Yan Han, Wang Jin
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, P.R.China.
Department of Chemistry and Physics, State University of New York at Stony Brook, Stony Brook, New York, United States of America.
PLoS One. 2017 Mar 28;12(3):e0174364. doi: 10.1371/journal.pone.0174364. eCollection 2017.
The basal ganglia neural circuit plays an important role in motor control. Despite the significant efforts, the understanding of the principles and underlying mechanisms of this modulatory circuit and the emergence of abnormal synchronized oscillations in movement disorders is still challenging. Dopamine loss has been proved to be responsible for Parkinson's disease. We quantitatively described the dynamics of the basal ganglia-thalamo-cortical circuit in Parkinson's disease in terms of the emergence of both abnormal firing rates and firing patterns in the circuit. We developed a potential landscape and flux framework for exploring the modulatory circuit. The driving force of the circuit can be decomposed into a gradient of the potential, which is associated with the steady-state probability distributions, and the curl probability flux term. We uncovered the underlying potential landscape as a Mexican hat-shape closed ring valley where abnormal oscillations emerge due to dopamine depletion. We quantified the global stability of the network through the topography of the landscape in terms of the barrier height, which is defined as the potential difference between the maximum potential inside the ring and the minimum potential along the ring. Both a higher barrier and a larger flux originated from detailed balance breaking result in more stable oscillations. Meanwhile, more energy is consumed to support the increasing flux. Global sensitivity analysis on the landscape topography and flux indicates how changes in underlying neural network regulatory wirings and external inputs influence the dynamics of the system. We validated two of the main hypotheses(direct inhibition hypothesis and output activation hypothesis) on the therapeutic mechanism of deep brain stimulation (DBS). We found GPe appears to be another effective stimulated target for DBS besides GPi and STN. Our approach provides a general way to quantitatively explore neural networks and may help for uncovering more efficacious therapies for movement disorders.
基底神经节神经回路在运动控制中起着重要作用。尽管付出了巨大努力,但对该调节回路的原理和潜在机制以及运动障碍中异常同步振荡的出现的理解仍然具有挑战性。多巴胺缺失已被证明是帕金森病的病因。我们从回路中异常放电率和放电模式的出现方面,定量描述了帕金森病中基底神经节 - 丘脑 - 皮质回路的动力学。我们开发了一种用于探索调节回路的势场和通量框架。回路的驱动力可以分解为与稳态概率分布相关的势梯度和旋度概率通量项。我们发现潜在的势场是一个墨西哥帽形状的闭环山谷,由于多巴胺耗竭会出现异常振荡。我们通过势场的地形,根据势垒高度量化了网络的全局稳定性,势垒高度定义为环内最大势与沿环的最小势之间的势差。更高的势垒和源于详细平衡破坏的更大通量都会导致更稳定的振荡。同时,需要消耗更多能量来支持不断增加的通量。对势场地形和通量的全局敏感性分析表明,底层神经网络调节布线和外部输入的变化如何影响系统的动力学。我们验证了关于深部脑刺激(DBS)治疗机制的两个主要假设(直接抑制假设和输出激活假设)。我们发现除了苍白球内侧核(GPi)和丘脑底核(STN)之外,苍白球外侧核(GPe)似乎是DBS的另一个有效刺激靶点。我们的方法提供了一种定量探索神经网络的通用方法,可能有助于发现针对运动障碍更有效的治疗方法。