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大鼠口服和肌肉注射丙咪嗪、氯米帕明及其单甲基化代谢产物后的血液和脑内浓度

Blood and brain concentrations of imipramine, clomipramine and their monomethylated metabolites after oral and intramuscular administration in rats.

作者信息

Nagy A

出版信息

J Pharm Pharmacol. 1977 Feb;29(2):104-7. doi: 10.1111/j.2042-7158.1977.tb11255.x.

Abstract

Imipramine and clomipramine were administered to rats by the oral and intramuscular routes as single and multiple doses. The concentrations of both drugs and their active demethylated metabolites desipramine and desmethylclomipramine were measured in blood plasma, blood cells and brain. The concentrations of the metabolites were higher and the concentrations of the parent substances lower after oral than after parenteral administration, both in blood and in brain. In brain imipramine, despiramine and clomipramine during continuous treatment exceeded their plasma concentrations by six to ten times. The corresponding figure for desmethylclomipramine was 1-7. The extent of accumulation of the investigated substances in the brain was independent of the route of administration.

摘要

将丙咪嗪和氯米帕明以单次和多次剂量经口服和肌肉注射途径给予大鼠。测定了血浆、血细胞和脑中这两种药物及其活性去甲基代谢产物地昔帕明和去甲氯米帕明的浓度。口服给药后,血液和脑中代谢产物的浓度均高于母体物质,且在血液和脑中,口服给药后代谢产物的浓度高于非肠道给药后母体物质的浓度。在持续治疗期间,脑中的丙咪嗪、去甲丙咪嗪和氯米帕明浓度比血浆浓度高出6至10倍。去甲氯米帕明的相应倍数为1至7。所研究物质在脑中的蓄积程度与给药途径无关。

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