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阿扑吗啡对豚鼠心肌的正性肌力作用由多巴胺DA1受体介导。

Positive inotropic effect of apomorphine on guinea pig myocardium is mediated by dopamine DA1 receptors.

作者信息

Wang N, Zhao D H, Sheng B H

机构信息

Department of Geriatrics, Dong Fang Hospital, Fuzhou, China.

出版信息

Zhongguo Yao Li Xue Bao. 1991 May;12(3):207-11.

PMID:1781280
Abstract

Dopaminergic agonist apomorphine (Apo, 1-100 mumol.L-1) had a concentration-dependent positive inotropic effect on guinea pig left atria. This effect was not changed obviously when the influences of sympathetic and parasympathetic nerves were eliminated by reserpine and atropine, respectively. Apo had little inotropic action on guinea pig papillary muscles. The time course of positive inotropic effect of Apo was different from that of isoprenaline and phenylephrine. Apo influenced the isometric contraction curves in a different way from isoprenaline. Dopaminergic antagonist haloperidol antagonized the positive inotropic effect of Apo. This effect was also competitively antagonized by dopamine DA1 antagonist SCH 23390. While dopamine DA2 antagonist domperidone, beta-adrenergic antagonist propranolol and alpha-adrenergic antagonist phentolamine did not obviously influence the effect of Apo. We concluded that the positive inotropic effect of Apo was mediated by postsynaptic dopamine DA1 receptors in guinea pig left atria.

摘要

多巴胺能激动剂阿扑吗啡(Apo,1 - 100 μmol·L⁻¹)对豚鼠左心房具有浓度依赖性的正性肌力作用。当分别用利血平和阿托品消除交感神经和副交感神经的影响时,这种作用没有明显改变。Apo对豚鼠乳头肌几乎没有肌力作用。Apo正性肌力作用的时间进程与异丙肾上腺素和去氧肾上腺素不同。Apo影响等长收缩曲线的方式与异丙肾上腺素不同。多巴胺能拮抗剂氟哌啶醇拮抗Apo的正性肌力作用。多巴胺DA1拮抗剂SCH 23390也能竞争性拮抗这种作用。而多巴胺DA2拮抗剂多潘立酮、β-肾上腺素能拮抗剂普萘洛尔和α-肾上腺素能拮抗剂酚妥拉明对Apo的作用没有明显影响。我们得出结论,Apo的正性肌力作用是由豚鼠左心房突触后多巴胺DA1受体介导的。

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