Vasopressin causes endothelium-dependent relaxations of the canine basilar artery

Z. S. Katusic, J. T. Shepherd, P. M. Vanhoutte

Research output: Contribution to journalArticle

207 Scopus citations

Abstract

The effect of synthetic 8-arginine vasopressin (vasopressin) was studied in isolated canine basilar, left circumflex coronary, and femoral arteries of the dog. Vascular rings with and without endothelium were suspended for isometric tension recording in physiological salt solution. The removal of the endothelium was confirmed by the absence of relaxations induced by either thrombin (basilar arteries) or acetylcholine (coronary and femoral arteries). In the basilar artery, vasopressin induced concentration-dependent inhibition of myogenic tone. In basilar and coronary arteries, the hormone caused concentration-dependent relaxations during contractions evoked by prostaglandin F(2α). In femoral arteries, vasopressin caused contraction. After removal of the endothelium, the inhibitory responses to vasopressin were abolished in basilar arteries and significantly reduced in left circumflex coronary arteries. The contractions of femoral arteries were not affected by endothelium removal. The V1-vasopressinergic antagonist d(CH2)5 Tyr (Me)AVP prevented the inhibitory response to vasopressin, but did not alter endothelium-dependent relaxations of basilar arteries caused by adenosine diphosphate. These results demonstrate that the endothelial cells mediate relaxation induced by vasopressin via specific V1-vasopressinergic receptors.

Original languageEnglish (US)
Pages (from-to)575-579
Number of pages5
JournalCirculation research
Volume55
Issue number5
DOIs
StatePublished - Jan 1 1984

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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