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[组胺H2受体拮抗剂。生理与临床方面]

[Histamine-H2-receptor antagonists. Physiological and clinical aspects].

作者信息

Domschke W, Domschke S

出版信息

Fortschr Med. 1976 Jun 17;94(18):1082-4.

PMID:964868
Abstract

Histamine-H2-receptor antagonists (Burimamide, Metiamide, Cimetidine) may inhibit histamine-stimulated gastric secretion in various species including man; in constrast, conventional antihistaminics (H1-antagonists) do not do so. Gastric secretion as stimulated by pentagastrin, insulin, 2-deoxy-glucose or an intragastrically instilled meal is also decreased by H2-antagonists, and a final common mediator role for histamine in the gastric secretory is discussed. H2-antagonists do also inhibit pancreatic enzyme secretion, but do not affect at all bicarbonate secretion. Recent clinical trials have shown Metiamide to be superior to placebo in therapy of duodenal ulcer.

摘要

组胺H2受体拮抗剂(布立马胺、甲硫米特、西咪替丁)可抑制包括人类在内的多种物种中组胺刺激的胃酸分泌;相比之下,传统抗组胺药(H1拮抗剂)则无此作用。五肽胃泌素、胰岛素、2-脱氧葡萄糖或胃内灌注食物刺激引起的胃酸分泌也会被H2拮抗剂减少,并且讨论了组胺在胃酸分泌中最终的共同介质作用。H2拮抗剂也会抑制胰腺酶分泌,但对碳酸氢盐分泌完全没有影响。最近的临床试验表明,甲硫米特在十二指肠溃疡治疗中优于安慰剂。

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