Clozel M, Gray G A, Breu V, Löffler B M, Osterwalder R
Pharma Division, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Biochem Biophys Res Commun. 1992 Jul 31;186(2):867-73. doi: 10.1016/0006-291x(92)90826-7.
It has been suggested that the endothelin (ET) ETB receptor could mediate endothelium-dependent vasodilation to ET-1 or ET-3, but its in vivo role is still largely unknown. We used sarafotoxin S6C, a selective agonist of the ETB receptor, to study the in vivo effects of ETB stimulation. SRTX S6C induced a transient decrease in blood pressure, followed by a long-lasting pressor response accompanied by a marked renal and mesenteric vasoconstriction. No constriction was observed in isolated mesenteric arteries in vitro, indicating that the in vivo vasoconstrictor effect is most likely indirect. The pressor effect of SRTX S6C was not dependent on central stimulation of ETB receptors and was not mediated by catecholamines from the adrenal medulla, prostanoids or ET-1.
有人提出内皮素(ET)ETB受体可介导对ET - 1或ET - 3的内皮依赖性血管舒张作用,但其在体内的作用仍很大程度上未知。我们使用了ETB受体的选择性激动剂沙拉毒素S6C来研究刺激ETB的体内效应。沙拉毒素S6C引起血压短暂下降,随后是持久的升压反应,并伴有明显的肾和肠系膜血管收缩。在体外分离的肠系膜动脉中未观察到收缩,表明体内血管收缩作用很可能是间接的。沙拉毒素S6C的升压作用不依赖于ETB受体的中枢刺激,也不是由肾上腺髓质的儿茶酚胺、前列腺素或ET - 1介导的。