Time-course of neuronal death in the mouse pilocarpine model of chronic epilepsy using Fluoro-Jade C staining

被引:91
作者
Wang, Lian [1 ,2 ]
Liu, Yong-Hong [1 ,2 ]
Huang, Yuan-Gui [2 ]
Chen, Liang-Wei [1 ]
机构
[1] Fourth Mil Med Univ, Inst Neurosci, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Xijing Hosp, Dept Neurol, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Epilepsy; Status epilepticus; Pilocarpine; Fluoro-Jade C; Neurodegeneration; Apoptosis;
D O I
10.1016/j.brainres.2008.07.097
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Epilepsy is a serious neurological disorder in human beings and the long-term pathological events remain largely obscure. We are interested in elucidating long-term brain injury that may occur in the temporal lobe epilepsy, and time-course of neuronal death was examined in a mouse pilocarpine model of chronic epilepsy by Fluoro-Jade C (FJC) dye that can specifically stain the degenerative neurons in the central nervous system. The FJC stain combined with immunohistochemistry to neuronal nuclear specific protein revealed that pilocarpine-induced status epilepticus (SE) resulted in massive degenerative death of neuronal cells in brains with their dense distribution in the cerebral cortex and hippocampus. The FJC-positive degenerating neurons, most of them also expressed apoptosis signaling molecules such as caspase-9 and activated caspase-3, occur-red at 4h, increased into peak levels at 12h-3d, and then gradually went down at 7d-14d after onset of SE. More interestingly, a large percentage (about 88%) of FJC-positive degenerative neurons were GABAergic as indicated with their immunoreactivity to glutamic acid decarboxylase-67, implying that inhibitory function of GABAergic neural system might by seriously damaged in brains subject to SE attack in this mouse pilocarpine model. Taken together with previous studies, time-course of degenerative neurons in the mouse pilocarpine model by Fluoro-Jade C staining further benefits understanding of long-term brain pathological changes and recurrent seizure mechanism, and may also result in finding the most suitable time-window in therapeutic manipulation of the chronic epilepsy in human beings. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:157 / 167
页数:11
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