Comparison of selective ETA and ETB receptor antagonists in patients with chronic heart failure

被引:28
作者
Cowburn, PJ
Cleland, JGF
McDonagh, TA
McArthur, JD
Dargie, HJ
Morton, JJ
机构
[1] Southampton Gen Hosp, Wessex Cardiothorac Ctr, Southampton SO16 6YD, Hants, England
[2] Univ Hull, Castle Hill Hosp, Dept Cardiol, Kingston Upon Hull HU5 7RX, Yorks, England
[3] Western Infirm & Associated Hosp, Dept Cardiol, London SW3 6NP, England
[4] Univ Glasgow, Med Res Council Clin Res Intiat Heart Failure, Glasgow G12 8QQ, Lanark, Scotland
关键词
endothelins; heart failure; pulmonary circulation;
D O I
10.1016/j.ejheart.2004.08.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The vasoconstrictor action of endothelin-1 (ET-1) is mediated through ETA and ETB receptor Subtypes on vascular smooth muscle. ETB receptors are also present on the vascular endothelium where they mediate vasodilation. Animal studies suggest that the ETB receptor also acts as a clearance receptor for endothelin. Aims: To investigate the effects of a selective ETA and a selective ETB receptor antagonist alone and in combination on haemodynamics and circulating concentrations of ET-1 in patients with chronic heart failure. Results: Infusion of BQ-123 (n=10), a selective ETA receptor antagonist, led to systemic vasodilation and did not change plasma ET-1 concentrations (1.38+/-0.82 to 1.38+/-0.91 fmol/ml, ns). Infusion of BQ-788 (n=8) led to systemic vasoconstriction with a rise in plasma ET-I (1.84+/-1.06 to 2.73+/-0.99 fmol/ml,p<0.01). The addition of BQ-123 to BQ-788 led to systemic and pulmonary vasodilation with no further increase in plasma ET-1 concentrations (2.80+/-1.14 to 2.90+/-1.20 fmol/ml, ns). Conclusion: The rise in plasma ET-1 concentrations in response to selective blockade of ETB receptors and the associated adverse haemodynamic effects suggest that ETB receptors have a role in the clearance of ET-1 in man and that their blockade may not be advantageous for patients with heart failure. (C) 2004 European Society of Cardiology. Published by Elsevier B.V All rights reserved.
引用
收藏
页码:37 / 42
页数:6
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