The metabolism of 4,8-DiMeIQx in conventional and germ-free rats

Carcinogenesis. 1989 Aug;10(8):1479-84. doi: 10.1093/carcin/10.8.1479.

Abstract

The aromatic amine mutagen, [14C]2-amino-3,4-8-trimethyl-imidazo[4,5-f]quinoxaline (4,8-DiMeIQx), which is derived from cooked food, was administered to conventional and germ-free AGUS rats previously fed either a semi-synthetic diet containing the cytochrome P-450 inducer beta-naphthoflavone (BNF) or a control diet without BNF. The germ-free animals had longer fecal transit times and lower induction of 7-ethoxyresorufin-O-deethylase activity than conventional rats. Induction with BNF caused a greater percentage of the radioactivity to be excreted in the feces of both germ-free and conventional rats. Feeding BNF also caused a 4-fold induction in germ-free and a 24-fold induction in conventional rat intestinal enzyme levels. Analysis of the urinary and fecal metabolites showed no consistent differences between conventional and germ-free rats in the metabolite profile. Major metabolites were identified as 8-hydroxymethyl-DiMeIQx, N-acetyl-8-hydroxymethyl-DiMeIQx, and 3-N-dimethyl-4-hydroxy-methyl-DiMeIQx. The data from this study indicate that intestinal microflora do not play a major role in the metabolism of 4,8-DiMeIQx, but the induction of intestinal enzymes does not affect the route and rate of excretion.

Publication types

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

MeSH terms

  • Animals
  • Carbon Radioisotopes
  • Chromatography, High Pressure Liquid
  • Germ-Free Life
  • Male
  • Mutagenicity Tests
  • Mutagens / metabolism*
  • Quinoxalines / metabolism*
  • Quinoxalines / pharmacokinetics
  • Quinoxalines / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Salmonella typhimurium / drug effects

Substances

  • Carbon Radioisotopes
  • Mutagens
  • Quinoxalines
  • 3,4,8-trimethylimidazo(4,5-f)quinoxalin-2-amine