Vasodilator responses to nitric oxide are enhanced in mesenteric arteries of portal hypertensive rats

Eur J Clin Invest. 1996 Sep;26(9):824-6. doi: 10.1046/j.1365-2362.1996.2340557.x.

Abstract

Nitric oxide (NO) is discussed as a mediator of the splanchnic hyperaemia in portal hypertension. We assessed the vasorelaxation by the NO-dependent vasodilator acetylcholine, the NO donor 3-morpholino-sydnonimine (SIN-1) and forskolin, a stimulator of the adenylate cyclase pathway in potassium-preconstricted isolated perfused mesenteric arteries of portal vein-ligated and sham-operated rats. Dilator responses to acetylcholine and SIN-1 were significantly enhanced in vessels of portal vein-ligated rats as compared to sham-operated rats, whereas no difference was found in forskolin-induced vasodilatation. This suggests enhanced reactivity of the vasculature to NO in experimental portal hypertension.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Dose-Response Relationship, Drug
  • Hypertension, Portal / physiopathology*
  • Male
  • Mesenteric Arteries / drug effects*
  • Molsidomine / analogs & derivatives
  • Molsidomine / pharmacology
  • Nitric Oxide / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Vasodilation / drug effects*
  • Vasodilator Agents / pharmacology

Substances

  • Vasodilator Agents
  • Nitric Oxide
  • linsidomine
  • Molsidomine
  • Acetylcholine