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癫痫的神经生物学

The neurobiology of epilepsy.

作者信息

Scharfman Helen E

机构信息

Nathan Kline Institute for Psychiatric Research, 140 Old Orangeburg Road, Building 35, Orangetown, NY 10962, USA.

出版信息

Curr Neurol Neurosci Rep. 2007 Jul;7(4):348-54. doi: 10.1007/s11910-007-0053-z.

Abstract

Epilepsy is a complex disease with diverse clinical characteristics that preclude a singular mechanism. One way to gain insight into potential mechanisms is to reduce the features of epilepsy to its basic components: seizures, epileptogenesis, and the state of recurrent unprovoked seizures that defines epilepsy itself. A common way to explain seizures in a normal individual is that a disruption has occurred in the normal balance of excitation and inhibition. The fact that multiple mechanisms exist is not surprising given the varied ways the normal nervous system controls this balance. In contrast, understanding seizures in the brain of an individual with epilepsy is more difficult because seizures are typically superimposed on an altered nervous system. The different environment includes diverse changes, making mechanistic predictions a challenge. Understanding the mechanisms of seizures in an individual with epilepsy is also more complex than understanding the mechanisms of seizures in a normal individual because epilepsy is not necessarily a static condition but can continue to evolve over the lifespan. Using temporal lobe epilepsy as an example, it is clear that genes, developmental mechanisms, and neuronal plasticity play major roles in creating a state of underlying hyperexcitability. However, the critical control points for the emergence of chronic seizures in temporal lobe epilepsy, as well as their persistence, frequency, and severity, are questions that remain unresolved.

摘要

癫痫是一种具有多样临床特征的复杂疾病,不存在单一的发病机制。深入了解潜在机制的一种方法是将癫痫的特征分解为其基本组成部分:发作、癫痫发生以及定义癫痫本身的反复无诱因发作状态。解释正常个体发作的一种常见方式是,正常的兴奋与抑制平衡受到了破坏。鉴于正常神经系统控制这种平衡的方式多种多样,存在多种机制这一事实并不令人惊讶。相比之下,理解癫痫患者大脑中的发作情况更为困难,因为发作通常叠加在已改变的神经系统之上。这种不同的环境包含各种变化,使得对发病机制的预测成为一项挑战。理解癫痫患者发作的机制也比理解正常个体发作的机制更为复杂,因为癫痫不一定是一种静态疾病,而是可能在整个生命周期中持续演变。以颞叶癫痫为例,很明显基因、发育机制和神经元可塑性在产生潜在的过度兴奋状态中起主要作用。然而,颞叶癫痫中慢性发作出现的关键控制点,以及它们的持续时间、频率和严重程度,仍然是尚未解决的问题。

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