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胆囊收缩素和胃泌素抑制组胺刺激的离体兔胃腺对氨基比林的摄取。

Cholecystokinin and gastrin inhibit histamine stimulated aminopyrine uptake in isolated rabbit gastric glands.

作者信息

Bengtsson P, Nilsson G

机构信息

Department of Physiology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, Uppsala.

出版信息

Ups J Med Sci. 1989;94(2):111-22. doi: 10.3109/03009738909178556.

Abstract

In the present study we have analyzed if cholecystokinin (CCK) or gastrin (G) can inhibit acid production in isolated rabbit gastric glands as revealed by the aminopyrine technique. The results show that G 17 I, CCK 8 NS, CCK 8 S, ceruletide and CCK 39 significantly inhibit histamine induced aminopyrine accumulation. No significant inhibition was noted for G 4, G 34 and NT G 1-13. As a group the CCK peptides were more effective than the gastrin peptides in inhibiting the aminopyrine uptake. CCK 8 S and ceruletide, the most potent inhibitors, reduced histamine induced aminopyrine accumulation with an ED50 of 10(-9) and 10(-10) M respectively. These potencies are similar to those by which CCK peptides stimulate isolated pancreatic acini to secrete amylase. Inhibition evoked by CCK 8 S was most effective following 20-40 min of incubation time, possibly indicating that the effect is mediated by the release of an intermediate substance. The results may therefore indicate a role for cholecystokinin as a physiological inhibitor of acid secretion in the rabbit. The results may also contribute to explain why the potent gastric secretagogue gastrin per se fails to stimulate acid formation in gastric glands isolated from the rabbit.

摘要

在本研究中,我们通过氨基比林技术分析了胆囊收缩素(CCK)或胃泌素(G)是否能抑制离体兔胃腺的胃酸分泌。结果显示,G 17 I、CCK 8 NS、CCK 8 S、蛙皮素和CCK 39能显著抑制组胺诱导的氨基比林蓄积。而G 4、G 34和NT G 1 - 13未观察到明显抑制作用。作为一个整体,CCK肽在抑制氨基比林摄取方面比胃泌素肽更有效。CCK 8 S和蛙皮素是最有效的抑制剂,它们使组胺诱导的氨基比林蓄积减少,其半数有效浓度(ED50)分别为10^(-9) M和10^(-10) M。这些效力与CCK肽刺激离体胰腺腺泡分泌淀粉酶的效力相似。CCK 8 S引起的抑制作用在孵育20 - 40分钟后最为有效,这可能表明该作用是由一种中间物质的释放介导的。因此,这些结果可能表明胆囊收缩素在兔胃酸分泌中作为一种生理性抑制剂发挥作用。这些结果也可能有助于解释为什么强效胃泌素本身不能刺激从兔分离出的胃腺中的胃酸形成。

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