Premium
Effects of the endothelin receptor antagonist bosentan on cardiac performance during porcine endotoxin shock
Author(s) -
Wanecek M.,
Weitzberg E.,
Alving K.,
Rudehill A.,
Oldner A.
Publication year - 2001
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1034/j.1399-6576.2001.451015.x
Subject(s) - bosentan , medicine , endothelin receptor , endothelin receptor antagonist , afterload , cardiology , shock (circulatory) , cardiac output , receptor antagonist , cardiac function curve , hemodynamics , endocrinology , antagonist , receptor , heart failure
Background: Cardiac dysfunction during septic shock is well described but the underlying mechanisms still remain to be resolved. This study was conducted to elucidate the involvement of endothelin in cardiac function during endotoxin shock by the use of endothelin receptor antagonism. Methods: Anaesthetised and haemodynamically stable landrace pigs received the nonpeptide mixed endothelin receptor antagonist bosentan, two hours after onset of endotoxaemia (n=7). Cardiopulmonary vascular changes, including cardiac index, stroke work index, coronary artery blood flow, rate of change of left ventricular pressure (dp/dt), and arterial and coronary sinus plasma levels of endothelin‐1‐like immunoreactivity were compared to a control group only receiving endotoxin (n=7). Results: Plasma endothelin‐1‐like immunoreactivity increased threefold in the control group. Bosentan effectively counteracted the endotoxin induced decrease in cardiac index. This was accompanied by a significant reduction of both right and left ventricular afterload. In addition, coronary artery blood flow increased and coronary vascular resistance decreased compared to controls. Dp/dt remained unaffected by endothelin receptor antagonism. A further increase in plasma endothelin‐1‐like immunoreactivity was seen in response to bosentan. Conclusion: These results indicate that the increased endothelin production during endotoxaemia contributes to a depressed cardiac performance and that endothelin receptor antagonism may counteract this development. Possible mechanisms for the improved cardiac performance include both a reduction of afterload and enhanced coronary blood flow.