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溴化诺林、西咪替丁和奥芬溴铵对大鼠某些促分泌剂诱导的胃酸分泌过多的影响。

Effect of nolinium bromide, cimetidine, and oxyphencyclimine on gastric hypersecretion induced by some secretagogues in the rat.

作者信息

Goldenberg M M, Moore R B

出版信息

Arch Int Pharmacodyn Ther. 1980 Sep;247(1):163-76.

PMID:7004367
Abstract

Gastric hypersecretion was induced in the pylorus-ligated rat by histamine, pentagastrin, carbachol, or insulin following the peroral administration of either nolinium bromide, a new non-anticholinergic antisecretory drug, cimetidine, an H2-histamine receptor antagonists, or oxyphencyclimine hydrochloride, a specific anticholinergic drug. Nolinium bromide cimetidine or oxyphencycline. Nolinium bromide and cimetidine weakly antagonized hypersecretions in response to carbachol and to insulin while oxyphencyclimine caused profound antagonism. It was concluded that there was incomplete parallelism in inhibitory efficacy among the three antagonist drugs suggesting that their modes of action in blocking gastric hypersection differed. The findings with nolinium bromide were consistent with its lack of specific anticholinergic action and in keeping with its gastric acid antisecretory activity.

摘要

在幽门结扎的大鼠中,通过组胺、五肽胃泌素、卡巴胆碱或胰岛素诱导胃酸分泌过多,此前分别经口给予一种新型非抗胆碱能抗分泌药物溴诺林、H2组胺受体拮抗剂西咪替丁或特异性抗胆碱能药物盐酸羟苯环胺。溴诺林、西咪替丁或羟苯环素。溴诺林和西咪替丁对卡巴胆碱和胰岛素引起的胃酸分泌过多有微弱的拮抗作用,而盐酸羟苯环胺则产生显著的拮抗作用。得出的结论是,三种拮抗剂药物的抑制效果不完全平行,这表明它们阻断胃酸分泌过多的作用方式不同。溴诺林的研究结果与其缺乏特异性抗胆碱能作用一致,也与其胃酸抗分泌活性相符。

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