Aflatoxin B1-induced 8-hydroxydeoxyguanosine formation in rat hepatic DNA

Carcinogenesis. 1995 Feb;16(2):419-22. doi: 10.1093/carcin/16.2.419.

Abstract

A time- and dose-dependent increase in 8-hydroxydeoxyguanosine (8-OHdG) was observed in rat hepatic DNA after a single i.p. injection of aflatoxin B1 (AFB1). It was also found that pre-treatment with selenium or deferoxamine significantly reduced 8-OHdG level in AFB1-administered rats. In contrast, no reduction in 8-OHdG concentration was found in vitamin E-pre-treated rats. These results provide evidence that AFB1 causes oxidative DNA damage in rat liver, which may involve hydroxyl radicals as the initiating species. It is postulated that AFB1-induced oxidative DNA damage (8-OHdG formation) may constitute an important pathway in AFB1 hepatocarcinogenesis.

Publication types

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

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Aflatoxin B1 / toxicity*
  • Animals
  • DNA / drug effects*
  • DNA / metabolism*
  • DNA Damage*
  • Deferoxamine / pharmacology
  • Deoxyguanosine / analogs & derivatives*
  • Deoxyguanosine / biosynthesis
  • Liver / drug effects*
  • Liver / metabolism*
  • Male
  • Oxidation-Reduction
  • Rats
  • Rats, Inbred F344

Substances

  • 8-Hydroxy-2'-Deoxyguanosine
  • DNA
  • Aflatoxin B1
  • Deoxyguanosine
  • Deferoxamine