Stimulation of prostacyclin production by vitamin C in ram seminal vesicle microsomes: possible mode of action

Arch Int Pharmacodyn Ther. 1985 Sep;277(1):56-65.

Abstract

The enhancing effect of vitamin C on the conversion of arachidonic acid, endoperoxide G2 and endoperoxide H2 to 6-keto-PGF 1 alpha, the stable metabolite of prostacyclin, by ram seminal vesicle microsomes was further investigated. From the incubations of these substrates with 1-tryptophan, catalase, superoxide dismutase and 15-HPETE it became clear that vitamin C apparently acts mainly through neutralization of the oxidative species formed during the reduction of endoperoxide G2 to endoperoxide H2. Although it has also a more direct stimulating activity on the prostacyclin synthase, a possible interference with hydroperoxy derivatives of arachidonic acid cannot be completely ruled out.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acids / pharmacology
  • Ascorbic Acid / pharmacology*
  • Catalase / pharmacology
  • Epoprostenol / biosynthesis*
  • Epoprostenol / pharmacology
  • In Vitro Techniques
  • Leukotrienes*
  • Lipid Peroxides / pharmacology
  • Male
  • Microsomes / metabolism*
  • Prostaglandin Endoperoxides, Synthetic / metabolism
  • Prostaglandin H2
  • Prostaglandins G / metabolism
  • Prostaglandins H / metabolism
  • Seminal Vesicles / metabolism*
  • Sheep
  • Superoxide Dismutase / pharmacology
  • Tryptophan / pharmacology

Substances

  • Arachidonic Acids
  • Leukotrienes
  • Lipid Peroxides
  • Prostaglandin Endoperoxides, Synthetic
  • Prostaglandins G
  • Prostaglandins H
  • Prostaglandin H2
  • prostaglandin G2
  • 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid
  • Tryptophan
  • Epoprostenol
  • Catalase
  • Superoxide Dismutase
  • Ascorbic Acid