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犬胃壁细胞在最大酸分泌期及使用胃分泌抑制剂 UK - 9040 后的形态学和药理学研究

Morphological and pharmacological studies of the parietal cells of the stomach in the dog during periods of maximal acid output and after the gastric secretory inhibitor UK-9040.

作者信息

Hamer D B, Price A B, Baron J H

出版信息

Gut. 1977 Feb;18(2):91-8. doi: 10.1136/gut.18.2.91.

Abstract

UK-9040, a derivative of the antihistamine triprolidine, is a potent gastric secretory inhibitor. Given orally to dogs it reduced gastric acid, pepsin and volume output in response to food, insulin, histamine, N-methyl histamine, and pentagastrin. Doses of 6-36 mg/kg administered orally four to five hours before the secretagogues produced a dose-dependant and up to 100% inhibition in the outputs of innervated gastric fistula and denervated Heidenhain pouch. Inhibition was still present 24 hours after administration of UK-9040 but was absent at 48 hours. Blood pressure and pulse rate were not affected. Studies with the electron microscope revealed that the normal ultrastructural responses to gastric secretory stimulation were arrested. UK-9040 showed no cumulative effect, tolerance did not occur, and after withdrawal of the drug the physiological and morphological gastric responses of the parietal cells rapidly returned to normal.

摘要

UK - 9040是抗组胺药曲普利啶的衍生物,是一种强效的胃分泌抑制剂。给犬口服后,它能减少因食物、胰岛素、组胺、N - 甲基组胺和五肽胃泌素引起的胃酸、胃蛋白酶分泌及胃液量。在给予促分泌剂前4至5小时口服6 - 36毫克/千克的剂量,对支配的胃瘘和去神经的海登海因小胃的分泌产生剂量依赖性且高达100%的抑制作用。在给予UK - 9040 24小时后仍有抑制作用,但48小时后则无。血压和脉搏率未受影响。电子显微镜研究显示,对胃分泌刺激的正常超微结构反应被阻断。UK - 9040没有累积效应,不会产生耐受性,停药后壁细胞的生理和形态学胃反应迅速恢复正常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80bc/1411295/52e992dd2090/gut00471-0024-a.jpg

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