Nakamoto Y, Watabe S, Shiotani T, Yoshii M
Department of Neurophysiology, Tokyo Institute of Psychiatry, Japan.
Brain Res. 1996 Apr 22;717(1-2):91-8. doi: 10.1016/0006-8993(96)00033-9.
Peripheral-type benzodiazepine receptors (PBR) in the brain were studied in association with epileptic seizures using EL mice, an animal model of epilepsy, and DDY mice as controls. Ro 5-4864 (i.p.), a specific agonist for PBR, elicited tonic-clonic convulsions in EL mice 2.6-times more potently than in DDY mice with CD50s of 11.9 and 31.2 mg/kg for EL and DDY mice, respectively. In contrast, pentylenetetrazole (i.p.) exerted convulsant actions on EL and DDY mice in a less differential way with CD50s of 29.2 and 48.1 mg/kg for EL and DDY mice, respectively. PK 11195 (i.v.), a specific antagonist for PBR, raised seizure thresholds of EL mice at a dose of 2 mg/kg. Binding assay revealed a 50% higher density of [3H]Ro 5-4864 binding sites in the mitochondrial fraction isolated from the cerebrum of EL mice in comparison with DDY mice. Similarly, a 40% higher density of [3H]flunitrazepam binding was observed in the mitochondrial fraction of EL mice. The results support the hypothesis that PBR, particularly those associated with mitochondria, are involved in the pathogenesis of epileptic seizures in EL mice.
利用癫痫动物模型EL小鼠和作为对照的DDY小鼠,研究了大脑中的外周型苯二氮䓬受体(PBR)与癫痫发作的关系。PBR的特异性激动剂Ro 5-4864(腹腔注射)诱发EL小鼠强直性阵挛性惊厥的效力比DDY小鼠高2.6倍,EL小鼠和DDY小鼠的半数惊厥剂量(CD50)分别为11.9和31.2mg/kg。相比之下,戊四氮(腹腔注射)对EL小鼠和DDY小鼠的惊厥作用差异较小,EL小鼠和DDY小鼠的CD50分别为29.2和48.1mg/kg。PBR的特异性拮抗剂PK 11195(静脉注射)在剂量为2mg/kg时提高了EL小鼠的癫痫发作阈值。结合试验显示,与DDY小鼠相比,从EL小鼠大脑分离的线粒体部分中[3H]Ro 5-4864结合位点的密度高50%。同样,在EL小鼠的线粒体部分中观察到[3H]氟硝西泮结合密度高40%。结果支持以下假设:PBR,特别是与线粒体相关的PBR,参与了EL小鼠癫痫发作的发病机制。