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血管紧张素转换酶抑制与血管紧张素II拮抗联合应用对钠缺乏正常血压者血压及肾素释放的相加作用

Additive effects of combined angiotensin-converting enzyme inhibition and angiotensin II antagonism on blood pressure and renin release in sodium-depleted normotensives.

作者信息

Azizi M, Chatellier G, Guyene T T, Murieta-Geoffroy D, Ménard J

机构信息

Broussais Hospital Clinical Investigation Center, Assistance Publique des Hôpitaux de Paris, France.

出版信息

Circulation. 1995 Aug 15;92(4):825-34. doi: 10.1161/01.cir.92.4.825.

Abstract

BACKGROUND

Angiotensin-converting enzyme (ACE) inhibitors do not decrease plasma angiotensin (Ang) II levels 24 hours after drug intake to the same extent as at peak. This intermittent partial "escape" is explained either by a renin-mediated reactive rise in plasma Ang I or by non-ACE-dependent Ang II generation. We therefore tested the hypothesis that a combination of ACE inhibition and Ang II blockade may have additive biological and hemodynamic effects.

METHODS AND RESULTS

In a single-dose, double-blind, randomized, four-way, crossover study, an Ang II antagonist (losartan 50 mg), an ACE inhibitor (captopril 50 mg), their combination, and matched placebos were orally administered to 12 normotensive male volunteers maintained in mild sodium depletion. When captopril 50 mg and losartan 50 mg were given alone, the magnitude of their effects on blood pressure, plasma active renin, Ang I, and aldosterone was similar, whereas the kinetics of their effects were different, reflecting differences in drug pharmacokinetics. The losartan-captopril combination completely suppressed the rise in plasma Ang II induced by losartan 2 hours after drug intake (3.3 +/- 3.6 pg/mL versus 20.3 +/- 19.1 pg/mL, respectively, P < .05). Six hours after drug intake, the losartan-captopril combination induced a significantly greater decrease in mean blood pressure than that produced by either losartan or captopril alone (73 +/- 7 mm Hg versus 79 +/- 8 mm Hg versus 81 +/- 7 mm Hg, respectively, P < .05). The maximum placebo-subtracted falls in mean blood pressure for the losartan-captopril combination, captopril 50 mg, and losartan 50 mg were 14 +/- 5 mm Hg, 10 +/- 3 mm Hg, and 9 +/- 6 mm Hg, respectively (F2.22 = 3.45, P < .05). The duration of the mean blood pressure fall was not prolonged by the combination. After combined losartan-captopril administration, the area under the plasma active renin versus time curve (0 to 24 hours) was significantly increased when compared with either losartan or captopril alone (6404 +/- 2961 pg.h.mL-1 versus 3105 +/- 1461 pg.h.mL-1 versus 2092 +/- 867 pg.h.mL-1, respectively, P < .05). The combination had no additive effects on plasma aldosterone decrease when compared with either losartan or captopril alone (58 +/- 17% versus 51 +/- 20% versus 53 +/- 21%, respectively, NS).

CONCLUSIONS

The combined administration of a standard single oral dose of an ACE inhibitor and an Ang II antagonist to mildly sodium-depleted normal subjects (1) had a major additive effect on plasma renin rise, (2) induced an additional mean blood pressure reduction, and (3) had no additive effect on plasma aldosterone fall.

摘要

背景

血管紧张素转换酶(ACE)抑制剂在服药24小时后降低血浆血管紧张素(Ang)II水平的程度不如在峰值时那样显著。这种间歇性的部分“逃逸”现象,要么是由肾素介导的血浆Ang I反应性升高所致,要么是由非ACE依赖性的Ang II生成引起。因此,我们检验了以下假设:ACE抑制与Ang II阻断联合应用可能具有相加的生物学和血流动力学效应。

方法与结果

在一项单剂量、双盲、随机、四交叉研究中,对12名轻度钠缺乏的血压正常男性志愿者口服给予一种Ang II拮抗剂(氯沙坦50 mg)、一种ACE抑制剂(卡托普利50 mg)、二者的联合制剂以及匹配的安慰剂。单独给予50 mg卡托普利和50 mg氯沙坦时,它们对血压、血浆活性肾素、Ang I和醛固酮的作用强度相似,但其作用动力学不同,这反映了药物药代动力学的差异。氯沙坦 - 卡托普利联合制剂在服药2小时后完全抑制了氯沙坦诱导的血浆Ang II升高(分别为3.3±3.6 pg/mL和20.3±19.1 pg/mL,P<.05)。服药6小时后,氯沙坦 - 卡托普利联合制剂导致的平均血压下降幅度显著大于单独使用氯沙坦或卡托普利时(分别为73±7 mmHg、79±8 mmHg和81±7 mmHg,P<.05)。氯沙坦 - 卡托普利联合制剂、50 mg卡托普利和50 mg氯沙坦相对于安慰剂的最大平均血压下降值分别为14±5 mmHg、10±3 mmHg和9±6 mmHg(F2,22 = 3.45,P<.05)。联合制剂并未延长平均血压下降的持续时间。联合给予氯沙坦和卡托普利后,血浆活性肾素 - 时间曲线下面积(0至24小时)与单独使用氯沙坦或卡托普利相比显著增加(分别为6404±2961 pg·h·mL-1、3105±1461 pg·h·mL-1和2092±867 pg·h·mL-1,P<.05)。与单独使用氯沙坦或卡托普利相比,联合制剂对血浆醛固酮降低无相加作用(分别为58±17%、51±20%和53±21%,无显著性差异)。

结论

对轻度钠缺乏的正常受试者标准单剂量口服ACE抑制剂和Ang II拮抗剂联合给药,(1)对血浆肾素升高有主要的相加作用;(2)导致额外的平均血压降低;(3)对血浆醛固酮降低无相加作用。

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