Role of endothelium in the contractile response of rat aorta to α-adrenoceptor agonists

Author:

Godfraind ThéOphile1,Egleme Cécile1,Osachie Iyad Al1

Affiliation:

1. Laboratoire de Pharmacodynamie Générale et de Pharmacologie, Université Catholique de Louvain, Bruxelles, Belgium

Abstract

1. The influence of endothelium on the response of rat isolated aorta to α-adrenergic agonists has been studied by comparing the response of intact and denuded preparations before and after treatment with calcium entry blockers flunarizine and nifedipine. 2. Endothelium removal enhanced the response of the preparations, especially to α2-agonists that had a weak effect in intact preparations. In the absence of endothelium, about 80% of the maximum response to clonidine was blocked by calcium entry blockers, whereas only 25% of the maximum response to noradrenaline was sensitive to them. In contrast about 40% of maximum noradrenaline-evoked contractions was sensitive to calcium entry blockers in the presence of endothelium. This may be attributed to an increase in the intracellular exchangeable calcium fraction, likely to be due to a slight depolarization of smooth muscle membrane of denuded preparations, which are highly sensitive to the calcium agonist BAY K 8644. 3. The results indicate that a factor liberated by endothelial cells controls both calcium entry and calcium release evoked by α-adrenoceptor agonists in vascular smooth muscle.

Publisher

Portland Press Ltd.

Subject

Ocean Engineering

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