Frequency- and layer-specific effects of high-frequency STN stimulation on mouse motor cortical areas in vivo.

IF 2.9 2区 医学 Q2 NEUROSCIENCES
Svenja L Kreis, Gabriel Gonzalez-Escamilla, Daniela Mirzac, Muthuraman Muthuraman, Heiko J Luhmann, Sergiu Groppa
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Abstract

High-frequency deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective evidence-based therapy for Parkinson's disease; however, its effects on the motor network are unclear. In anesthetized mice we studied the layer (L)- and frequency-specific effects of DBS on the connectivity between STN and rostral and caudal forelimb area (RFA and CFA) layers, the respective homologs to human premotor and motor cortex. Multi-site extracellular recordings served to quantify local field potential-driven activity at rest and during burst STN stimulation at multiple stimulation-frequencies for 10 min. The combination of frequency-specific coherence and information flow dynamics from effective connectivity (EC) demonstrated that 160 Hz STN stimulation increases the high-γ power in RFA and CFA. Additionally, 160 Hz STN stimulation reduced the β- and high γ-frequency coherence between RFA, CFA, and STN, as well as the EC from STN towards RFA and CFA, but no change in the connectivity from cortex towards STN was attested, demonstrating hyperdirect pathway activation. Our work provides empirical insights into the mechanisms of action of DBS, which represent an important basis for the further development of this therapy.

高频STN刺激对小鼠体内运动皮质区的频率和层特异性影响。
丘脑下核高频深部脑刺激(DBS)是治疗帕金森病的有效循证疗法;然而,它对运动网络的影响尚不清楚。在麻醉小鼠中,我们研究了DBS对STN与吻侧和尾侧前肢区(RFA和CFA)层之间连接的层(L)和频率特异性影响,这两个层分别与人类的运动前皮层和运动皮层相似。多位点细胞外记录用于量化静息和脉冲STN刺激期间10分钟的局部场电位驱动活动。频率特异性相干性和有效连通性(EC)信息流动力学的结合表明,160 Hz STN刺激增加了RFA和CFA的高γ功率。此外,160 Hz STN刺激降低了RFA、CFA和STN之间的β-和高γ-频率相干性,以及STN对RFA和CFA的EC,但皮层对STN的连通性没有改变,证明了超直接通路激活。我们的工作为DBS的作用机制提供了经验见解,这为该疗法的进一步发展奠定了重要基础。
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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
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