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大规模脑癫痫模型:动力学与连接组学的结合。

Large scale brain models of epilepsy: dynamics meets connectomics.

机构信息

King's College London, Institute of Psychiatry, De Crespigny Park, London SE5 8AF, UK.

出版信息

J Neurol Neurosurg Psychiatry. 2012 Dec;83(12):1238-48. doi: 10.1136/jnnp-2011-301944. Epub 2012 Aug 23.

Abstract

The brain is in a constant state of dynamic change, for example switching between cognitive and behavioural tasks, and between wakefulness and sleep. The brains of people with epilepsy have additional features to their dynamic repertoire, particularly the paroxysmal occurrence of seizures. Substantial effort over decades has produced a detailed description of many human epilepsies and of specific seizure types; in some instances there are known causes, sometimes highly specific such as single gene mutations, but the mechanisms of seizure onset and termination are not known. A large number of in vivo animal models and in vitro models based on animal tissues can generate seizures and seizure-like phenomena. Although in some instances there is much known about the mechanism of seizure onset and termination, across the range of models there is a bewildering range of mechanisms. There is a pressing need to bridge the gap between microscale mechanisms in experimental models and mechanisms of human epilepsies. Computational models of epilepsy have advanced rapidly, allowing dynamic mechanisms to be revealed in a computer model that can then be tested in biological systems. These models are typically simplified, leaving a need to scale up these models to the large scale brain networks in which seizures become manifest. The emerging science of connectomics provides an approach to understanding the large scale brain networks in which normal and abnormal brain functions operate. The stage is now set to couple dynamics with connectomics, to reveal the abnormal dynamics of brain networks which allow seizures to occur.

摘要

大脑处于不断变化的动态状态,例如在认知和行为任务之间切换,以及在清醒和睡眠之间切换。癫痫患者的大脑具有其动态特征之外的额外特征,特别是阵发性发作。数十年来,人们付出了巨大的努力,对许多人类癫痫和特定的发作类型进行了详细描述;在某些情况下,已知有特定的原因,有时是高度特异性的,如单基因突变,但发作的起始和终止机制尚不清楚。大量基于动物组织的体内动物模型和体外模型可以引发发作和类似发作的现象。尽管在某些情况下,人们对发作起始和终止的机制有了很多了解,但在各种模型中,存在着令人眼花缭乱的多种机制。迫切需要弥合实验模型中的微观机制与人类癫痫机制之间的差距。癫痫的计算模型发展迅速,允许在计算机模型中揭示动态机制,然后可以在生物系统中对其进行测试。这些模型通常是简化的,需要将这些模型扩展到发作表现出来的大型大脑网络。连接组学这一新兴科学为理解正常和异常大脑功能运作的大规模大脑网络提供了一种方法。现在已经为将动力学与连接组学相结合奠定了基础,以揭示允许发作发生的大脑网络的异常动力学。

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