Mariia Popova, Arnaud Messé, Alessandro Gulberti, Christian Gerloff, Monika Pötter-Nerger, Claus C Hilgetag
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引用次数: 0
摘要
目前治疗帕金森病(PD)的方法在缓解步态冻结(FoG)方面疗效有限。在这种情况下,眼下核(STN)和黑质网状旁(SNr)同时进行深部脑刺激(DBS)被认为是一种潜在的治疗方法。然而,这种方法的机制尚不清楚。虽然目前的理论依据是基于网络的假说,即加强脑干运动区的抑制以促进步态运动程序的释放,但目前仍不清楚两个相互连接的基底神经节核团同时进行高频 DBS 会如何影响大规模的皮质-皮质下网络活动。在此,我们使用神经兴奋的基本模型--易感-兴奋-难复(SER)模型,以小鼠大脑连接图谱为基础,比较不同刺激模式对 FoG 基础网络的影响。我们开发了一个基于网络的计算框架,通过对健康、帕金森病和 DBS 状态下大脑吸引子动态的详尽分析来比较皮层下 DBS 靶点。我们的研究表明,就 FoG 网络中尖峰传播流的正常化而言,STN+SNr DBS 组合优于 STN DBS。该框架旨在从机理上理解 DBS 的网络效应,并可进一步应用于基于扰动的脑疾病疗法。
The effect of deep brain stimulation on cortico-subcortical networks in Parkinson's disease patients with freezing of gait: Exhaustive exploration of a basic model.
Current treatments of Parkinson's disease (PD) have limited efficacy in alleviating freezing of gait (FoG). In this context, concomitant deep brain stimulation (DBS) of the subthalamic nucleus (STN) and the substantia nigra pars reticulata (SNr) has been suggested as a potential therapeutic approach. However, the mechanisms underlying this approach are unknown. While the current rationale relies on network-based hypotheses of intensified disinhibition of brainstem locomotor areas to facilitate the release of gait motor programs, it is still unclear how simultaneous high-frequency DBS in two interconnected basal ganglia nuclei affects large-scale cortico-subcortical network activity. Here, we use a basic model of neural excitation, the susceptible-excited-refractory (SER) model, to compare effects of different stimulation modes of the network underlying FoG based on the mouse brain connectivity atlas. We develop a network-based computational framework to compare subcortical DBS targets through exhaustive analysis of the brain attractor dynamics in the healthy, PD, and DBS states. We show that combined STN+SNr DBS outperforms STN DBS in terms of the normalization of spike propagation flow in the FoG network. The framework aims to move toward a mechanistic understanding of the network effects of DBS and may be applicable to further perturbation-based therapies of brain disorders.