Inhibition of myocardial endothelin pathway improves long-term survival in heart failure

Nature. 1996 Nov 28;384(6607):353-5. doi: 10.1038/384353a0.


Occlusion of the diseased coronary artery in humans causes acute myocardial infarction, survivors of which have a high risk for the development of chronic heart failure. Cardiac myocytes and vascular endothelial cells produce endothelin-1 (refs 2-4), which increases the contractility of cardiac muscle and of vascular smooth muscle cells. Endothelin-1 also exerts long-term effects such as myocardial hypertrophy, and causes cellular injury in cardiac myocytes. Production of endothelin-1 is markedly increased in the myocardium of rats with heart failure, and acute application of an endothelin-receptor antagonist decreases myocardial contractility in such rats, indicating that myocardial endothelin-1 may help to support contractility of the failing heart. But we report here that the upregulated myocardial endothelin system may contribute to the progression of chronic heart failure, because long-term treatment with an endothelin-receptor antagonist greatly improved the survival of rats with chronic heart failure. This beneficial effect was accompanied by significant amelioration of left ventricular dysfunction and prevention of ventricular remodelling, in which there is usually an increase in the ventricular mass and cavity enlargement of the ventricle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiac Output, Low / drug therapy*
  • Cardiac Output, Low / metabolism
  • Cardiac Output, Low / physiopathology
  • Cardiomegaly / prevention & control
  • Endothelin Receptor Antagonists*
  • Endothelin-1 / antagonists & inhibitors*
  • Endothelin-1 / genetics
  • Heart Ventricles / drug effects
  • Heart Ventricles / pathology
  • Hemodynamics / drug effects
  • Male
  • Myocardial Infarction / physiopathology
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Peptides, Cyclic / therapeutic use*
  • RNA, Messenger / metabolism
  • Rats
  • Receptor, Endothelin A
  • Survival Analysis
  • Time Factors


  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Peptides, Cyclic
  • RNA, Messenger
  • Receptor, Endothelin A
  • cyclo(Trp-Asp-Pro-Val-Leu)