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[Gastrin/CCK-B receptor antagonists for a novel antiulcer agent].

作者信息

Miyata K, Nishida A, Honda K

机构信息

Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., Tsukuba, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1995 Sep;106(3):171-80. doi: 10.1254/fpj.106.171.

DOI:10.1254/fpj.106.171
PMID:8529962
Abstract

Gastrin plays an important role in gastrointestinal functions such as gastric secretion and mucosal growth. The hypergastrinemia that results from long-term treatment with proton pump inhibitors and histamine H2-receptor antagonists induces hyperplasia of enterochromaffin-like (ECL) cells and increases the secretory response to pentagastrin (acid rebound). Recently, potent and selective gastrin/CCK-B-receptor antagonists, L-365,260, PD136450 and YM022, have been developed. These compounds inhibit basal and meal-stimulated acid secretion as well as pentagastrin-stimulated acid secretion in rats and dogs. Long-term treatment with gastrin/CCK-B-receptor antagonists does not cause hyperplasia of ECL cells and acid rebound at all. Moreover, they prevent hyperplasia and acid rebound induced by proton pump inhibitors and histamine H2-receptor antagonists. Therefore, gastrin/CCK-B-receptor antagonists are suggested to be novel antiulcer and antisecretory agents without potential for acid rebound, hyperplasia and carcinoid.

摘要

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1
[Gastrin/CCK-B receptor antagonists for a novel antiulcer agent].
Nihon Yakurigaku Zasshi. 1995 Sep;106(3):171-80. doi: 10.1254/fpj.106.171.
2
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