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苯海拉明在中枢神经系统中的转运。

Transport of diphenhydramine in the central nervous system.

作者信息

Goldberg M J, Spector R, Chiang C K

出版信息

J Pharmacol Exp Ther. 1987 Mar;240(3):717-22.

PMID:3559970
Abstract

The transport and metabolism of diphenhydramine was studied in vitro in the isolated rabbit choroid plexus and in vivo in New Zealand white rabbits and Sprague-Dawley rats. In vitro, [14C] diphenhydramine was accumulated by a saturable, energy-requiring system in choroid plexus. In vivo, 20 min after intraventricular injection into rabbits, [14C]diphenhydramine was cleared from cerebrospinal fluid much more rapidly than [3H]sucrose, a molecule transported in the central nervous system by simple diffusion. In vivo, employing the in situ rat brain perfusion technique, [14C]diphenhydramine was cleared from the cerebral perfusion fluid as rapidly as [14C]diazepam. However, the clearance of [14C]diphenhydramine, but not [14C]diazepam, was inhibited by the addition of 10 mM unlabeled diphenhydramine to the perfusate. These in vivo and in vitro results show that diphenhydramine, unlike diazepam, is transported between blood, brain and cerebrospinal fluid, in part, by saturable, carrier-mediated transport processes at both the blood-brain and blood-cerebrospinal fluid barriers.

摘要

在体外,利用分离的兔脉络丛进行了苯海拉明的转运和代谢研究,并在体内以新西兰白兔和斯普拉格-道利大鼠进行了相关研究。在体外,[14C]苯海拉明通过脉络丛中一种可饱和的、需要能量的系统进行积累。在体内,给兔子脑室内注射[14C]苯海拉明20分钟后,其从脑脊液中的清除速度比[3H]蔗糖快得多,[3H]蔗糖是一种通过简单扩散在中枢神经系统中转运的分子。在体内,采用大鼠原位脑灌注技术,[14C]苯海拉明从脑灌注液中的清除速度与[14C]地西泮一样快。然而,向灌注液中添加10 mM未标记的苯海拉明可抑制[14C]苯海拉明的清除,但对[14C]地西泮的清除无影响。这些体内和体外研究结果表明,与地西泮不同,苯海拉明在血脑屏障和血脑脊液屏障中,部分是通过可饱和的、载体介导的转运过程在血液、脑和脑脊液之间进行转运的。

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