Peroxidatic oxidation of benzo[a]pyrene and prostaglandin biosynthesis

Biochemistry. 1979 Jul 10;18(14):2923-9. doi: 10.1021/bi00581a001.

Abstract

The arachidonic acid dependent oxidation of benzo[a]pyrene to a mixture of 3,6-, 1,6-, and 6,12-quinones has been studied by using enzyme preparations from sheep seminal vesicles. Maximal oxidation is observed at 100 microM benzo[a]pyrene and 150 microM arachidonic acid. The arachidonic acid dependent oxidation is peroxidatic and utilizes prostaglandin G2 (PGG2), generated in situ from arachidonate, as the hydroperoxide substrate. 15-Hydroperoxy-5,8,11,13-eicosatetraenoic acid is equivalent to PGG2 as a hydroperoxide substrate, but hydrogen peroxide, cumene hydroperoxide, and tert-butyl hydroperoxide are much poorer substrates. Arachidonic acid dependent benzo[a]pyrene oxidation by microsomal and solubilized enzyme preparations is markedly.

Publication types

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

MeSH terms

  • Animals
  • Benzopyrenes / metabolism*
  • Heme / metabolism
  • In Vitro Techniques
  • Male
  • Methemoglobin / metabolism
  • Microsomes / enzymology
  • Microsomes, Liver / metabolism
  • Oxidation-Reduction
  • Peroxides / metabolism*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Prostaglandins / biosynthesis*
  • RNA, Transfer / metabolism
  • Rats
  • Seminal Vesicles / ultrastructure
  • Sheep

Substances

  • Benzopyrenes
  • Peroxides
  • Prostaglandins
  • Heme
  • Methemoglobin
  • RNA, Transfer
  • Prostaglandin-Endoperoxide Synthases