Role of endothelin in cardiovascular disease

被引:123
作者
Agapitov, AV [1 ]
Haynes, WG [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
关键词
endothelium; endothelin; antagonists; hypertension; chronic heart failure;
D O I
10.3317/jraas.2002.001
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Endothelins are a family of peptides, which comprises endothelin-1 (ET-1), endothelin-2 (ET-2) and endothelin-3 (ET 3), each containing 21 amino-acids. ET-1 is a peptide secreted mostly by vascular endothelial cells, the predominant isoform expressed in vasculature and the most potent vasoconstrictor currently known. ET-1 also has inotropic, chemotactic and mitogenic properties. In addition, it influences salt and water homeostasis through its effects on the renin-angiotensin-aldosterone system (RAAS), vasopressin and atrial natriuretic peptide and stimulates the sympathetic nervous system. The overall action of endothelia is to increase blood pressure and vascular tone. Therefore, endothelia antagonists may play an important role in the treatment of cardiac, vascular and renal diseases associated with regional or systemic vasoconstriction and cell proliferation, such as essential hypertension, pulmonary hypertension, chronic heart failure and chronic renal failure. Long-term anti-endothelia therapy may improve symptoms and favourably alter the progression of heart failure. Endothelin appears to participate in induction and progression of sclerotic renal changes, leading to progression to end-stage renal disease. Anti-endothelia therapy might offer additional benefits in the prevention of progression of chronic renal failure in addition to the known benefits of RAAS inhibition. Clinical trials have demonstrated potentially important benefits of endothelin antagonists for patients with essential hypertension, pulmonary hypertension and heart failure. Further studies are necessary to determine the role of anti-endothelia therapy in the treatment of cardiovascular diseases and determine the different roles of selective receptor antagonism vs. mixed ETA/B-receptor antagonism in human diseases.
引用
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页码:1 / 15
页数:15
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