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Drug Metabolism and Disposition Fast Forward
First published on December 8, 2005; DOI: 10.1124/dmd.105.007435


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Received for publication September 20, 2005.
Revised December 1, 2005.
Accepted for publication December 2, 2005.

Expression of UDP-Glucuronosyltransferase Isoform mRNAs During Inflammation and Infection in Mouse Liver and Kidney

Terrilyn A Richardson 1, Melanie Sherman 1, Daniel Kalman 1, Edward T Morgan 1*

1 Emory University

* Address correspondence to: E-mail: etmorga{at}emory.edu

Abstract

Inflammation or infection down-regulate the activity and expression of cytochrome P450 (P450) enzymes involved in hepatic drug clearance, possibly altering drug effectiveness and leading to toxicity. The regulation of UDP-glucuronosyltransferases (UGTs) in inflammation and infection is less well characterized. To determine the response of hepatic and renal UGTs during inflammation and infection, mice were administered either saline or 1 mg/kg LPS (16 hours), or Citrobacter rodentium by oral gavage (6 days). Hepatic mRNA expression of UGT1A1, 1A9, and 2B5 were similarly down-regulated after LPS exposure and C. rodentium infection, whereas UGT1A2 and 1A6 mRNAs were unchanged. Effects of C. rodentium infection did not require a functional Toll-like receptor 4 (TLR4). Conversely, renal UGT isoforms were relatively unaffected, except for UGT2B5 induction after LPS treatment. Regulation of UGTs during the inflammatory response exhibits similarities and differences with regulation of P450s, and may be cytokine-mediated.


Key words: cytokines, gene regulation, glucuronidation, UDP glucuronyltransferases





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