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阿托品和甲硫米特对麻醉猫迷走神经诱导的胃酸分泌和胃泌素释放的影响。

Effect of atropine and methiamide on vagally induced gastric acid secretion and gastrin release in anesthetized cats.

作者信息

Uvnäs-Wallensten K, Andersson H

出版信息

Acta Physiol Scand. 1977 Apr;99(4):496-502. doi: 10.1111/j.1748-1716.1977.tb10403.x.

Abstract

Gastrin release and HCl secretion was induced by electrical vagal stimulation in anesthetized cats. Both atropine (0.1-0.3 mg/kg) and methiamide (4-20 mg/kg) inhibited the HCl secretion (by approximately 60 and approximately 80 %). On the other hand, neither atropine (0.2-2 mg/kg) nor methiamide (20 mg/kg) inhibited the vagally induced gastrin release. Possible explanations of the atropine resistance of the vagal gastrin release mechanism are discussed.

摘要

在麻醉猫中,电刺激迷走神经可诱导胃泌素释放和盐酸分泌。阿托品(0.1 - 0.3毫克/千克)和甲硫酰胺(4 - 20毫克/千克)均抑制盐酸分泌(分别约抑制60%和约80%)。另一方面,阿托品(0.2 - 2毫克/千克)和甲硫酰胺(20毫克/千克)均不抑制迷走神经诱导的胃泌素释放。文中讨论了迷走神经胃泌素释放机制对阿托品产生抗性的可能解释。

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