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雷尼替丁对十二指肠溃疡患者胃酸抑制的动力学

Dynamics of gastric acid inhibition by ranitidine in duodenal ulcer patients.

作者信息

Konturek S J, Obtułowicz W, Kwiecień N, Kopp B, Oleksy J

出版信息

Digestion. 1981;22(3):119-25. doi: 10.1159/000198617.

Abstract

The dynamics of the inhibitory effect of ranitidine, a new H2-receptor antagonist, on histamine and pentagastrin-induced gastric secretion have been examined in duodenal ulcer patients. The inhibition by ranitidine of histamine-induced secretion was found to be competitive, whereas that of pentagastrin-induced secretion not competitive. Ranitidine was an effective inhibitor of pentagastrin-induced secretion for 8-12 h after administration. The availability of ranitidine, a powerful and long-acting inhibitor of gastric secretion, provides an opportunity of an alternative treatment from cimetidine for peptic ulcer and related diseases.

摘要

在十二指肠溃疡患者中研究了新型H2受体拮抗剂雷尼替丁对组胺和五肽胃泌素诱导的胃酸分泌的抑制作用动力学。发现雷尼替丁对组胺诱导的分泌的抑制作用具有竞争性,而对五肽胃泌素诱导的分泌的抑制作用则无竞争性。雷尼替丁给药后8 - 12小时是五肽胃泌素诱导分泌的有效抑制剂。雷尼替丁作为一种强效长效的胃酸分泌抑制剂,为消化性溃疡及相关疾病提供了一种替代西咪替丁的治疗机会。

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