Biological reactive intermediates of bisfuranoid mycotoxins

J Toxicol Sci. 1990 Dec:15 Suppl 4:152-8. doi: 10.2131/jts.15.supplementiv_152.

Abstract

Based on the mode of action of AFB1 and the activities of its biologically active intermediates, one may conclude that: 1. The mode of toxic action of the bisfuranoid mycotoxin is through epoxidation of the vinyl ether double bond of their dihydrobisfuran functionality. 2. The DNA and plasma albumin adducts formed in vivo may be useful in the molecular dosimetry of these environmental carcinogens. 3. Monitoring of these adducts of AFB1 in biological samples so far indicates that aflatoxin is likely involved in the etiology of human liver cancer.

Publication types

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

MeSH terms

  • Aflatoxin B1
  • Aflatoxin M1
  • Aflatoxins / chemistry
  • Aflatoxins / metabolism
  • Aflatoxins / toxicity*
  • Animals
  • Anthraquinones / chemistry
  • Anthraquinones / metabolism
  • Anthraquinones / toxicity*
  • DNA / drug effects
  • DNA / metabolism
  • Humans
  • Liver Neoplasms / chemically induced
  • Mice
  • Mutagenesis
  • Mycotoxins / chemistry
  • Mycotoxins / metabolism
  • Mycotoxins / toxicity*
  • Rats
  • Serum Albumin / drug effects
  • Serum Albumin / metabolism
  • Sterigmatocystin / analogs & derivatives
  • Sterigmatocystin / chemistry
  • Sterigmatocystin / metabolism
  • Sterigmatocystin / toxicity*

Substances

  • Aflatoxins
  • Anthraquinones
  • Mycotoxins
  • Serum Albumin
  • Sterigmatocystin
  • O-methylsterigmatocystin
  • Aflatoxin M1
  • DNA
  • Aflatoxin B1
  • versicolorin A