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[肉碱对离体和去神经大鼠胃制剂的拟胆碱作用]

[Cholinomimetics effects of carnitine on isolated and denervated rat stomach preparations].

作者信息

Bettini V, Martino R, Norani M, Ton P, Legrenzi E

出版信息

Farmaco Sci. 1986 Jul;41(7):530-8.

PMID:3743746
Abstract

According to various suggestions in the literature of cholinomimetic effects of carnitine on nervous structures, and experimental results of previous work on vascular smooth muscle, we studied the influence of this substance on the rat isolated and denervated stomach responses to acetylcholine (Ach). We found that Ach invariably induces contraction of the preparation, this effect being abolished by means of atropine or prifinium bromide or reduced by means of fendiline or flunarizine. We found also that carnitine invariably enhances the contractile responses of the preparation to Ach, and this effect is not modified by indomethacin or lysine acetylsalicylate, but usually abolished by fendiline and flunarizine. Our opinion is that the potentiation of stomach contractile responses to Ach by carnitine, is not due to prostaglandin mediation but it is due to sensitisation of the muscarinic receptors, which are stimulating contraction (here and in vascular smooth muscle) by means of: facilitation of calcium transit across the cellular membrane; intracellular deposit site release activation.

摘要

根据文献中关于肉碱对神经结构拟胆碱作用的各种建议,以及先前对血管平滑肌研究的实验结果,我们研究了该物质对大鼠离体和去神经支配胃对乙酰胆碱(Ach)反应的影响。我们发现,Ach总是能引起标本收缩,这种作用可被阿托品或溴丙胺太林消除,或被芬地林或氟桂利嗪减弱。我们还发现,肉碱总是能增强标本对Ach的收缩反应,且这种作用不受吲哚美辛或赖氨酸乙酰水杨酸酯的影响,但通常会被芬地林和氟桂利嗪消除。我们认为,肉碱增强胃对Ach的收缩反应,并非由前列腺素介导,而是由于毒蕈碱受体的敏化,毒蕈碱受体通过以下方式刺激收缩(在胃和血管平滑肌中均如此):促进钙通过细胞膜转运;激活细胞内储存部位释放。

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