In Vivo Characterization of the Mitochondrial Selective KATP Opener (3R)-trans-4-((4-Chlorophenyl)-N-(1H-imidazol-2-ylmethyl)dimethyl-2H-1-benzopyran-6-carbonitril Monohydrochloride (BMS-191095): Cardioprotective, Hemodynamic, and Electrophysiological Effects
Recent studies have shown the importance of mitochondrial ATP-sensitive potassium channels (K ATP ) in cardioprotection, and studies in vitro have shown that the benzopyran analog (3 R )- trans - 4-((4-chlorophenyl)- N -(1 H -imidazol-2-ylmethyl)dimethyl-2 H -1-benzopyran-6-carbonitril monohydrochlo...
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Published in | The Journal of pharmacology and experimental therapeutics Vol. 303; no. 1; p. 132 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
American Society for Pharmacology and Experimental Therapeutics
01.10.2002
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Online Access | Get full text |
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Summary: | Recent studies have shown the importance of mitochondrial ATP-sensitive potassium channels (K ATP ) in cardioprotection, and studies in vitro have shown that the benzopyran analog (3 R )- trans - 4-((4-chlorophenyl)- N -(1 H -imidazol-2-ylmethyl)dimethyl-2 H -1-benzopyran-6-carbonitril monohydrochloride (BMS-191095) is a selective mitochondrial K ATP opener with cardioprotective activity. The goal of this study was to show selective cardioprotection for BMS-191095 in vivo
without hemodynamic or cardiac electrophysiological effects expected for nonselective K ATP openers. BMS-191095 reduced infarct size in anesthetized dogs (90-min ischemia + 5-h reperfusion) in a dose-dependent manner
(ED 25 = 0.4 mg/kg i.v.) with efficacious plasma concentrations of 0.3 to 1.0 μM, which were consistent with potency in vitro. None
of the doses of BMS-191095 tested caused any effect on peripheral or coronary hemodynamic status. Further studies in dogs
showed no effects of BMS-191095 on cardiac conduction or action potential configuration within the cardioprotective dose range.
In a programmed electrical stimulation model, BMS-191095 showed no proarrhythmic effects, which is consistent with its lack
of effects on cardiac electrophysiological status. BMS-191095 is a potent and efficacious cardioprotectant that is devoid
of hemodynamic and cardiac electrophysiological side effects of first generation K ATP openers, which open both sarcolemmal and mitochondrial K ATP . Selective opening or activation of mitochondrial K ATP seems to be a potentially effective strategy for developing well tolerated and efficacious K ATP openers. |
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ISSN: | 0022-3565 1521-0103 |
DOI: | 10.1124/jpet.102.036988 |