Pitkänen Asla, Sutula Thomas P
Epilepsy Research Laboratory, A I Virtanen Institute for Molecular Sciences, University of Kuopio, and Department of Neurology, Kuopio University Hospital, Kuopio, Finland.
Lancet Neurol. 2002 Jul;1(3):173-81. doi: 10.1016/s1474-4422(02)00073-x.
During the past decade, it has become apparent that neural circuits undergo activity-dependent reorganisation. In pathological disorders with recurring episodes of excessive neural activity, such as temporal-lobe epilepsy, brain circuits can undergo continual remodelling. For clinical practice, seizure-induced remodelling implies that after a diagnosis of epilepsy, recurring seizures can cause continuing neural reorganisation and potentially contribute to progressive severity of the epilepsy and to cognitive and behavioural consequences. The alterations induced by seizures include neuronal death and birth, axonal and dendritic sprouting, gliosis, molecular reorganisation of membrane and extracellular-matrix proteins, and intermediates involved in cellular homoeostasis. These changes are influenced by genetic background and seizure type, thus identification of genetic risk factors should be a priority. Therapeutic modification of seizure-induced molecular and cellular responses offers new opportunities for intervention beyond seizure suppression.
在过去十年中,神经回路会发生依赖于活动的重组这一点已变得很明显。在患有反复出现过度神经活动发作的病理疾病中,如颞叶癫痫,脑回路会经历持续重塑。对于临床实践而言,癫痫发作引起的重塑意味着在癫痫诊断之后,反复的癫痫发作会导致持续的神经重组,并可能导致癫痫病情逐渐加重以及产生认知和行为后果。癫痫发作引起的改变包括神经元死亡和新生、轴突和树突的发芽、胶质增生、膜和细胞外基质蛋白的分子重组以及参与细胞稳态的中间产物。这些变化受遗传背景和癫痫发作类型的影响,因此识别遗传风险因素应是首要任务。对癫痫发作引起的分子和细胞反应进行治疗性调节为除抑制癫痫发作之外的干预提供了新机会。