Effects of Radical Scavengers, TA248 and TA276, on Stunned Myocardium in Dogs : Involvement of K_<ATP> Channels
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概要
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TA248 (7-(β-<sc>D</sc>-glucopyranosyloxy)-4-hydroxy-3-octyloxy-2H-1-benzopyran-2-one) and TA276 (sodium 7-hydroxy-3-octyloxy-2H-1-benzopyran-2-one-4-oxide) were newly developed as radical scavengers. In vitro, TA276 scavenged both superoxide anions (· O2−) and hydroxyl radicals (· OH). TA248 also trapped · O2−, but had less activity on · OH. In vivo, left ventricular contractile functions were determined in pentobarbital-anesthetized open-chest dogs. A regional portion of the left ventricular wall was made ischemic for 20 min by ligating the left anterior descending coronary artery and then reperfused for 60 min. TA248 (3 mg/kg) and TA276 (3 mg/kg) injected i.v. 10 min before occlusion significantly improved myocardial stunning that is contractile dysfunction observed after reperfusion following brief ischemia. Glibenclamide (1 mg/kg) injected i.v. 20 min before occlusion significantly worsened the myocardial stunning. Pretreatment with glibenclamide completely abolished the beneficial effect of TA276 on myocardial stunning, whereas it only partially attenuated that of TA248, showing some improvement even in the presence of glibenclamide. Because of the incomplete scavenging activity of TA248, residual · OH may play some roles in improvement of myocardial stunning with TA248 in the presence of glibenclamide. We speculate that the · OH may eject glibenclamide from its binding site on KATP channels, leading to opening of the channels.
- 社団法人 日本薬理学会の論文
- 2002-10-01
著者
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ICHIHARA Kazuo
Department of Pharmacology, Asahikawa Medical College
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SATOH Kumi
Department of Pharmacology, Hokkaido College of Pharmacy
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Satoh Kumi
Division Of Pharmacology Hokkaido Pharmaceutical University School Of Pharmacy
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Satoh Kumi
Department Of Pharmacology Hokkaido Institute Of Pharmaceutical Sciences:department Of Pharmacology
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Aoki Y
Central Research Laboratories Dainippon Ink And Chemicals Inc.
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Satoh Kiyotaka
Division Of Pharmacology Hokkaido Pharmaceutical University School Of Pharmacy
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Ichihara K
Division Of Pharmacology Hokkaido Pharmaceutical University School Of Pharmacy
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Ichihara Kazuo
Department Of Clinical Pharmacology Asahikawa Medical College
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KANETA Shigeru
Department of Pharmacotherapeutics, Hokkaido College of Pharmacy
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Kaneta Shigeru
Division Of Pharmacology Hokkaido Pharmaceutical University School Of Pharmacy
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Kaneta Shigeru
Department Of Pharmacotherapeutics Hokkaido College Of Pharmacy
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KANO Seiichiro
Division of Pharmacology, Hokkaido Pharmaceutical University School of Pharmacy
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KOSUGI Tetsuro
Department of Pharmacology, Hokkaido College of Pharmacy
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AOKI Yasuo
Central Research Laboratories, Dainippon Ink and Chemicals, Inc.
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TAKAGAKI Hidetusge
Central Research Laboratories, Dainippon Ink and Chemicals, Inc.
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Takagaki Hidetusge
Central Research Laboratories Dainippon Ink And Chemicals Inc.
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Kosugi Tetsuro
Department Of Pharmacology Hokkaido College Of Pharmacy
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Kano Seiichiro
Division Of Pharmacology Hokkaido Pharmaceutical University School Of Pharmacy
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Kaneta Shigeru
Department of Pharmacology, Hokkaido College of Pharmacy
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