/DMR-120000653
[Indexed for MEDLINE]

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