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组胺受体激动剂对离体灌注兔肾中肾上腺素能递质释放的影响。

Alternation by histamine receptor agonists of the release of adrenergic transmitter in the isolated perfused rabbit kidney.

作者信息

Ercan Z S, Türker R K

出版信息

Arch Int Pharmacodyn Ther. 1981 Feb;249(2):203-12.

PMID:6452863
Abstract

The effects of histamine and synthetic H1 and H2-receptor agonists on the release of neurotransmitter were studied in the isolated perfused rabbit kidney. The increase in perfusion pressure and the contraction of the venous outflow-superfused rabbit aortic strip were taken as the parameters for the evaluation of the elaboration of neuromediator from the kidney du to periarterial stimulation. Histamine and te specific histamine H1-receptor agonist, 2-(2-thiazolyl) ethylamine, caused a significant increase but the specific H2-receptor agonists, dimaprit and impromidine, produced a significant decrease in the response due to periarterial stimulation without altering that of exogenously applied noradrenaline. Prior addition of mepyramine to the medium prevented effect of 2-(2-thiazolyl) ethylamine but caused a high significant decrease in the response produced by histamine when compared with the control values. Prior addition of metiamide to the medium, however, prevented the inhibitory effect of dimaprit and impromidine but potentiated the effect of histamine. From these results it was concluded that histamine has a presynaptic H1-mediated facilitatory and H2-mediated inhibitory effects on the release of neurotransmitter from adrenergic neurons in the isolated perfused rabbit kidney.

摘要

在离体灌注兔肾中研究了组胺及合成的H1和H2受体激动剂对神经递质释放的影响。灌注压力的升高及静脉流出道超灌注兔主动脉条的收缩被用作评估肾因动脉周围刺激而释放神经介质的参数。组胺及特异性组胺H1受体激动剂2-(2-噻唑基)乙胺可引起显著增加,而特异性H2受体激动剂二甲双胍和英普咪定在不改变外源性应用去甲肾上腺素反应的情况下,可使动脉周围刺激引起的反应显著降低。预先向培养基中加入美吡拉敏可阻止2-(2-噻唑基)乙胺的作用,但与对照值相比,组胺产生的反应显著降低。然而,预先向培养基中加入甲硫咪胺可阻止二甲双胍和英普咪定的抑制作用,但增强组胺的作用。从这些结果得出结论,组胺对离体灌注兔肾中肾上腺素能神经元神经递质的释放具有突触前H1介导的促进作用和H2介导的抑制作用。

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