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ToxSci Advance Access originally published online on November 4, 2003
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Toxicological Sciences 78, 32-40 (2004)
Copyright © 2004 by the Society of Toxicology

HIGHLIGHTED ARTICLE

Human Interindividual Variation in Lymphocyte UDP-Glucuronosyltransferases as a Determinant of In Vitro Benzo[a]pyrene Covalent Binding and Cytotoxicity

Zhuohan Hu* and Peter G. Wells*,1,{dagger}

* Department of Pharmacology and {dagger} Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada M5S 2S2

1 To whom correspondence should be addressed at Faculty of Pharmacy, University of Toronto, 19 Russell St, Toronto, Ontario, Canada M5S 2S2. Fax: (416) 267-7797. E-mail: pg.wells{at}utoronto.ca.

ABSTRACT

UDP-glucuronosyltransterases (UGTs) catalyse the glucuronidation and elimination of most xenobiotics and, thereby, may prevent their alternative bioactivation to carcinogenic and teratogenic reactive intermediates. Previous studies have shown that glucuronidation, bioactivation, and covalent binding of the carcinogen/teratogen benzo[a]pyrene (BP) in rat lymphocytes accurately reflected those processes in hepatic microsomes from the same animals. Accordingly, lymphocytes from 12 normal human volunteers were incubated with BP metabolites to determine UGT variability and its potential toxicological relevance. Over 200-fold interindividual variability was observed in both the glucuronidation and covalent binding of BP metabolites, with decreasing total glucuronidation among subjects correlating with a decreased UGT-modulated reduction in covalent binding (R2 = 0.8272, p < 0.01) and, in six subjects, enhanced cytotoxicity (r = -0.9338, p < 0.001). Decreased glucuronidation of both BP diols (r = -0.9106, p < 0.001) and BP diones (r = -0.9625, p < 0.005), but not BP monophenols, correlated with enhanced cytotoxicity. These results provide the first evidence for substantial interindividual variability in UGT activities for BP metabolites among the normal population and suggest that UGT-deficient individuals may be at increased risk from the reactive intermediate-mediated effects of BP and related xenobiotics.

Key Words: glucuronidation; benzo[a]pyrene; cancer; birth defects; bioactivation; reactive intermediates.


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