Morgan J M, Palmisano M, Piraino A, Hirschhorn W, Spencer S, Prasad P P, Ortiz M, Lloyd P
Department of Medicine, Allegheny University of the Health Sciences, Philadelphia, PA 19129, USA.
Clin Pharmacol Ther. 1997 Jan;61(1):35-44. doi: 10.1016/S0009-9236(97)90180-6.
Valsartan is an oral antagonist of angiotensin II that competes with angiotensin II for the AT1-receptor and is being developed as an antihypertensive agent. This study assessed the ability of 80 mg valsartan to inhibit the pressor effect of exogenous angiotensin II in healthy normotensive men, first after a single dose and then after multiple doses once daily for 7 days.
This was a single-center, double-blind, placebo-controlled, randomized crossover study. Six healthy men underwent angiotensin II challenges to determine a suitable dose required to increase their systolic blood pressure by approximately 30 mm Hg. Each subject then received an 80 mg dose of valsartan or matching placebo. The inhibition of the angiotensin II pressor effect was determined by the systolic blood pressure response to repeated angiotensin II challenges at multiple time points.
Systolic blood pressure responses to angiotensin II challenges after single and multiple doses of valsartan were significantly lower than placebo, indicating that valsartan blocked the blood pressure response to angiotensin II. The maximum blocking effect was observed within 2 to 3 hours. Mean data suggested that differences in effect between valsartan and placebo were similar after both single and multiple doses and persisted up to 24 hours after administration. The angiotensin II blocking effect was maintained up to this time, despite low plasma valsartan levels and minimal accumulation after multiple doses.
Valsartan, 80 mg, is a potent angiotensin II antagonist with a rapid onset of action and persistent angiotensin II inhibition up to 24 hours. There is no attenuation of this effect after multiple doses.
缬沙坦是一种血管紧张素II口服拮抗剂,可与血管紧张素II竞争AT1受体,目前正作为一种抗高血压药物进行研发。本研究评估了80mg缬沙坦对健康血压正常男性中外源性血管紧张素II升压作用的抑制能力,首先是单次给药后,然后是每日一次多次给药7天后。
这是一项单中心、双盲、安慰剂对照、随机交叉研究。六名健康男性接受血管紧张素II激发试验,以确定将其收缩压升高约30mmHg所需的合适剂量。然后,每位受试者接受80mg剂量的缬沙坦或匹配的安慰剂。通过在多个时间点对重复的血管紧张素II激发试验的收缩压反应来确定血管紧张素II升压作用的抑制情况。
单次和多次服用缬沙坦后,对血管紧张素II激发试验的收缩压反应显著低于安慰剂,表明缬沙坦阻断了对血管紧张素II的血压反应。在2至3小时内观察到最大阻断效果。平均数据表明,单次和多次给药后缬沙坦与安慰剂之间的效果差异相似,且在给药后24小时内持续存在。尽管血浆缬沙坦水平较低且多次给药后蓄积极少,但血管紧张素II阻断作用在此期间一直维持。
80mg缬沙坦是一种有效的血管紧张素II拮抗剂,起效迅速,对血管紧张素II的抑制作用可持续24小时。多次给药后这种作用不会减弱。