Suppr超能文献

新型咪唑啉衍生物替扎尼定对麻醉大鼠中枢刺激胃酸分泌的抑制作用

Reduction of centrally-stimulated gastric acid secretion by tizanidine, a new imidazoline derivative, in anesthetized rats.

作者信息

Maeda-Hagiwara M, Watanabe H, Kanaoka R, Watanabe K

出版信息

Arch Int Pharmacodyn Ther. 1985 Oct;277(2):321-7.

PMID:3933446
Abstract

The effect of a novel imidazoline derivative (tizanidine) on stimulated gastric acid secretion was studied in the perfused stomach of anesthetized rats. Tizanidine, which did not prevent peripherally-stimulated gastric acid secretion, inhibited 2DG- or TRH-stimulated gastric acid secretion. Yohimbine and phentolamine reduced the inhibition of TRH-stimulated acid secretion by tizanidine. Clonidine was found to have similar effects to tizanidine at a lower dose. These results indicate that tizanidine may inhibit gastric acid secretion via the central alpha-adrenergic system similar to clonidine in anesthetized rats.

摘要

在麻醉大鼠的灌流胃中研究了一种新型咪唑啉衍生物(替扎尼定)对刺激胃酸分泌的影响。替扎尼定不能阻止外周刺激引起的胃酸分泌,但能抑制2-脱氧葡萄糖(2DG)或促甲状腺激素释放激素(TRH)刺激的胃酸分泌。育亨宾和酚妥拉明可减轻替扎尼定对TRH刺激的胃酸分泌的抑制作用。发现可乐定在较低剂量时与替扎尼定有相似的作用。这些结果表明,在麻醉大鼠中,替扎尼定可能通过与可乐定类似的中枢α-肾上腺素能系统抑制胃酸分泌。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验