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[与神经疾病相关的线粒体苯二氮䓬受体(MBR)]

[Mitochondrial benzodiazepine receptors (MBR) in association with neurological disorders].

作者信息

Yoshii M, Nakamoto Y, Watabe S, Mugishima G, Habu H, Shiotani T, Nabeshima T

机构信息

Department of Neurophysiology, Tokyo Institute of Psychiatry, Japan.

出版信息

Nihon Shinkei Seishin Yakurigaku Zasshi. 1998 Apr;18(2):49-54.

PMID:9656233
Abstract

Ro 5-4864, a specific agonist of the peripheral-type benzodiazepine receptor (PBR), elicited convulsions 2.6 times more potently in EL mice (an animal model of epilepsy) than in DDY mice (control animal). A binding assay revealed a 50% higher density of [3H] Ro 5-4864 binding sites in the mitochondrial fraction (i.e., mitochondrial benzodiazepine receptors; MBR) of the brain tissues in EL mice as compared with DDY mice. On an elevated plus-maze, EL mice showed fear responses similar to those increased in DDY mice after PBR stimulation, suggesting a hyperfunction of MBR underlying the abnormal behaviors of EL mice. In fluorometric studies using NG108-15 cells, Ro 5-4864 depolarized mitochondrial membranes and, possibly as a consequence of this, raised intracellular Ca2+. Finally, we propose that MBR could be a major target of therapy for various neurological disorders, so drugs such as "mitochondrial membrane stabilizers" should be developed.

摘要

外周型苯二氮䓬受体(PBR)的特异性激动剂Ro 5-4864在EL小鼠(一种癫痫动物模型)中引发惊厥的效力比在DDY小鼠(对照动物)中高2.6倍。结合试验显示,与DDY小鼠相比,EL小鼠脑组织线粒体部分(即线粒体苯二氮䓬受体;MBR)中[3H]Ro 5-4864结合位点的密度高50%。在高架十字迷宫实验中,EL小鼠表现出的恐惧反应与PBR刺激后DDY小鼠增强的恐惧反应相似,这表明MBR功能亢进是EL小鼠异常行为的基础。在使用NG108-15细胞的荧光研究中,Ro 5-4864使线粒体膜去极化,可能因此导致细胞内Ca2+升高。最后,我们提出MBR可能是各种神经疾病治疗的主要靶点,因此应开发“线粒体膜稳定剂”等药物。

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