Converting enzyme inhibitor ramipril stimulates prostacyclin synthesis by isolated rat aorta: evidence for a kinin-dependent mechanism

Klin Wochenschr. 1986 Aug 15;64(16):742-5. doi: 10.1007/BF01734341.

Abstract

The present study was performed to investigate the effect of the angiotensin I-converting enzyme inhibitor ramipril on vascular synthesis of prostacyclin (PGI2). Administration of ramipril (Hoe 498) to rats significantly stimulated prostacyclin (PGI2) synthesis, quantified by radioimmunoassay of its stable hydrolysis product 6-keto-PGF1 alpha, by portions of the animals' isolated aorta. This effect was maximal at a dose range of 10(-7) mol/kg ramipril. The addition of the active ramipril metabolite ramipril diacid directly into the incubation buffer at final concentrations of 10(-9), 10(-6), and 10(-4) M resulted in a dose-dependent stimulation of 6-keto-PGF1 alpha released by isolated aortic tissue. Pretreatment of rats with aprotinin (40,000 U s.c. 60 min before the incubations) attenuated the ramipril-induced effect on aortic 6-keto-PGF1 alpha synthesis. Our results show that the angiotensin I-converting enzyme inhibitor ramipril stimulates PGI2 synthesis in vascular tissue and that this effect may be secondary to changes in the activity of the kinin system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / metabolism
  • Angiotensin-Converting Enzyme Inhibitors*
  • Animals
  • Aorta, Abdominal / drug effects
  • Bridged Bicyclo Compounds / pharmacology*
  • Bridged-Ring Compounds / pharmacology*
  • Dose-Response Relationship, Drug
  • Epoprostenol / biosynthesis*
  • Female
  • Kinins / metabolism*
  • Muscle, Smooth, Vascular / drug effects*
  • Muscle, Smooth, Vascular / metabolism
  • Ramipril
  • Rats
  • Rats, Inbred Strains
  • Stimulation, Chemical

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Bridged Bicyclo Compounds
  • Bridged-Ring Compounds
  • Kinins
  • 6-Ketoprostaglandin F1 alpha
  • Epoprostenol
  • Ramipril