Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Brain Res. 2010 Apr 30;1328:171-80. doi: 10.1016/j.brainres.2010.02.086. Epub 2010 Mar 6.
Spontaneously epileptic rats (SER) are double mutants with both tonic convulsion and absence-like seizures from the age of 8 weeks. Hippocampal CA3 neurons in SER display a long-lasting depolarizing shift accompanied by repetitive firing (attributed to abnormalities of the Ca(2+) channels) with a single stimulation of the mossy fibers. In the present investigation, we examined if the seizure discharges of SER were correlated with the hippocampal abnormality of SER using electrophysiological and histological methods. In CA1 neurons of seizure-susceptible mature SER, higher-voltage (<8-11 V) stimulations induced a long depolarization shift (in 25% of neurons) with repetitive firing (in 12.5% of neurons). However, the tremor rat, one of the parent strains of SER, did not exhibit such abnormal firing in the CA3 region of the hippocampus. The number of CA3 neurons in SER was significantly (p<0.01) lower than that in tremor rats and Wistar rats, although no significant difference was established in the hilus. Sprouting of mossy fiber was observed in the dentate of mature SER; however, negligible staining was spotted in the dentate of both mature tremor and Wistar rats. Interestingly, expression of the brain-derived neurotrophic factor was higher in the hilus, CA3, and granular cell layer of dentate gyrus in SER than normal Wistar rats. The expression levels of TUNEL, bax, and Caspase-3 did not show significant changes between the SER and Wistar rats. SER exhibited hippocampal sclerosis-like changes which did not have enough potential for epileptogenesis. Repetitive tonic seizures and vulnerable CA3 neurons of SER could be involved in the induction of sclerosis-like changes in the hippocampus.
自发性癫痫大鼠(SER)是从 8 周龄起既有强直性惊厥又有无抽搐性发作的双重突变体。SER 的海马 CA3 神经元在单个苔藓纤维刺激下显示出持久的去极化漂移,伴随着重复放电(归因于 Ca(2+)通道的异常)。在本研究中,我们使用电生理和组织学方法检查了 SER 的癫痫发作是否与 SER 的海马异常有关。在易发性成熟 SER 的 CA1 神经元中,较高电压(<8-11V)刺激诱导长时去极化漂移(在 25%的神经元中)和重复放电(在 12.5%的神经元中)。然而,SER 的亲本品系之一震颤大鼠在海马 CA3 区没有表现出这种异常放电。SER 的 CA3 神经元数量明显(p<0.01)低于震颤大鼠和 Wistar 大鼠,尽管在齿状回的门区没有显著差异。成熟 SER 的齿状回中观察到苔藓纤维的发芽;然而,在成熟震颤和 Wistar 大鼠的齿状回中几乎没有发现染色。有趣的是,SER 中脑源性神经营养因子在门区、CA3 和颗粒细胞层的表达水平高于正常 Wistar 大鼠。TUNEL、bax 和 Caspase-3 的表达水平在 SER 和 Wistar 大鼠之间没有显著变化。SER 表现出类似于海马硬化的变化,但没有足够的致痫潜力。SER 的重复强直性发作和易损 CA3 神经元可能参与了海马硬化样变化的诱导。