美托洛尔在大鼠脑和脑脊液中的分布。

T Nakazono, T Murakami, S Sakai, Y Higashi, N Yata
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引用次数: 2

摘要

测定了酒石酸美托洛尔(MPL)在2种不同稳态血浆浓度(2和20 nmol/ml)和静脉给药(100 nmol/kg)下大鼠脑和脑脊液(CSF)中的分布。稳态条件下,两种不同浓度血浆MPL在脑和脑脊液的分布无差异,脑或CSF-血浆分配系数分别为5.7和1.5。静脉给药后,MPL迅速分布到脑脊液中,未检测到其初始摄取期。另一方面,MPL在脑内的分布在摄取期相对缓慢。因此,使用改进的2室模型和反褶积方法分析了脑从血浆中摄取MPL的药代动力学,而由于缺乏摄取期,MPL的脑脊液分布不足以进行动力学分析。用室室模型和反褶积分析MPL的脑摄取得到了相同的结果,计算的MPL脑Kp值与稳态血浆浓度下观察到的Kp值几乎相当。体外研究认为MPL在脑脊液中的分布主要取决于血浆与脑脊液的pH差,而脑脊液与脑组织之间MPL的相互转移可以忽略不计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain and cerebrospinal fluid distributions of metoprolol in rats.

The distribution of metoprolol tartrate (MPL) into the brain and cerebrospinal fluid (CSF) from plasma was determined at 2 different steady-state plasma concentrations (2 and 20 nmol/ml) and following intravenous bolus administration (100 nmol/kg) in rats. Under steady-state condition, no difference in the brain and CSF distributions of MPL was observed between 2 different plasma MPL concentrations, and the value of brain- or CSF-to-plasma partition coefficients were 5.7 and 1.5, respectively. Following intravenous administration, MPL distributed into CSF very rapidly and its initial uptake phase was not detected. On the other hand, MPL distribution into the brain was relatively slow with the uptake phase. Thus, the brain uptake of MPL from the plasma was pharmacokinetically analyzed using a modified 2-compartment model and deconvolution method, whereas the CSF distribution of MPL was not adequate for kinetic analysis because of the lack of uptake phase. The analysis of brain uptake of MPL by both compartment model and deconvolution gave the same results and the calculated brain Kp value of MPL was almost comparable with that of observed Kp value under steady-state plasma concentration. The distribution of MPL into CSF was considered mainly depending on the pH difference between the plasma and CSF, and the mutual transfer of MPL between CSF and the brain tissue was considered to be negligible from an in vitro study.

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