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内皮素A受体拮抗作用与血管紧张素转换酶抑制作用通过内皮素B受体介导和一氧化氮依赖机制产生协同作用。

Endothelin A receptor antagonism and angiotensin-converting enzyme inhibition are synergistic via an endothelin B receptor-mediated and nitric oxide-dependent mechanism.

作者信息

Goddard Jane, Eckhart Corine, Johnston Neil R, Cumming Allan D, Rankin Andrew J, Webb David J

机构信息

Centre for Cardiovascular Science, University of Edinburgh, UK.

出版信息

J Am Soc Nephrol. 2004 Oct;15(10):2601-10. doi: 10.1097/01.ASN.0000141313.84470.4B.

Abstract

Animal studies suggest that endothelin A (ETA) receptor antagonism and angiotensin-converting enzyme (ACE) inhibition may be synergistic. This interaction and the role of ETB receptors and endothelial mediators were investigated in terms of systemic and renal effects in humans in two studies. In one study, six subjects received placebo, the ETA receptor antagonist BQ-123 alone, and BQ-123 in combination with the ETB receptor antagonist BQ-788 after pretreatment with the ACE inhibitor enalapril (E) or placebo. In the other, six subjects who were pretreated with E received placebo, BQ-123, and BQ-123 with concomitant inhibition of nitric oxide (NO) synthase or cyclo-oxygenase (COX). Both were randomized, double-blind, crossover studies. Mean arterial pressure was reduced by BQ-123, an effect that was doubled during ACE inhibition (mean area under curve +/- SEM; BQ-123, -2.3 +/- 1.8%; BQ-123+E, -5.1 +/- 1.1%; P < 0.05 versus placebo). BQ-123 increased effective renal blood flow (BQ-123, -0.1 +/- 2.4%; BQ-123+E, 10.9 +/- 4.2%; P < 0.01 versus BQ-123), reduced effective renal vascular resistance (BQ-123, -1.2 +/- 3.1%; BQ-123+E, -12.8 +/- 3.0%; P < 0.01 versus placebo and versus BQ-123), and increased urinary sodium excretion markedly (BQ-123, 2.6 +/- 12.8%; BQ-123+E, 25.2 +/- 12.6%; P < 0.05 versus BQ-123, P < 0.01 versus placebo and versus E) only during ACE inhibition. These effects were abolished by both ETB receptor blockade and NO synthase inhibition, whereas COX inhibition had no effect. In conclusion, the combination of ETA receptor antagonism and ACE inhibition is synergistic via an ETB receptor-mediated, NO-dependent, COX-independent mechanism. The reduction of BP and renal vascular resistance and associated substantial natriuresis make this a potentially attractive therapeutic combination in renal disease.

摘要

动物研究表明,内皮素A(ETA)受体拮抗作用与血管紧张素转换酶(ACE)抑制作用可能具有协同性。在两项针对人体全身和肾脏效应的研究中,对这种相互作用以及ETB受体和内皮介质的作用进行了调查。在一项研究中,6名受试者在接受血管紧张素转换酶抑制剂依那普利(E)或安慰剂预处理后,分别接受安慰剂、单独的ETA受体拮抗剂BQ - 123以及与ETB受体拮抗剂BQ - 788联合使用的BQ - 123。在另一项研究中,6名接受E预处理的受试者分别接受安慰剂、BQ - 123以及同时抑制一氧化氮(NO)合酶或环氧化酶(COX)的BQ - 123。两项研究均为随机、双盲、交叉研究。BQ - 123可降低平均动脉压,在ACE抑制期间这种作用增强一倍(平均曲线下面积±标准误;BQ - 123,-2.3±1.8%;BQ - 123 + E,-5.1±1.1%;与安慰剂相比,P < 0.05)。BQ - 123可增加有效肾血流量(BQ - 123,-0.1±2.4%;BQ - 123 + E,10.9±4.2%;与BQ - 123相比,P < 0.01),降低有效肾血管阻力(BQ - 123,-1.2±3.1%;BQ - 123 + E,-12.8±3.0%;与安慰剂和BQ - 123相比,P < 0.01),并且仅在ACE抑制期间显著增加尿钠排泄(BQ - 123,2.6±12.8%;BQ - 123 + E,25.2±12.6%;与BQ - 123相比,P < 0.05,与安慰剂和E相比,P < 0.01)。ETB受体阻断和NO合酶抑制均消除了这些作用,而COX抑制则无作用。总之,ETA受体拮抗作用与ACE抑制作用的联合通过ETB受体介导、NO依赖、COX非依赖的机制具有协同性。血压和肾血管阻力的降低以及相关的显著利钠作用使其在肾脏疾病中成为一种潜在有吸引力的治疗组合。

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