Inhibition of angiotensin-converting enzyme and phosphodiesterase type 5 improves endothelial function in heart failure

被引:32
作者
Hryniewicz, K
Dimayuga, C
Hudaihed, A
Androne, AS
Zheng, HY
Jankowski, K
Katz, SD [1 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Sect Cardiovasc Med, New Haven, CT 06510 USA
[2] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[3] Warsaw Univ, Dept Internal Med & Cardiol, Warsaw, Poland
关键词
angiotensin-converting enzyme (ACE); heart failure; endothelium; nitric oxide; neurohormone; phosphodiesterase (PDF);
D O I
10.1042/CS20040266
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
ACE (angiotensin-converting enzyme) inhibitors and PDE5 (phosphodiesterase type 5) inhibitors have each been reported to improve endothelial function in cardiovascular disease patients, but the comparative and combined effects of these two classes have not been studied previously. We sought to characterize the acute effects of ramipril alone, sildenafil alone, or their combination on endothelial function in patients with CHIF (chronic heart failure). CHF subjects (n = 64) were randomized to receive placebo, 10 mg of ramipril alone, 50 mg of sildenafil alone or a combination of ramipril and sildenafil in a double-blind manner. FMD (flow-mediated dilation) of the brachial artery was determined by high-resolution ultrasound imaging before and at 1, 2 and 4 h after administration of the study drug. Ramipril alone increased FMD at 4 h compared with placebo (+ 2.3 +/- 1.3%, P = 0.02). Sildenafil alone increased FMD at 1, 2 and 4 h compared with placebo (+ 3.9 +/- 1.4, + 4.6 +/- 1.8 and + 3.7 +/- 1.3% respectively, all P < 0.02). Sildenafil in combination with ramipril increased FMD at 1, 2 and 4 h when compared with placebo (+ 3.5 +/- 1.5, + 4.5 +/- 1.8 and + 4.8 +/- 1.3 % respectively, all P < 0.03). Ramipril and sildenafil both acutely improved FMD in patients with CHF, with additive effects evident at 4 h during combination therapy. Therefore further work to characterize chronic effects of combined ACE and PDE5 inhibition on endothelial function are warranted.
引用
收藏
页码:331 / 338
页数:8
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