Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 34, Issue 11, Pages 1435-1446Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/S0891-5849(03)00151-5
Keywords
valproic acid; 15-F-2t-isoprostane; cytochrome P450; oxidative stress; lipid peroxidation; free radicals
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The mechanism by which valproic acid (VPA) induces liver injury remains unknown, but it is hypothesized to involve the generation of toxic metabolites and/or reactive oxygen species. This study's objectives were to determine the effect of VPA on plasma and hepatic levels of the F-2-isoprostane, 15-F-2t-IsoP, a marker for oxidative stress, and to investigate the influence of cytochrome P450- (P450-) mediated VPA biotransformation on 15-F-2t-IsoP levels in rats. In rats treated with VPA (500 mg/kg), plasma 15-F-2t-IsoP was increased 2.5-fold at t(max) = 0.5 h. Phenobarbital pretreatment (80 mg/kg/d for 4 d) in VPA-treated rats increased plasma and liver levels of free 15-F2t-IsoP by 5-fold and 3-fold, respectively, when compared to control groups. This was accompanied by an elevation in plasma and liver levels of P450-mediated VPA metabolites. Pretreatment with SKF-525A (80 mg/kg) or 1-aminobenzotriazole (100 mg/kg), which inhibited P450-mediated VPA metabolism, did not attenuate the increased levels of plasma 15-F-2t-IsoP in VPA-treated groups. Plasma and hepatic levels of 15-F-2t-IsoP were further elevated after 14 d of VPA treatment compared to single-dose treatment. Our data indicate that VPA increases plasma and hepatic levels of 15-F-2t-IsoP and this effect can be enhanced by phenobarbital by a mechanism not involving P450-catalyzed VPA biotransformation. (C) 2003 Elsevier Inc.
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