Renal and hepatic microsomal enzymes responsible for bioactivation of 3-methoxy-4-aminoazobenzene in the rodent

Biochem Pharmacol. 1991 Oct 9;42(9):1655-9. doi: 10.1016/0006-2952(91)90499-u.

Abstract

Activities of the renal and hepatic microsomal enzymes responsible for the N-hydroxylation and mutagenic activation of 3-methoxy-4-aminoazobenzene (3-MeO-AAB) were examined in male mice, rats, hamsters and guinea pigs. In all these rodent species, hepatic microsomes showed definite N-hydroxylation of 3-MeO-AAB, whereas the renal activity was detected only in mice. The hepatic enzyme responsible for N-hydroxylation of 3-MeO-AAB (3-MeO-AAB N-hydroxylase) was induced in all species except mice by phenobarbital and selectively in mice and hamsters by 3-methylcholanthrene, whereas these cytochrome P450 inducers did not affect the renal enzyme in mice, rats or hamsters. In individual microsome samples, activities for N-hydroxylation and mutagenic activation of 3-MeO-AAB correlated well. These results indicate that the renal and hepatic enzymes responsible for the metabolic activation of 3-MeO-AAB differed among different species of rodent animals in terms of their activity and inducibility with cytochrome P450 inducers.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biotransformation
  • Cricetinae
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Enzyme Induction
  • Guinea Pigs
  • Hydroxylation
  • Kidney / drug effects
  • Kidney / enzymology*
  • Male
  • Mesocricetus
  • Methylcholanthrene / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology*
  • Mutagenicity Tests
  • Phenobarbital / pharmacology
  • Rats
  • Rats, Inbred F344
  • p-Aminoazobenzene / analogs & derivatives*
  • p-Aminoazobenzene / metabolism

Substances

  • Methylcholanthrene
  • p-Aminoazobenzene
  • 3-methoxy-4-aminoazobenzene
  • Cytochrome P-450 Enzyme System
  • Phenobarbital