Suppr超能文献

组胺H2受体拮抗剂

Histamine H2-receptor antagonists.

作者信息

Keithley J K

机构信息

Rush University, College of Nursing, Chicago, Illinois.

出版信息

Nurs Clin North Am. 1991 Jun;26(2):361-73.

PMID:1675461
Abstract

In summary, histamine initiates acid secretion by stimulating the H2 subtype histamine receptor on parietal cells. Cimetidine, rantidine, famotidine, and nizantidine are histamine H2-receptor antagonists that block this action of histamine, reducing gastric acid output and concentration under both basal and stimulated conditions. These agents are used for treatment and prevention of peptic and stress ulcers as well as for hypersecretory states. Because of their effectiveness and low incidence of side effects, H2-antagonists have largely replaced more traditional antiulcer regimens.

摘要

总之,组胺通过刺激壁细胞上的H2亚型组胺受体来启动胃酸分泌。西咪替丁、雷尼替丁、法莫替丁和尼扎替丁是组胺H2受体拮抗剂,它们阻断组胺的这一作用,在基础和刺激条件下均降低胃酸分泌量和浓度。这些药物用于治疗和预防消化性溃疡及应激性溃疡,以及用于胃酸分泌过多状态。由于其有效性和低副作用发生率,H2拮抗剂已在很大程度上取代了更传统的抗溃疡治疗方案。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验