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新型H2受体拮抗剂雷尼替丁的药理学与临床疗效

Pharmacology and clinical efficacy of ranitidine, a new H2-receptor antagonist.

作者信息

Helman C A, Tim L O

出版信息

Pharmacotherapy. 1983 Jul-Aug;3(4):185-92. doi: 10.1002/j.1875-9114.1983.tb03248.x.

Abstract

Ranitidine is a new histamine H2-receptor antagonist that includes a furan ring structure, whereas other H2-receptor antagonists include an imidazole ring. It is more potent than cimetidine in inhibiting gastric acid secretion and lacks cimetidine's anti-androgenic and hepatic microsomal enzyme inhibiting effects. In the recommended dosage of 150 mg twice daily, ranitidine is as effective as cimetidine in healing duodenal and gastric ulcers and has the advantages of less frequent dosing and fewer side effects. Ranitidine appears to be the drug of choice in the treatment of the Zollinger-Ellison syndrome because of its increased potency and lesser effect on endocrine function compared to cimetidine.

摘要

雷尼替丁是一种新型组胺H2受体拮抗剂,其含有呋喃环结构,而其他H2受体拮抗剂含有咪唑环。在抑制胃酸分泌方面,它比西咪替丁更有效,且没有西咪替丁的抗雄激素和肝微粒体酶抑制作用。在推荐剂量为每日两次,每次150毫克时,雷尼替丁在治愈十二指肠溃疡和胃溃疡方面与西咪替丁效果相同,并且具有给药频率较低和副作用较少的优点。由于与西咪替丁相比,雷尼替丁效力增强且对内分泌功能影响较小,它似乎是治疗卓艾综合征的首选药物。

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