Antibiotic furazolidone induces CYP1A but not CYP2E1 subfamily in rat liver

J Vet Med Sci. 2008 Mar;70(3):223-6. doi: 10.1292/jvms.70.223.

Abstract

Furazolidone (FZ), one of the nitrofuran fungicides, is used as a veterinary medicine in the Middle and Far Eastern countries. In this study, FZ (125 mg/kg) was administered orally to Wistar rats for 3 days. Results of the Ames test using the S-9 fraction of rats treated with FZ showed a significant increase in the number of revertant colonies. Western blot analysis of hepatic CYP isozymes induced by FZ, revealed a remarkable induction of CYP1A1 apoprotein, but CYP1A2 and CYP2E1 apoproteins were not altered. In addition, the expression of CYP1A1 mRNA level in rats treated with FZ by RT-PCR was significantly enhanced by FZ treatment. We concluded that FZ is apparently mutagenic and induces transcription of the CYP1A1 isozyme, which metabolically activates numerous promutagens, in hepatocytes.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Blotting, Western
  • Cytochrome P-450 CYP1A1 / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Furazolidone / pharmacology*
  • Gene Expression Regulation / drug effects*
  • Isoenzymes / metabolism
  • Liver / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Anti-Bacterial Agents
  • Isoenzymes
  • Furazolidone
  • Cytochrome P-450 CYP1A1