Preparation, isolation, analysis, and characterization of 3-benzo[a]pyrenyl-beta-D-glucopyranosiduronic acid: a metabolite of 3-hydroxybenzo[a]pyrene with potentially high carcinogenic activity

Anal Biochem. 1978 Nov;91(1):138-45. doi: 10.1016/0003-2697(78)90824-2.

Abstract

The aglycone, 3-hydroxybenzo[a]pyrene, was metabolized to 3-benzo[a]pyrenyl-beta-D-glucopyranosiduronic acid in the presence of uridine 5'-diphosphoglucuronic acid and rabbit liver microsomes. The course of the biosynthetic reaction was followed by fluorimetry and reverse-phase, paired-ion high pressure liquid chromatography (HPLC). Also, the HPLC system was used to analyze for glucuronide and 3-hydroxybenzo[a]pyrene during the isolation procedure. The existence of a glucuronide of 3-hydroxybenzo[a]pyrene was determined by radiotracer and enzymic techniques, utilizing the HPLC system. Field desorption and direct inlet mass spectral techniques were used to characterize the 3-hydroxybenzo[a]pyrene glucuronide.

Publication types

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

MeSH terms

  • Animals
  • Benzopyrenes / analysis
  • Benzopyrenes / isolation & purification*
  • Benzopyrenes / metabolism
  • Carcinogens / analysis
  • Carcinogens / isolation & purification*
  • Carcinogens / metabolism
  • Chromatography, High Pressure Liquid / methods
  • In Vitro Techniques
  • Mass Spectrometry
  • Microsomes, Liver / metabolism
  • Rabbits
  • Spectrometry, Fluorescence

Substances

  • Benzopyrenes
  • Carcinogens
  • benzo(a)pyrene-3-O-glucuronide
  • 3-hydroxybenzo(a)pyrene