Liu Haiyu, Tufa Uilki, Zahra Anya, Chow Jonathan, Sivanenthiran Nila, Cheng Chloe, Liu Yapg, Cheung Phinehas, Lim Stellar, Jin Yaozhong, Mao Min, Sun Yuqing, Wu Chiping, Wennberg Richard, Bardakjian Berj, Carlen Peter L, Eubanks James H, Song Hongmei, Zhang Liang
Departments of Neurosurgery, The First Hospital of Jilin University, Changchun, Jilin 130021 China.
Krembil Research Institute, University Health Network, Toronto, Ontario, Canada M5T 2S8.
Cereb Cortex Commun. 2021 Jan 22;2(1):tgab004. doi: 10.1093/texcom/tgab004. eCollection 2021.
Epilepsy is a chronic neurological disorder characterized by spontaneous recurrent seizures (SRS) and comorbidities. Kindling through repetitive brief stimulation of a limbic structure is a commonly used model of temporal lobe epilepsy. Particularly, extended kindling over a period up to a few months can induce SRS, which may simulate slowly evolving epileptogenesis of temporal lobe epilepsy. Currently, electroencephalographic (EEG) features of SRS in rodent models of extended kindling remain to be detailed. We explored this using a mouse model of extended hippocampal kindling. Intracranial EEG recordings were made from the kindled hippocampus and unstimulated hippocampal, neocortical, piriform, entorhinal, or thalamic area in individual mice. Spontaneous EEG discharges with concurrent low-voltage fast onsets were observed from the two corresponding areas in nearly all SRS detected, irrespective of associated motor seizures. Examined in brain slices, epileptiform discharges were induced by alkaline artificial cerebrospinal fluid in the hippocampal CA3, piriform and entorhinal cortical areas of extended kindled mice but not control mice. Together, these in vivo and in vitro observations suggest that the epileptic activity involving a macroscopic network may generate concurrent discharges in forebrain areas and initiate SRS in hippocampally kindled mice.
癫痫是一种慢性神经疾病,其特征为自发性反复癫痫发作(SRS)及合并症。通过对边缘结构进行重复性短暂刺激来引发点燃效应,是常用的颞叶癫痫模型。特别是,长达数月的延长点燃效应可诱发SRS,这可能模拟颞叶癫痫缓慢发展的癫痫发生过程。目前,延长点燃效应的啮齿动物模型中SRS的脑电图(EEG)特征仍有待详细研究。我们使用延长海马体点燃效应的小鼠模型对此进行了探索。对个体小鼠的点燃海马体以及未受刺激的海马体、新皮质、梨状皮质、内嗅皮质或丘脑区域进行颅内EEG记录。在几乎所有检测到的SRS中,无论是否伴有运动性癫痫发作,均可在两个相应区域观察到伴有同步低电压快速起始的自发性EEG放电。在脑片中进行检查时,碱性人工脑脊液可在延长点燃效应小鼠的海马体CA3区、梨状皮质和内嗅皮质区域诱发癫痫样放电,但在对照小鼠中则不会。总之,这些体内和体外观察结果表明,涉及宏观网络的癫痫活动可能在前脑区域产生同步放电,并在海马体点燃效应的小鼠中引发SRS。