Filep J G, Hermán F, Battistini B, Chabrier P E, Braquet P, Sirois P
Department of Pathophysiology, Semmelweis University Medical School, Budapest, Hungary.
J Cardiovasc Pharmacol. 1991;17 Suppl 7:S216-8. doi: 10.1097/00005344-199100177-00062.
The effects of endothelin-1 (ET-1) on blood pressure and platelet aggregation were studied in anesthetized beagle dogs. Platelet aggregation was monitored in vivo by a filter-loop technique and in vitro by using platelet-rich plasma and whole blood. ET-1 (0.03-0.3 nmol/kg) induced a transient dose-dependent hypotension and inhibited platelet aggregation in vivo. These changes were accompanied by dose-dependent elevation of plasma 6-keto-PGF1 alpha levels. Pretreatment of animals with indomethacin (2 mg/kg plus 3 mg/kg/h) completely abolished the antiaggregatory action of ET-1 and significantly attenuated the hypotensive response to ET-1. Intra-arterial infusion of prostacyclin at concentrations similar to those observed following ET-1 injections mimicked the antiaggregatory and hypotensive actions of ET-1. ET-1 (0.1-100 nM) did not modify platelet aggregation induced by ADP, collagen, and platelet-activating factor in vitro, suggesting that dog platelets do not possess ET-1 receptors. These findings indicate that the antiaggregatory and hypotensive actions of ET-1 in beagle dogs are mediated through release of prostacyclin.
在麻醉的比格犬中研究了内皮素 -1(ET -1)对血压和血小板聚集的影响。通过滤环技术在体内监测血小板聚集,并在体外使用富含血小板的血浆和全血进行监测。ET -1(0.03 - 0.3 nmol/kg)可引起短暂的剂量依赖性低血压,并在体内抑制血小板聚集。这些变化伴随着血浆6 - 酮 - PGF1α水平的剂量依赖性升高。用吲哚美辛(2 mg/kg加3 mg/kg/h)预处理动物可完全消除ET -1的抗聚集作用,并显著减弱对ET -1的降压反应。以与ET -1注射后观察到的浓度相似的浓度进行动脉内输注前列环素,可模拟ET -1的抗聚集和降压作用。ET -1(0.1 - 100 nM)在体外并未改变由ADP、胶原和血小板活化因子诱导的血小板聚集,这表明犬血小板不具有ET -1受体。这些发现表明,ET -1在比格犬中的抗聚集和降压作用是通过前列环素的释放介导的。