Cellular and molecular mechanisms of epilepsy in the human brain

被引:150
作者
Avoli, M
Louvel, J
Pumain, R
Köhling, R
机构
[1] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Neurol, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Neurosurg, Montreal, PQ H3A 2B4, Canada
[4] McGill Univ, Dept Physiol, Montreal, PQ H3A 2B4, Canada
[5] Univ Roma La Sapienza, Dipartimento Fisiol Umana & Farmacol, I-00185 Rome, Italy
[6] INSERM, U109, Ctr Paul Broca, F-75014 Paris, France
[7] Univ Rostock, Inst Physiol, D-18055 Rostock, Germany
关键词
epilepsy; pathophysiology; GABA; temporal lobe; focal dysplasia; electrophysiology; histology;
D O I
10.1016/j.pneurobio.2005.09.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Animal models have provided invaluable data for identifying the pathogenesis of epileptic disorders. Clearly, the relevance of these experimental findings would be strengthened by the demonstration that similar fundamental mechanisms are at work in the human epileptic brain. Epilepsy surgery has indeed opened the possibility to directly study the functional properties of human brain tissue in vitro, and to analyze the mechanisms underlying seizures and epileptogenesis. Here, we summarize the findings obtained over the last 40 years from electrophysiological, histochemical and molecular experiments made with the human brain tissue. In particular, this review will focus on (i) the synaptic and nonsynaptic properties of neocortical neurons along with their ability to Produce synchronous activity; (ii) the anatomical and functional alterations that characterize limbic structures in patients presenting with mesial temporal lobe epilepsy; (iii) the issue of antiepileptic drug action and resistance; and (iv) the pathophysiology of seizure genesis in Taylor's type focal cortical dysplasia. Finally, we will address some of the problems that are inherent to this type of experimental approach, in particular the lack of proper controls and possible strategies to obviate this limitation. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 200
页数:35
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