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Simulation Study of Intermittent Responses of Neuronal Populations to Axonal High-Frequency Stimulation

机译:神经元群体对轴突高频刺激间歇性反应的模拟研究

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Deep brain stimulation (DBS) have shown a promising future for treating various brain disorders. Studies have indicated that the high frequency stimulation (HFS) used in DBS could cause a partial block in axons thereby attenuating the responses of axon fibers to the pulses of HFS. The attenuated response of axons might play a desynchronization role in modulating activity of neuronal populations. To investigate the detail behavior of individual axons under HFS, we created a computational model of neuronal populations including 1250 neurons. Each neuron consisted of a myelinated axon, an axonal initial segment, a soma and dendrites. A 10-s HFS sequence with 100 Hz pulses was applied to the axon layer by a bipolar stimulation electrode. The membrane potentials and the extracellular potassium concentration [K+]o at axons and at somata during the stimulation were investigated. The results showed that the simulation model with a mechanism of potassium accumulation could reproduce the attenuated responses of neuronal populations to persistent axonal HFS in rat experiments. The elevation of [K+]o during HFS resulted in an increase of basic membrane potentials and then generated a depolarization block in the axonal membrane thereby attenuating the responses of neuronal populations. The depolarization block in axons included both complete block (~26%) and intermittent block (~74%), which generated desynchronized firing among axons in fibers and travelled to the cell bodies to induce desynchronized firing in somata. The simulation results may provide important information for revealing the modulation mechanisms of axonal HFS in the therapy of brain stimulation.
机译:深部脑刺激(DBS)已显示出治疗各种脑部疾病的有希望的未来。研究表明,DBS中使用的高频刺激(HFS)可能会导致轴突部分阻塞,从而减弱轴突纤维对HFS脉冲的响应。轴突的减弱的反应可能在调节神经元种群的活动中起去同步作用。为了研究HFS下单个轴突的详细行为,我们创建了包括1250个神经元在内的神经元种群的计算模型。每个神经元由有髓的轴突,轴突的初始节段,躯体和树突组成。通过双极刺激电极将具有100 Hz脉冲的10-s HFS序列施加到轴突层。膜电位和细胞外钾浓度[K + 研究了在刺激过程中轴突和躯体的变化。结果表明,在大鼠实验中,具有钾积累机制的模拟模型可以重现神经元群体对持续性轴突HFS的减弱反应。海拔[K + 在HFS期间,o导致碱性膜电位增加,然后在轴突膜中产生去极化阻滞,从而减弱了神经元群体的反应。轴突中的去极化阻滞包括完全阻滞(〜26%)和间歇性阻滞(〜74%),这会在纤维中的轴突之间产生失同步的放电,并传播到细胞体,从而在躯体中诱导失同步的放电。仿真结果可能为揭示轴突HFS在脑刺激治疗中的调控机制提供重要信息。

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