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Current Drug Metabolism

Editor-in-Chief

ISSN (Print): 1389-2002
ISSN (Online): 1875-5453

Accelerated Cytotoxicity Mechanism Screening Using Drug Metabolising Enzyme Modulators

Author(s): P. J. O'Brien and A. G. Siraki

Volume 6, Issue 2, 2005

Page: [101 - 109] Pages: 9

DOI: 10.2174/1389200053586082

Price: $65

Abstract

By assessing how drug/new chemical entity (NCE) cytotoxicity is affected when their metabolic pathways are inhibited or activated, the metabolic pathways that activate versus detoxify drugs/NCEs can be identified. Reactive metabolites contributing to cytotoxicity can also be identified. In the following, the drug metabolizing enzyme inhibitors and activators used in vitro with freshly isolated rat hepatocytes for the accelerated cytotoxicity mechanism screening (ACMS) of drugs/NCEs (a technique used in our laboratory) are reviewed and, this technique is useful for determining in vivo rat hepatotoxicity mechanisms. The enzyme inhibitors/activators have been chosen on the basis of their selectivity, modulator effectiveness, and their lack of toxicity. The use of these inhibitors/activators with human hepatocytes or subcellular fractions for assessing human hepatotoxicity mechanisms is also reviewed.

Keywords: cytochrome p-450, hepatotoxicity, glucuronosyltransferase, arylamine n-acetyltransferase, sulfotransferases, glutathione transferase, coenzyme a-transferases, enzyme Inhibitors

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