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多巴胺对犬心血管作用的一种可能模式。

A possible mode of cardiovascular actions of dopamine in dogs.

作者信息

Furukawa T, Ono N, Maeda Y, Nakahara T, Yoshihara K

出版信息

Jpn J Pharmacol. 1976 Aug;26(4):481-92. doi: 10.1254/jjp.26.481.

Abstract

A possible mode of cardiovascular actions of dopamine was studied using ephedrine. In the dog pretreated with repeated administrations of ephedrine (total dose, 40 or 80 mg/kg, i.v.) or with combined administrations of ephedrine (total dose, 90 mg/kg, s.c. and i.v.) and reserpine (2 mg/kg, s.c., 24 hr previously), pressor responses to dopamine were eliminated and reversed to depressor responses whereas depressor responses to dopamine were potentiated. Positive chronotropic effects of dopamine were almost eliminated. Pressor and positive chronotropic effects of tyramine were almost abolished. Sympathomimetic effect of noradrenaline and adrenaline were potentiated while those of isoprenaline were inhibited. In the heart-lung preparation of ephedrine-treated dogs (total dose, 40 mg/kg, i.v.), cardiac stimulating effects of dopamine and tyramine were strongly depressed, and those of noradrenaline, adrenaline and isoprenaline were reduced to some extent. In the open-chest dogs, after pretreatment of cocaine (4 mg/kg, i.v.), pressor, positive inotropic and chronotropic effects of noradrenaline were potentiated, whilst those of tyramine were inhibited. Those of dopamine were not visibly altered, but depressor, negative chronotropic and inotropic effects of dopamine appeared at small doses. In the ephedrine-pretreated dogs, these sympathomimetic effects of dopamine and tyramine after cocaine were strongly depressed and those of noradrenaline were inhibited to a certain degree. The results obtained with ephedrine suggest that dopamine differs from other catecholamines and tyramine in the mode of cardiovascular actions.

摘要

使用麻黄碱研究了多巴胺心血管作用的一种可能模式。在反复静脉注射麻黄碱(总剂量40或80mg/kg)或皮下及静脉联合注射麻黄碱(总剂量90mg/kg)与利血平(2mg/kg,皮下注射,提前24小时)预处理的犬中,对多巴胺的升压反应消失并逆转成降压反应,而对多巴胺的降压反应则增强。多巴胺的正性变时作用几乎消失。酪胺的升压和正性变时作用几乎被消除。去甲肾上腺素和肾上腺素的拟交感神经作用增强,而异丙肾上腺素的作用受到抑制。在经麻黄碱处理的犬(总剂量40mg/kg,静脉注射)的心肺制备中,多巴胺和酪胺的心脏刺激作用强烈受抑,而去甲肾上腺素、肾上腺素和异丙肾上腺素的作用在一定程度上降低。在开胸犬中,静脉注射可卡因(4mg/kg)预处理后,去甲肾上腺素的升压、正性变力和变时作用增强,而酪胺的作用受到抑制。多巴胺的作用无明显改变,但小剂量时出现多巴胺的降压、负性变时和变力作用。在经麻黄碱预处理的犬中,可卡因后多巴胺和酪胺的这些拟交感神经作用强烈受抑,而去甲肾上腺素的作用在一定程度上受到抑制。用麻黄碱获得的结果表明,多巴胺在心血管作用模式上与其他儿茶酚胺和酪胺不同。

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