Zeng Ling-Hui, Rensing Nicholas R, Wong Michael
Department of Neurology and the Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 2009 May 27;29(21):6964-72. doi: 10.1523/JNEUROSCI.0066-09.2009.
Understanding molecular mechanisms mediating epileptogenesis is critical for developing more effective therapies for epilepsy. We recently found that the mammalian target of rapamycin (mTOR) signaling pathway is involved in epileptogenesis, and mTOR inhibitors prevent epilepsy in a mouse model of tuberous sclerosis complex. Here, we investigated the potential role of mTOR in a rat model of temporal lobe epilepsy initiated by status epilepticus. Acute kainate-induced seizures resulted in biphasic activation of the mTOR pathway, as evident by an increase in phospho-S6 (P-S6) expression. An initial rise in P-S6 expression started approximately 1 h after seizure onset, peaked at 3-6 h, and returned to baseline by 24 h in both hippocampus and neocortex, reflecting widespread stimulation of mTOR signaling by acute seizure activity. After resolution of status epilepticus, a second increase in P-S6 was observed in hippocampus only, which started at 3 d, peaked 5-10 d, and persisted for several weeks after kainate injection, correlating with the development of chronic epileptogenesis within hippocampus. The mTOR inhibitor rapamycin, administered before kainate, blocked both the acute and chronic phases of seizure-induced mTOR activation and decreased kainate-induced neuronal cell death, neurogenesis, mossy fiber sprouting, and the development of spontaneous epilepsy. Late rapamycin treatment, after termination of status epilepticus, blocked the chronic phase of mTOR activation and reduced mossy fiber sprouting and epilepsy but not neurogenesis or neuronal death. These findings indicate that mTOR signaling mediates mechanisms of epileptogenesis in the kainate rat model and that mTOR inhibitors have potential antiepileptogenic effects in this model.
了解介导癫痫发生的分子机制对于开发更有效的癫痫治疗方法至关重要。我们最近发现,雷帕霉素的哺乳动物靶点(mTOR)信号通路参与癫痫发生,并且mTOR抑制剂可预防结节性硬化症小鼠模型中的癫痫发作。在此,我们研究了mTOR在由癫痫持续状态引发的颞叶癫痫大鼠模型中的潜在作用。急性海藻酸诱导的癫痫发作导致mTOR通路的双相激活,磷酸化S6(P-S6)表达增加即为明证。癫痫发作开始后约1小时,P-S6表达开始初步上升,在3-6小时达到峰值,并在24小时时在海马体和新皮质中均恢复至基线水平,这反映了急性癫痫发作活动对mTOR信号的广泛刺激。癫痫持续状态缓解后,仅在海马体中观察到P-S6的第二次增加,其始于第3天,在第5-10天达到峰值,并在注射海藻酸后持续数周,这与海马体内慢性癫痫发生的发展相关。在海藻酸给药前给予mTOR抑制剂雷帕霉素,可阻断癫痫发作诱导的mTOR激活的急性和慢性阶段,并减少海藻酸诱导的神经元细胞死亡、神经发生、苔藓纤维出芽以及自发性癫痫的发展。在癫痫持续状态终止后进行雷帕霉素后期治疗,可阻断mTOR激活的慢性阶段,并减少苔藓纤维出芽和癫痫发作,但对神经发生或神经元死亡无影响。这些发现表明,mTOR信号介导了海藻酸大鼠模型中的癫痫发生机制,并且mTOR抑制剂在该模型中具有潜在的抗癫痫发生作用。