Munafo A, Christen Y, Nussberger J, Shum L Y, Borland R M, Lee R J, Waeber B, Biollaz J, Brunner H R
Department of Medicine, University Hospital, CHUV, Lausanne, Switzerland.
Clin Pharmacol Ther. 1992 May;51(5):513-21. doi: 10.1038/clpt.1992.56.
The aim of this study was to investigate the relationships between plasma concentrations of losartan, an orally active angiotensin II inhibitor, its active metabolite EXP3174, and angiotensin II blockade. Six healthy subjects received single oral doses of 40, 80, or 120 mg losartan and placebo at 1-week intervals in a crossover study. Angiotensin II blockade was assessed by the blood pressure response to exogenous angiotensin II before and after losartan administration. EXP3174 reached higher plasma concentrations and was eliminated more slowly than its parent compound; its levels paralleled the profile of angiotensin II blockade closer than losartan. Inhibition of the pressure response was dose dependent. The Hill-shaped relationship between response and EXP3174 concentration (or time-integrated variables) approached a plateau with 80 mg. The dose-dependent increase in plasma renin and angiotensin II exhibited a considerable individual scatter. We conclude that losartan produces a dose-dependent, effective angiotensin II blockade that is largely determined by the active metabolite EXP3174.
本研究的目的是调查口服活性血管紧张素II抑制剂氯沙坦的血浆浓度、其活性代谢物EXP3174与血管紧张素II阻断之间的关系。在一项交叉研究中,6名健康受试者每隔1周接受40、80或120mg氯沙坦的单次口服剂量及安慰剂。通过氯沙坦给药前后对外源性血管紧张素II的血压反应来评估血管紧张素II阻断情况。EXP3174达到的血浆浓度高于其母体化合物,且消除更慢;其水平比氯沙坦更接近血管紧张素II阻断情况。压力反应的抑制呈剂量依赖性。反应与EXP3174浓度(或时间积分变量)之间的钟形关系在80mg时接近平台期。血浆肾素和血管紧张素II的剂量依赖性增加表现出相当大的个体差异。我们得出结论,氯沙坦产生剂量依赖性、有效的血管紧张素II阻断作用,这在很大程度上由活性代谢物EXP3174决定。