Abstract
We performed experiments to elucidate the cellular mechanism for the biphasic inotropic response to endothelin-1 of single rabbit ventricular myocytes loaded with a fluorescent dye, acetoxymethylester of indo-1. Endothelin-1 at 10 nM elicited a biphasic inotropic effect: a transient decrease in cell shortening and Ca 2+ transients followed by an increase in cell shortening without significant elevation of peak Ca 2+ transients. The selective endothelin ET A receptor antagonist FR139317 (2( R)-[2( R)-[2( S)-[(1-hexahydro-1 H-azepinyl)]carbonyl]amino-4-methylpentanoyl]amino-3-[3-(1-methyl-1 H-indolyl)propionyl]amino-3-(2-pyridyl)propionic acid) at 1 μM abolished the biphasic effect of endothelin-1 on cell shortening and Ca 2+ transients. The selective protein kinase C inhibitor chelerythrine at 1 μM and the tyrosine kinase inhibitor genistein at 5 μM inhibited the endothelin-1-induced increase in cell shortening without significantly affecting Ca 2+ transients and the transient decrease in cell shortening and Ca 2+ transients. The present results indicate that both protein kinase C and tyrosine kinase may contribute to the increase in myofilament Ca 2+ sensitivity induced by endothelin-1, whereas the decrease in Ca 2+ transients induced by endothelin-1 may be mediated by a signalling pathway different from that involved in the increase in cardiac contractility in rabbit ventricular myocytes.
Published Version
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