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Untangling Basal Ganglia Network Dynamics and Function: Role of Dopamine Depletion and Inhibition Investigated in a Spiking Network Model

机译:解开基底神经节网络的动力学和功能:研究多巴胺的消耗和抑制作用在尖峰网络模型中。

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摘要

The basal ganglia are a crucial brain system for behavioral selection, and their function is disturbed in Parkinson’s disease (PD), where neurons exhibit inappropriate synchronization and oscillations. We present a spiking neural model of basal ganglia including plausible details on synaptic dynamics, connectivity patterns, neuron behavior, and dopamine effects. Recordings of neuronal activity in the subthalamic nucleus and Type A (TA; arkypallidal) and Type I (TI; prototypical) neurons in globus pallidus externa were used to validate the model. Simulation experiments predict that both local inhibition in striatum and the existence of an indirect pathway are important for basal ganglia to function properly over a large range of cortical drives. The dopamine depletion–induced increase of AMPA efficacy in corticostriatal synapses to medium spiny neurons (MSNs) with dopamine receptor D2 synapses (CTX-MSN D2) and the reduction of MSN lateral connectivity (MSN–MSN) were found to contribute significantly to the enhanced synchrony and oscillations seen in PD. Additionally, reversing the dopamine depletion–induced changes to CTX–MSN D1, CTX–MSN D2, TA–MSN, and MSN–MSN couplings could improve or restore basal ganglia action selection ability. In summary, we found multiple changes of parameters for synaptic efficacy and neural excitability that could improve action selection ability and at the same time reduce oscillations. Identification of such targets could potentially generate ideas for treatments of PD and increase our understanding of the relation between network dynamics and network function.
机译:基底神经节是行为选择的关键大脑系统,其功能在帕金森氏病(PD)中受到干扰,在帕金森氏病中,神经元表现出不适当的同步和振荡。我们提出了一个基础神经节的尖刺神经模型,包括有关突触动力学,连接模式,神经元行为和多巴胺效应的合理细节。记录下丘脑下核和苍白球外部的A型(TA;侧柏)和I型(TI;原型)神经元的神经元活动,以验证该模型。模拟实验预测纹状体中的局部抑制和间接途径的存在对于基底神经节在大范围的皮质驱动器中正常起作用都是重要的。发现多巴胺引起的皮质上皮突触中枢棘突神经元(MSNs)和多巴胺受体D2突触(CTX-MSN D2)的AMPA效力增加,以及MSN侧向连接性(MSN–MSN)的降低PD中出现同步和振荡。此外,逆转多巴胺消耗引起的CTX–MSN D1,CTX–MSN D2,TA–MSN和MSN–MSN偶联变化可以改善或恢复基底神经节动作选择能力。总之,我们发现了突触功效和神经兴奋性参数的多个变化,这些变化可以提高动作选择能力,同时减少振荡。识别此类目标可能会产生治疗PD的想法,并加深我们对网络动力学与网络功能之间关系的理解。

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