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可塑性调制的癫痫发作动力学用于终止现实神经元模型中的癫痫发作。

Plasticity-modulated seizure dynamics for seizure termination in realistic neuronal models.

机构信息

Stichting Epilepsie Instellingen Nederland, Achterweg 5, 2103 SW Heemstede, The Netherlands.

出版信息

J Neural Eng. 2011 Aug;8(4):046027. doi: 10.1088/1741-2560/8/4/046027. Epub 2011 Jul 6.

Abstract

In previous studies we showed that autonomous absence seizure generation and termination can be explained by realistic neuronal models eliciting bi-stable dynamics. In these models epileptic seizures are triggered either by external stimuli (reflex epilepsies) or by internal fluctuations. This scenario predicts exponential distributions of the duration of the seizures and of the inter-ictal intervals. These predictions were validated in rat models of absence epilepsy, as well as in a few human cases. Nonetheless, deviations from the predictions with respect to seizure duration distributions remained unexplained. The objective of the present work is to implement a simple but realistic computational model of a neuronal network including synaptic plasticity and ionic current dynamics and to explore the dynamics of the model with special emphasis on the distributions of seizure and inter-ictal period durations. We use as a basis our lumped model of cortical neuronal circuits. Here we introduce 'activity dependent' parameters, namely post-synaptic voltage-dependent plasticity, as well as a voltage-dependent hyperpolarization-activated current driven by slow and fast activation conductances. We examine the distributions of the durations of the seizure-like model activity and the normal activity, described respectively by the limit cycle and the steady state in the dynamics. We use a parametric γ-distribution fit as a quantifier. Our results show that autonomous, activity-dependent membrane processes can account for experimentally obtained statistical distributions of seizure durations, which were not explainable using the previous model. The activity-dependent membrane processes that display the strongest effect in accounting for these distributions are the hyperpolarization-dependent cationic (I(h)) current and the GABAa plastic dynamics. Plastic synapses (NMDA-type) in the interneuron population show only a minor effect. The inter-ictal statistics retain their consistency with the experimental data and the previous model.

摘要

在之前的研究中,我们表明自主失神发作的产生和终止可以用引发双稳态动力学的现实神经元模型来解释。在这些模型中,癫痫发作要么由外部刺激引发(反射性癫痫),要么由内部波动引发。这种情况预测了发作持续时间和发作间期的指数分布。这些预测在大鼠失神癫痫模型中得到了验证,在少数人类病例中也得到了验证。尽管如此,与发作持续时间分布有关的偏离预测仍未得到解释。本工作的目的是实现一个包括突触可塑性和离子电流动力学的简单但现实的神经元网络计算模型,并特别强调模型的动力学,探索发作和发作间期持续时间分布。我们以皮质神经元回路的集中模型为基础。在这里,我们引入了“活动依赖”参数,即突触后电压依赖性可塑性,以及由慢和快激活电导驱动的电压依赖性超极化激活电流。我们检查了类似发作的模型活动和正常活动的持续时间分布,分别由动力学中的极限环和稳态描述。我们使用参数γ分布拟合作为量化器。我们的结果表明,自主的、活动依赖性的膜过程可以解释实验获得的发作持续时间的统计分布,而使用之前的模型无法解释这些分布。在解释这些分布方面影响最大的活动依赖性膜过程是去极化依赖性阳离子(I(h))电流和 GABAa 可塑性动力学。中间神经元群体中的可塑性突触(NMDA 型)仅显示出较小的影响。发作间期的统计数据仍然与实验数据和之前的模型一致。

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