Adrenoceptor blocking and cardiovasucular effects of the optical isomers of amosulalol (YM-09538), a combined .ALPHA.- and .BETA.-adrenoceptor blocking agent, and the corresponding desoxy derivative (YM-11133) in rats.
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概要
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The pharmacological activities of the enantiomers of amosulalol (YM-09538), a combined α- and β-adrenoceptor antagonist, and the corresponding desoxy derivative (YM-11133) were investigated in the cardiovascular system of rats. The optical isomers of amosulalol and YM-11133 antagonized the vasopressor effect of phenylephrine and the positive chronotropic effect of isoproterenol in normotensive pithed rats. Based on DR<SUB>2</SUB> values (μg/kg, i.v.) obtained from Schild plots, (+)-amosulalol and YM-11133 (DR<SUB>2</SUB>=30) were approximately 10 times more potent than (-)-amosulalol (DR<SUB>2</SUB>=324) in blocking α<SUB>1</SUB>-adrenoceptors. For β<SUB>1</SUB>-adrenoceptors, in contrast, (-)-amosulalol (DR<SUB>2</SUB>=107) was approximately 60 times more potent than (+)-amosulalol (DR<SUB>2</SUB>=6460), which was almost equipotent with YM-1 1133 (DR2=3250). The results indicate that the optical isomers of amosulalol interact differently with α- and β-adrenoceptors. The effects of these phenethylamines on blood pressure and heart rate were studied in urethaneanesthetized rats (i.v.). The rank order of hypotensive potency in anesthetized rats ((+)-=desoxy>(-)-form) was consistent with the rank order of α<SUB>1</SUB>-adrenoceptor antagonism in pithed rats. In contrast, (-)-amosulalol having a more potent β<SUB>1</SUB>-adrenoceptor antagonist activity than (+)-amosulalol and YM-11133 only produced dose-dependent bradycardia at the hypotensive doses. The results indicate that the vascular α<SUB>1</SUB>- and cardiac β<SUB>1</SUB> -adrenoceptor blocking activities of the optical isomers of amosulalol contribute to their hypotensive and bradycardia, respectively. Thus, the racemate of amosulalol appears to exert an overall activity reflecting the activities of the individual isomers.
- 公益社団法人 日本薬理学会の論文
著者
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Inagaki Osamu
Department Of Chemical Pharmacology Faculty Of Pharmaceutical Sciences The University Of Tokyo:(pres
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Takeda Masaaki
Department Of Electrical Engineering Nagoya University
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TAKENAKA Toichi
Department of Pharmacology and Biochemistry, Central Research Laboratories, Yamanouchi Pharmaceutica
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HONDA Kazuo
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo
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SHIBASAKI Masayuki
Department of Anesthesiology and Intensive Care, Kyoto Prefectural University of Medicine
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TAKENAKA Toichi
Department of Pharmacology, Central Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd.
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NAKAGAWA Chieko
Department of Pharmacology, Central Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd.
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SHIBASAKI Masayuki
Department of Pharmacology, Central Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd.
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HONDA Kazuo
Department of Pharmacology, Central Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd.
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INAGAKI Osamu
Department of Pharmacology, Central Research Laboratories, Yamanouchi Pharmaceutical Co., Ltd.
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