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组胺H2受体拮抗剂与胃酸分泌——进展报告

Histamine H2-receptor antagonists and gastric acid secretion -- a progress report.

作者信息

Black J W

出版信息

Klin Wochenschr. 1976 Oct 1;54(19):911-4. doi: 10.1007/BF01469004.

Abstract

Histamine H2-receptor antagonists, including burimamide, metiamide and cimetidine, are effective antagonists of histamine-stimulated acid secretion from mammalian, avian or reptilian gastric mucosa. Acid secretion stimulated by gastrin or pentagastrin is also inhibited by these drugs, but there is disagreement about the effects of these drugs on acid secretion resulting from activation of acetylcholine receptors. Based on the pharmacological evidence possibilities of treatment by these drugs were discussed in cases with excessive stimulation of acid secretion due to high blood levels of histamine or gastrin. The positive results in several trials on Zollinger-Ellison syndrome and peptic ulcer were very impressive. Some practical problems have still to be solved, for example the appropriate phase for applying the drugs. The demonstrated clinical effectiveness, however, against peptic ulceration offers a clear alternative to surgery for many patients.

摘要

组胺H2受体拮抗剂,包括布立马胺、甲硫咪特和西咪替丁,是组胺刺激哺乳动物、鸟类或爬行动物胃黏膜分泌胃酸的有效拮抗剂。胃泌素或五肽胃泌素刺激的胃酸分泌也会被这些药物抑制,但关于这些药物对乙酰胆碱受体激活引起的胃酸分泌的影响存在分歧。基于药理学证据,讨论了在因组胺或胃泌素血药浓度高导致胃酸分泌过度刺激的情况下使用这些药物进行治疗的可能性。在佐林格-埃利森综合征和消化性溃疡的多项试验中取得的阳性结果非常令人印象深刻。一些实际问题仍有待解决,例如用药的合适阶段。然而,已证实的对消化性溃疡的临床疗效为许多患者提供了一种明显优于手术的替代方案。

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