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哌仑西平对胃十二指肠溃疡患者胃黏膜碳酸酐酶的抑制作用。

Inhibition of gastric mucosa carbonic anhydrase by pirenzepine in patients with gastroduodenal ulcers.

作者信息

Puşcaş I, Búzás G, Surányi P, Domuta M

出版信息

Arzneimittelforschung. 1981;31(3):508-9.

PMID:6894381
Abstract

Pirenzepine (Gastrozepin) is a drug recently introduced in the therapy of gastroduodenal ulcer (GDU). Although its effect of decreasing acid secretion is clinically known, its mechanism of action remains uncertain. The authors present investigations proving by in vitro experiments carried out on pure carbonic anhydrase (CA) and on CA from human gastric mucosa that GZ is a strong inhibitor of CA. In this acceptation, GZ may be considered both an enzymatic inhibitor and an antagonist of histamine H2 receptors.

摘要

哌仑西平(胃疡平)是最近用于治疗胃十二指肠溃疡(GDU)的一种药物。尽管其减少胃酸分泌的作用在临床上已为人所知,但其作用机制仍不明确。作者通过对纯碳酸酐酶(CA)和人胃黏膜CA进行的体外实验证明,哌仑西平是CA的强效抑制剂。基于此,哌仑西平可被视为一种酶抑制剂和组胺H2受体拮抗剂。

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