Jamieson M J, Shepherd A M, Jackson S H, Patel S S, Flanagan P H, Galbraith H
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7764.
Res Commun Chem Pathol Pharmacol. 1988 Nov;62(2):173-85.
Urapidil is a new antihypertensive vasodilator agent whose pharmacologic action in man has not yet been fully defined. We have assessed the alpha adrenergic blocking activity of urapidil 15 and 30 mg given intravenously in a single blind study in 8 healthy volunteers. Urapidil produced dose-dependent parallel shift of the phenylephrine log dose/blood pressure response curve, consistent with significant competitive peripheral alpha 1 antagonism. Mean dose ratios were 2.99 and 5.48 for the 15 mg and 30 mg doses respectively. The pA2 for alpha 1 blockade is 7.3. Given these data, the major mechanism of antihypertensive effect of urapidil may be alpha 1 antagonism in the peripheral vasculature.
乌拉地尔是一种新型抗高血压血管扩张剂,其在人体中的药理作用尚未完全明确。我们在一项针对8名健康志愿者的单盲研究中,评估了静脉注射15毫克和30毫克乌拉地尔的α肾上腺素能阻断活性。乌拉地尔使去氧肾上腺素对数剂量/血压反应曲线产生剂量依赖性平行移位,这与显著的竞争性外周α1拮抗作用一致。15毫克和30毫克剂量的平均剂量比分别为2.99和5.48。α1阻断的pA2为7.3。基于这些数据,乌拉地尔降压作用的主要机制可能是外周血管系统中的α1拮抗作用。