Subtypes of .ALPHA.1-Adrenoceptors Involved in Noradrenaline-Induced Contractions of Rat Thoracic Aorta and Dog Carotid Artery.
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概要
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We tried to determine α<SUB>1</SUB>-adrenoceptor subtypes involved in noradrenaline-induced contractions of rat thoracic aorta and dog carotid artery. Prazosin competitively antagonized the contractions induced by noradrenaline in both the arteries with a high pK<SUB>B</SUB> value (approximately 9.7). WB4101, benoxathian, phentolamine, HV723 and 5-methylurapidil also competitively antagonized the responses to noradrenaline in both the arteries: however, the affinities for the antagonists were significantly higher in the rat thoracic aorta than in the dog carotid artery. The affinities for the competitive antagonists were not changed by treatment with nifedipine. In the rat thoracic aorta, chlorethylclonidine (CEC) elicited either a persistent contraction with rhythmic activities before treatment with nifedipine or partial inactivation of α<SUB>1</SUB>-adrenoceptors in the presence of nifedipine. On the other hand, CEC produced only inactivation of α<SUB>1</SUB>-adrenoceptors in the dog carotid artery. These results suggest that noradrenaline-induced contractions of the rat thoracic aorta and dog carotid artery are respectively mediated through distinct α<SUB>1</SUB>-adrenoceptor subtypes. According to the α<SUB>1A</SUB>, α<SUB>1B</SUB> subclassification, the α<SUB>1</SUB>-adrenoceptor of dog carotid artery is like the α<SUB>1B</SUB> subtype, while that of rat thoracic aorta is atypical. Both subtypes are also identified as a high affinity site for prazosin (α<SUB>1H</SUB> subtype) in the α<SUB>1H</SUB>, α<SUB>1L</SUB> and α<SUB>1N</SUB> subclassification.
- 公益社団法人 日本薬理学会の論文
著者
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Muramatsu Ikunobu
Department Of Pharmacology Faculty Of Medicine Kyoto University And Department Of Zoology And Its Ca
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Kigoshi Shigeru
Department Of Pharmacology Fukui Medical School
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Ohmura Tsuyoshi
Department Of Pharmacology Fukui Medical School
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