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大鼠胃分泌“体外”:组胺与通过不同机制起作用的各种抗分泌剂之间的相互作用。

Rat gastric secretion "in vitro": interaction between histamine and various antisecretagogues acting by different mechanisms.

作者信息

Coruzzi G, Adami M, Bertaccini G, Canfield S P

出版信息

Pharmacol Res Commun. 1985 Nov;17(11):1027-41. doi: 10.1016/0031-6989(85)90109-2.

Abstract

The interaction between histamine and various antisecretagogues acting by different mechanisms has been investigated in the isolated fundus from the rat stomach. Histamine evoked a concentration-dependent stimulatory effect which was competitively antagonized by the H2-receptor antagonist, ranitidine and non competitively by the H+/K+-ATPase inhibitor, omeprazole. The histamine induced secretion was highly resistant to the action of the calcium entry blocker verapamil, somatostatin and KSCN, but some inhibition was obtained with the calmodulin antagonist, trifluoperazine. Removal of calcium ions from the bathing media (both mucosal and serosal) greatly enhanced histamine-induced gastric secretion. The results suggest that the relationship between receptor stimulation and the intracellular events leading to acid secretion is far from being elucidated.

摘要

在大鼠胃离体胃底中,研究了组胺与通过不同机制起作用的各种抗分泌剂之间的相互作用。组胺引起浓度依赖性刺激作用,H2受体拮抗剂雷尼替丁对其有竞争性拮抗作用,H⁺/K⁺-ATP酶抑制剂奥美拉唑对其有非竞争性拮抗作用。组胺诱导的分泌对钙通道阻滞剂维拉帕米、生长抑素和硫氰酸钾的作用具有高度抗性,但钙调蛋白拮抗剂三氟拉嗪有一定抑制作用。从浴液介质(黏膜和浆膜)中去除钙离子可大大增强组胺诱导的胃分泌。结果表明,受体刺激与导致胃酸分泌的细胞内事件之间的关系远未阐明。

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