Why the study?
Does EMD94246 improve left ventricular function and remodeling in rats with experimental myocardial infarction?
Does EMD94246 improve left ventricular function and remodeling in rats with experimental myocardial infarction?
Long-term blockade of the ETA receptor with EMD94246 worsened left ventricular dilatation in a rat model of myocardial infarction.
Raises caution for ETA blockade in post-MI remodeling; hypothesis-generating in this rat model and requires confirmation before clinical consideration.
An endothelin (ET(A)) antagonist reduced mortality and an ET(A) + ET(B) antagonist prevented left ventricular dilatation in rats with large myocardial infarction. This study tested the hypothesis that long-term blockade of the ET(A) receptor would have beneficial effects on left ventricular function and remodeling. Three hours after coronary artery ligation or sham operation in rats, EMD94246 (100 mg/kg/day, n=62) or placebo (n=62) was given by gavage. Eight weeks later, left ventricular hemodynamic measurements were performed and left ventricular volume determined with a double-lumen catheter after KCl-induced cardiac arrest. EMD94246 treatment had no effects on mortality or hemodynamic parameters. In rats with large infarcts, EMD94246 significantly increased left ventricular volume (2.5+/-0.1 vs. 2.2+/-0.1 ml/kg; p < 0.05). The nonpeptide ET(A)-selective antagonist EMD94246 promoted chronic left ventricular dilatation in rats with large myocardial infarction.
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Hu et al. (1998) studied this question.
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