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氟哌啶醇、氯丙嗪、丙咪嗪和锂对红细胞儿茶酚-O-甲基转移酶的体外作用。

In vitro effect of haloperidol, chlorpromazine, imipramine and lithium on the erythrocyte catechol-O-methyltransferase.

作者信息

Hoo J J, Noldt P, Beckermann W J, Agarwal D P, Goedde H W

出版信息

Arzneimittelforschung. 1982;32(6):681-3.

PMID:7202372
Abstract

Haloperidol, chlorpromazine, imipramine and lithium in concentrations similar to the average therapeutic plasma levels did not exert any in vitro inhibition on the erythrocyte catechol-O-methyltransferase (COMT). The inhibitory effects of haloperidol, chlorpromazine and imipramine were noted first at concentrations 1000-10 000 times their respective average therapeutic plasma levels. Unlike the former three psychotropic drugs, lithium exerted an in vitro inhibition already at a concentration 40 times the average therapeutic plasma level and that in a competitive way. The inhibitory effect of lithium could be neutralized by increasing the magnesium concentration, likewise in a competitive way.

摘要

氟哌啶醇、氯丙嗪、丙咪嗪和锂在与平均治疗血浆水平相似的浓度下,对红细胞儿茶酚-O-甲基转移酶(COMT)没有任何体外抑制作用。氟哌啶醇、氯丙嗪和丙咪嗪的抑制作用首先在其各自平均治疗血浆水平的1000 - 10000倍浓度时被观察到。与前三种精神药物不同,锂在平均治疗血浆水平的40倍浓度时就已经产生体外抑制作用,且是以竞争性方式。锂的抑制作用可以通过增加镁浓度以同样的竞争性方式来中和。

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