Pan Enhui, Puranam Ram S, McNamara James O
Department of Neurology, Duke University School of Medicine, Durham, NC 27710.
Department of Neurology, Duke University School of Medicine, Durham, NC 27710
eNeuro. 2022 Jan 12;9(1). doi: 10.1523/ENEURO.0375-21.2021. Print 2022 Jan-Feb.
Insight into the cellular and circuit mechanisms underlying development of temporal lobe epilepsy (TLE) will provide a foundation for improved therapies. We studied a model in which an episode of prolonged seizures is followed by recovery lasting two weeks before emergence of spontaneous recurrent seizures. We focused on the interval between the prolonged seizures and the late onset recurrent seizures. We investigated the hippocampal mossy fiber CA3 pyramidal cell microcircuit in models spanning , , and preparations. Expression of channelrhodopsin-2 in the dentate granule cells of mice enabled the selective activation of mossy fiber axons. studies revealed marked potentiation of mossy fiber evoked field potentials in hippocampal CA3 beginning within hours following seizures, a potentiation which persisted at least 7 d. Stimulation of mossy fibers in hippocampal slices using patterns of activity mimicking seizures induced LTP not only of the monosynaptic EPSC but also of the disynaptic IPSC of CA3 pyramidal cells. studies of slices isolated following seizures revealed evidence of LTP of mossy fiber evoked EPSC and disynaptic IPSC of CA3 pyramidal cells. We suggest that activation of dentate granule cells during seizures induces these plasticities and the retained balance of synaptic excitation and inhibition limits excessive activation of CA3 pyramidal cells, thereby protecting animals from spontaneous recurrent seizures at this interval following status epilepticus.
深入了解颞叶癫痫(TLE)发生发展的细胞和环路机制将为改进治疗方法奠定基础。我们研究了一种模型,在该模型中,长时间癫痫发作后会有两周的恢复时间,之后才会出现自发性反复癫痫发作。我们关注长时间癫痫发作与迟发性反复癫痫发作之间的间隔。我们在涵盖不同脑片制备的模型中研究了海马苔藓纤维CA3锥体细胞微环路。在成年小鼠的齿状颗粒细胞中表达通道视紫红质-2能够选择性激活苔藓纤维轴突。研究发现,癫痫发作后数小时内,海马CA3区苔藓纤维诱发的场电位显著增强,这种增强至少持续7天。在海马脑片中,使用模拟癫痫发作的活动模式刺激苔藓纤维,不仅诱导了CA3锥体细胞单突触兴奋性突触后电流(EPSC)的长时程增强(LTP),还诱导了双突触抑制性突触后电流(IPSC)的LTP。对癫痫发作后分离的脑片进行的研究揭示了CA3锥体细胞苔藓纤维诱发的EPSC和双突触IPSC的LTP证据。我们认为,癫痫发作期间齿状颗粒细胞的激活诱导了这些可塑性变化,并且突触兴奋和抑制的保留平衡限制了CA3锥体细胞的过度激活,从而在此癫痫持续状态后的间隔期保护动物免受自发性反复癫痫发作。