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某些天然肽对麻醉大鼠胃的作用。

Action of some natural peptides on the stomach of the anaesthetized rat.

作者信息

Bertaccini G, Coruzzi G

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Jun;298(2):163-6. doi: 10.1007/BF00508624.

Abstract

Different peptides of natural origin were studied for their stimulant activity on the stomach of the anaesthetized rat. The group of the tachykinins (substance P and its analogues) showed a noticeable spasmogenic activity on the whole stomach from the fundus to the pylorus. Threshold doses ranged between 0.1 and 5 microgram/kg by i.v. route and the order of potency was: eledoisin greater than phyllomedusin greater than physalaemin greater than uperolein greater than substance P. A good correlation between the dose and the duration of the spasmogenic effect was always observed and tachyphylaxis never occurred. Experiments carried out with different kinds of inhibitors suggested that tachykinins act directly on the smooth muscle of the stomach. Taking into account also results obtained in other experimental conditions it was possible to state that the N-terminal part of the molecule of these peptides has a certain importance in determining the degree of their potency in the different tests. The peptide motilin, which does not belong to the family from a chemical point of view, was scarcely active, if at all, in modifying the motility of the rat stomach.

摘要

研究了不同天然来源的肽对麻醉大鼠胃的刺激活性。速激肽组(P物质及其类似物)对从胃底到幽门的整个胃显示出明显的致痉挛活性。静脉注射途径的阈剂量在0.1至5微克/千克之间,效力顺序为:eledoisin>phyllomedusin>physalaemin>uperolein>P物质。始终观察到剂量与致痉挛效应持续时间之间有良好的相关性,且从未发生快速耐受性。用不同种类的抑制剂进行的实验表明,速激肽直接作用于胃的平滑肌。考虑到在其他实验条件下获得的结果,可以指出这些肽分子的N端部分在确定它们在不同试验中的效力程度方面具有一定重要性。从化学角度来看不属于该家族的胃动素肽,在改变大鼠胃的运动方面几乎没有活性(如果有活性的话)。

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