Captopril does not acutely modulate plasma endothelin-1 concentration in human congestive heart failure
O Grenier, F Pousset, R Isnard, H Kalotka… - … drugs and therapy, 1996 - Springer
O Grenier, F Pousset, R Isnard, H Kalotka, A Carayon, G Maistre, P Lechat, C Guerot…
Cardiovascular drugs and therapy, 1996•SpringerCongestive heart failure (CHF) is a syndrome characterized by increased levels of
angiotensin II (Ang II) and endothelin-1 (ET-1). In vitro, Ang II stimulates ET-1 release. The
purpose of this study was to assess the effect of a single dose of an angiotensin-converting
enzyme inhibitor (ACEI) captopril versus placebo on plasma endothelin concentration in
human congestive heart failure. Captopril (25 mg, given orally) was compared with placebo
in a group of 20 patients with systolic dysfunction in a double-blind randomized study …
angiotensin II (Ang II) and endothelin-1 (ET-1). In vitro, Ang II stimulates ET-1 release. The
purpose of this study was to assess the effect of a single dose of an angiotensin-converting
enzyme inhibitor (ACEI) captopril versus placebo on plasma endothelin concentration in
human congestive heart failure. Captopril (25 mg, given orally) was compared with placebo
in a group of 20 patients with systolic dysfunction in a double-blind randomized study …
Summary
Congestive heart failure (CHF) is a syndrome characterized by increased levels of angiotensin II (Ang II) and endothelin-1 (ET-1). In vitro, Ang II stimulates ET-1 release. The purpose of this study was to assess the effect of a single dose of an angiotensin-converting enzyme inhibitor (ACEI) captopril versus placebo on plasma endothelin concentration in human congestive heart failure. Captopril (25 mg, given orally) was compared with placebo in a group of 20 patients with systolic dysfunction in a double-blind randomized study. Plasma irET concentration was significantly increased in CHF patients compared with normal subjects (5.59 pg/ml±0.35 vs. 3.58 pg/ml±0.99, p<0.0002). Despite the decrease in systolic blood pressure and the increase in plasma renin activity, suggesting a significant blockade of the renin-angiotensin system, no difference in plasma irET-1 was observed between captopril and placebo. Our results suggest that captopril does not acutely influence irET-1 plasma concentration in human CHF. These data do not support the hypothesis that the acute vasodilator effect of a single dose of 25 mg of captopril given orally involves modulation of the increased plasma concentration of endothelin observed in CHF.
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