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丙咪嗪与血浆蛋白及脑组织的结合:与人体脑脊液中三环类药物水平的关系。

Binding of imipramine to plasma protein and to brain tissue: relationship to CSF tricyclic levels in man.

作者信息

Potter W Z, Muscettola G, Goodwin F K

出版信息

Psychopharmacology (Berl). 1979 May 25;63(2):187-92. doi: 10.1007/BF00429700.

Abstract

The possible clinical significance of the plasma protein binding of tricyclic antidepressants has been evaluated using imipramine (IMI), a typical tricyclic. Using equilibrium dialysis, the in vitro binding of IMI to plasma was compared to that of brain tissue. Cerebrospinal fluid (CSF) IMI was used as an independent measure of 'free' drug in the central nervous system. Intrinsic metabolic clearances were calculated on the basis of steady-state plasma IMI concentrations. There were three significant results: (1) variations in plasma binding are not great; (2) plasma protein binding does not limit the entry of IMI into the CSF; (3) variations in metabolism (intrinsic clearance) account for almost all variations in CSF concentrations of drug. It is concluded that measurement of free tricyclic antidepressant is not indicated in studies of clinical efficacy.

摘要

已使用典型三环类药物丙咪嗪(IMI)评估了三环类抗抑郁药血浆蛋白结合的潜在临床意义。采用平衡透析法,将IMI在体外与血浆的结合情况与脑组织的结合情况进行比较。脑脊液(CSF)中的IMI被用作中枢神经系统中“游离”药物的独立指标。基于稳态血浆IMI浓度计算内在代谢清除率。有三个重要结果:(1)血浆结合的变化不大;(2)血浆蛋白结合并不限制IMI进入脑脊液;(3)代谢(内在清除率)的变化几乎解释了脑脊液中药物浓度的所有变化。得出的结论是,在临床疗效研究中无需测定游离三环类抗抑郁药。

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