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美喹他嗪(LM - 209)的药理学研究。(V)。LM - 209的主要代谢产物美喹他嗪亚砜(LM - 209 SO)的药理作用(作者译)

[Pharmacological study of Mequitazine (LM-209). (V). Pharmacological actions of a main metabolite of LM-209, mequitazine sulfoxide (LM-209 SO) (author's transl)].

作者信息

Hojo M, Nagasaka Y, Katayama O, Serizawa I

出版信息

Nihon Yakurigaku Zasshi. 1981 Nov;78(5):431-8.

PMID:6120129
Abstract

The pharmacological action of a main metabolite of Mequitazine (LM-209), Mequitazine sulfoxide (LM-209 SO), was compared with data on LM-209 to investigate whether LM-209 is metabolized in vivo to the active form and if it has pharmacological actions. In the excised ileum of guinea-pigs, the anti-histaminic and anti-cholinergic activities of LM-209 SO were about 1/8 and 1/20, respectively, of LM-209. The protective activity of LM-209 SO on sudden death induced by histamine in mice was about 1/2.5 of LM-209. Acute toxicity of LM-209 SO given orally to mice was 1/3 of LM-209. In the EEG of rabbits, LM-209 SO did not affect the spontaneous pattern or the arousal and recruiting responses. The mydriatic and local anesthetic activities of LM-209 SO were significantly less than those of LM-209. Thus, the pharmacological activities and toxicity of LM-209 SO were significantly less potent than those of LM-209.

摘要

对美喹他嗪(LM - 209)的主要代谢产物亚砜美喹他嗪(LM - 209 SO)的药理作用与LM - 209的数据进行了比较,以研究LM - 209在体内是否代谢为活性形式以及它是否具有药理作用。在豚鼠离体回肠中,LM - 209 SO的抗组胺和抗胆碱活性分别约为LM - 209的1/8和1/20。LM - 209 SO对小鼠组胺诱导的猝死的保护活性约为LM - 209的1/2.5。口服给予小鼠的LM - 209 SO的急性毒性为LM - 209的1/3。在兔脑电图中,LM - 209 SO不影响自发模式或觉醒和募集反应。LM - 209 SO的散瞳和局部麻醉活性明显低于LM - 209。因此,LM - 209 SO的药理活性和毒性明显低于LM - 209。

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