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组胺受体激动剂和抑制剂对豚鼠胃底泌酸的影响。

The effects of stimulants and inhibitors of histamine receptors on acid secretion from guinea pig gastric fundus.

作者信息

Impicciatore M, Morini G, Bertaccini G

出版信息

Eur J Pharmacol. 1978 Apr 1;48(3):249-54. doi: 10.1016/0014-2999(78)90083-3.

Abstract

Two selective H2 receptor stimulants (5-methyl-N-methylhistamine and dimaprit) so far never tested in isolated gastric preparations, were found to be strong stimulants of acid secretion from the guinea pig isolated gastric fundus. Although some differences were observed in the cumulative dose--response curves for these two agonists, the peak responses obtained were not significantly different from the maximum response to histamine. Cimetidine produced parallel displacement of the dose--response curves to the right with the maximum response unchanged, suggesting competitive antagonism of H2 receptors. The dose--response curve for histamine was not affected by the simultaneous administration of an H1 receptor agonist, 2(2-aminoethyl)thiazole, or of an H1 receptor antagonist, pyrilamine. This indicates that the action of histamine on the isolated guinea pig gastric fundus is associated exclusively with H2 receptor stimulation.

摘要

两种选择性H2受体激动剂(5-甲基-N-甲基组胺和二甲双胍)迄今从未在离体胃制剂中进行过测试,结果发现它们是豚鼠离体胃底酸分泌的强效刺激剂。尽管在这两种激动剂的累积剂量-反应曲线上观察到了一些差异,但获得的峰值反应与组胺的最大反应并无显著差异。西咪替丁使剂量-反应曲线平行右移,最大反应不变,提示对H2受体有竞争性拮抗作用。组胺的剂量-反应曲线不受同时给予H1受体激动剂2-(2-氨基乙基)噻唑或H1受体拮抗剂吡拉明的影响。这表明组胺对离体豚鼠胃底的作用仅与H2受体刺激有关。

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