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内源性组胺可能参与可乐定对离体兔主动脉的肌otropic作用。 (注:这里“myotropic”可能有误,推测正确单词或许是“myotropic”,若有误请按正确内容调整翻译,整体翻译思路是先直译每个单词,再根据语境调整通顺表述)

Possible involvement of endogenous histamine in the myotropic effect of clonidine on the isolated rabbit aorta.

作者信息

Bökesoy T A, Ercan Z S, Ersoy F, Zengil H, Türker R K

出版信息

Agents Actions. 1978 Oct;8(5):478-83. doi: 10.1007/BF02111432.

Abstract

Clonidine has a contractile effect in the isolated rabbit aorta which can be blocked by alpha-adrenergic antagonist, phentolamine. Histamine H1-receptor blocker, mepyramine, partly antagonizes its myotropic effect and histamine H2-blocker, metiamide, potentiates it, implying a histaminergic component in the response. Inhibition of histamine synthesis by histidine decarboxylase inhibitor, GYKI 11.121, reduces clonidine-induced contraction in this preparation, while diamine oxidase inhibition by aminoguanidine potentiates it. This is indirect evidence of the possibility of de novo histamine synthesis by clonidine, which may take part on the contractile effect of the drug in the rabbit aorta.

摘要

可乐定对离体兔主动脉有收缩作用,该作用可被α-肾上腺素能拮抗剂酚妥拉明阻断。组胺H1受体阻滞剂美吡拉敏可部分拮抗其对平滑肌的作用,而组胺H2阻滞剂甲硫米特则增强该作用,这表明反应中存在组胺能成分。组氨酸脱羧酶抑制剂GYKI 11.121抑制组胺合成,可降低可乐定在此制剂中诱导的收缩,而氨基胍抑制二胺氧化酶则增强该收缩。这是可乐定可能重新合成组胺的间接证据,而组胺可能参与了该药物对兔主动脉的收缩作用。

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