Inhibition of agonist-induced positive inotropy by a selective Rho-associated kinase inhibitor, Y-27632

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Abstract

We examined the effect of Y-27632 ((+)-(R)-trans-4-(1-aminoethyl)-N-(4-pyridyl)cyclo-hexanecarboxamide), a selective Rho-associated kinase (ROCK) inhibitor, on agonist-induced inotropy in isolated mouse left atria. Endothelin-1, angiotensin-II, and prostaglandin F2α (PGF2α) produced positive inotropy, which was significantly attenuated by Y-27632 (100 μM). On the other hand, isoproterenol-induced positive inotropy was not attenuated by the drug. These results provide the first evidence that the Rho/ROCK pathway is involved in endothelin-1-, angiotensin-II-, and PGF2α-induced positive inotropy, but not in β-adrenoceptor-mediated positive inotropy.

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Nishimaru, K., Tanaka, Y., Tanaka, H., & Shigenobu, K. (2003). Inhibition of agonist-induced positive inotropy by a selective Rho-associated kinase inhibitor, Y-27632. Journal of Pharmacological Sciences, 92(4), 424–427. https://doi.org/10.1254/jphs.92.424

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