NADPH-dependent oxidation of benzidine by rat liver

Vijaya M. Lakshmi, Nathan T. Zenser, F. F. Hsu, Michael B. Mattammal, Terry V. Zenser, Bernard B. Davis

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


This study used liver microsomes from control and β-naphthoflavone-treated rats to evaluate NADPH-dependent oxidation of benzidine. With microsomes from β-naphthoflavone-treated rats, the rates of formation of aqueous soluble metabolite (HPLC analysis) and protein and DNA binding were 835 ± 81, 14.5 ± 1.8 and 0.71 ± 0.14 pmol/ mg/min respectively. β-Naphthoflavone treatment elicited 12.3-, 1.8- and 14.2-fold increases in benzidine metabolism compared with controls as judged by HPLC and protein and DNA binding respectively. For microsomes from treated animals, K(m) and V(max) values were 47 ± 6 μM and 1.13 ± 0.14 nmol/mg protein/min respectively. All of the metabolic parameters were inhibited to varying degrees by glutathione (1 or 10 mM), N-acetylmethionine (10 mM) and ascorbic acid (10 mM). Following glutathione addition, at least two new metabolite peaks were observed, representing ~6% of the total radioactivity recovered by HPLC. Neither metabolite was 3-(glutathion-S-yl)benzidine. Cytochrome P450 inhibitors (10 μM) specific for different members of cytochrome gene families 1-3 indicated that benzidine was metabolized by cytochrome P450 1A1/1A2. Ellipticine and α-naphthoflavone, specific 1A1/1A2 inhibitors, elicited 50% inhibition at ~0.2 and 0.5 μM respectively. Electron impact and negative ion chemical ionization mass spectrometry identified the aqueous soluble metabolite as 3-hydroxybenzidine. The lability of 3-hydroxybenzidine observed at pH > 7.0 was prevented by ascorbic acid. Thus, cytochrome P450 1A1/1A2 NADPH-dependent metabolism of benzidine to 3-hydroxybenzidine was demonstrated.

Original languageEnglish
Pages (from-to)1941-1947
Number of pages7
Issue number9
StatePublished - Sep 1996


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