Folbergrová Jaroslava, Druga Rastislav, Otáhal Jakub, Haugvicová Renata, Mares Pavel, Kubová Hana
Institute of Physiology, Academy of Sciences of the Czech Republic, Vídenská 1083, 14220 Prague 4, Czech Republic.
Exp Neurol. 2006 Sep;201(1):105-19. doi: 10.1016/j.expneurol.2006.03.031. Epub 2006 Jun 6.
The present study has examined the effect of free radical spin trap N-tert-butyl-alpha-phenylnitrone (PBN) in the model of seizures induced in immature 12-day-old rats by bilateral intracerebroventricular infusion of dl-homocysteic acid (dl-HCA, 600 nmol/side). PBN was given i.p. in two doses (100 mg/kg each), 30 min prior and 30 min after dl-HCA infusion. PBN did not significantly influence the severity of seizures, evident both from the behavioral symptoms and EEG recordings. PBN normalized decreased ATP levels in the hippocampus, occurring during the acute phase of seizures ( approximately 45-50 min after infusion) and persisting until the end of the 24-h recovery period. PBN also led to normalization of decreased glucose levels and to a significant reduction of lactate accumulation in the cerebral cortex and hippocampus. The neuroprotective effect of PBN was evaluated after 24 h and 6 days of survival following dl-HCA-induced seizures (Nissl and Fluoro-Jade B staining). The administration of PBN resulted in a partial amelioration of severe damage observed in many brain regions following infusion of dl-HCA alone. The data suggest that increased free radical production is apparently occurring during seizures induced in immature rats by homocysteic acid. Free radical scavenger PBN had a clear-cut protective effect, evident as the improved recovery of brain energy status and as a partial, but significant, attenuation of neuronal degeneration associated with this model of seizures.
本研究检测了自由基自旋捕捉剂N-叔丁基-α-苯基硝酮(PBN)在12日龄未成熟大鼠双侧脑室内注入dl-高胱氨酸(dl-HCA,600 nmol/侧)诱导的癫痫模型中的作用。PBN以两种剂量(各100 mg/kg)腹腔注射,分别在注入dl-HCA前30分钟和注入后30分钟给药。从行为症状和脑电图记录来看,PBN对癫痫严重程度没有显著影响。PBN使癫痫急性期(注入后约45 - 50分钟)海马中降低的ATP水平恢复正常,并持续至24小时恢复期结束。PBN还使大脑皮层和海马中降低的葡萄糖水平恢复正常,并显著减少乳酸积累。在dl-HCA诱导癫痫发作后24小时和6天存活期后,通过尼氏染色和氟玉髓B染色评估PBN的神经保护作用。单独注入dl-HCA后,许多脑区出现严重损伤,而PBN给药导致这种损伤部分改善。数据表明,在同型半胱氨酸诱导未成熟大鼠癫痫发作期间,自由基生成明显增加。自由基清除剂PBN具有明确的保护作用,表现为脑能量状态恢复改善以及与该癫痫模型相关的神经元变性部分但显著减轻。