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口服氯米帕明后大鼠脑和血清中氯米帕明及其主要代谢产物去甲氯米帕明的稳态浓度。

Steady state concentrations of clomipramine and its major metabolite desmethylclomipramine in rat brain and serum after oral administration of clomipramine.

作者信息

Weigmann H, Härtter S, Bagli M, Hiemke C

机构信息

Department of Psychiatry, University of Mainz, Untere Zahlbacher Strasse 8, D-55131 Mainz, Germany.

出版信息

Eur Neuropsychopharmacol. 2000 Sep;10(5):401-5. doi: 10.1016/s0924-977x(00)00098-5.

Abstract

Twenty male Sprague-Dawley rats received five oral doses of clomipramine 20 mg/kg at 4-h intervals. The animals were decapitated 1, 2, 3, 5 and 12 h after the last dose for determination of clomipramine and desmethylclomipramine in serum and frontal cerebral cortex. Time dependent concentrations of clomipramine and desmethylclomipramine paralleled in serum and brain. Half-lives were similar in serum and brain with 7.8 versus 6.2 h and 5.5 versus 5.0 h for clomipramine and desmethylclomipramine, respectively. Absolute concentrations, however, were markedly higher in brain than in serum - 12.5 fold for clomipramine and 7.4 fold for desmethylclomipramine. The data indicate that serum and brain concentrations of clomipramine and its demethylated metabolite are rapidly exchanged between blood and brain. Assuming that blood and brain kinetics in man and rat are comparable, it is concluded that monitoring blood concentrations of clomipramine and desmethylclomipramine is a useful way to evaluate brain concentrations.

摘要

二十只雄性斯普拉格-道利大鼠每隔4小时口服5次氯米帕明,剂量为20毫克/千克。在最后一剂后的1、2、3、5和12小时将动物断头,以测定血清和额叶皮质中的氯米帕明和去甲氯米帕明。氯米帕明和去甲氯米帕明在血清和脑中的浓度随时间变化呈平行关系。氯米帕明和去甲氯米帕明在血清和脑中的半衰期相似,分别为7.8小时对6.2小时和5.5小时对5.0小时。然而,绝对浓度在脑中明显高于血清——氯米帕明高12.5倍,去甲氯米帕明高7.4倍。数据表明,氯米帕明及其去甲基代谢物在血清和脑中的浓度在血液和脑之间迅速交换。假设人和大鼠的血液和脑动力学具有可比性,得出结论:监测氯米帕明和去甲氯米帕明的血药浓度是评估脑内浓度的一种有用方法。

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