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两种H(+)-K(+)-ATP酶抑制剂、一种M1选择性抗毒蕈碱药和一种H2受体拮抗剂对大鼠溃疡愈合作用的直接比较。

Direct comparison between the ulcer-healing effects of two H(+)-K(+)-ATPase inhibitors, one M1-selective antimuscarinic and one H2 receptor antagonist in the rat.

作者信息

Kromer W, Gönne S, Riedel R, Postius S

机构信息

Department of Pharmacology, Byk Gulden Pharmaceuticals, Konstanz, FRG.

出版信息

Pharmacology. 1990;41(6):333-7. doi: 10.1159/000138750.

Abstract

A direct comparison of the ulcer-healing effects of two H(+)-K(+)-ATPase inhibitors (pantoprazole and omeprazole), one M1 antimuscarinic (telenzepine) and one H2 receptor antagonist (cimetidine) was performed in the rat. Gastric and duodenal ulcers were induced by local application of acetic acid and thereafter treated over 10 days by the test drugs. Overall and on a molar basis, ulcer healing was comparably accelerated by pantoprazole, omeprazole and telenzepine and less so by cimetidine. The same rank order was found with respect to the inhibition of gastric acid secretion in the modified Shay rat.

摘要

在大鼠中对两种H(+)-K(+)-ATP酶抑制剂(泮托拉唑和奥美拉唑)、一种M1抗毒蕈碱药(替仑西平)和一种H2受体拮抗剂(西咪替丁)的溃疡愈合效果进行了直接比较。通过局部应用乙酸诱导大鼠胃溃疡和十二指肠溃疡,然后用受试药物治疗10天。总体而言,按摩尔计算,泮托拉唑、奥美拉唑和替仑西平可同等程度地加速溃疡愈合,而西咪替丁的作用则较弱。在改良的Shay大鼠中,关于胃酸分泌抑制作用也发现了相同的排序。

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