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帕金森病丘脑底核中的β 键合高频活动和β 锁定神经元放电。

Beta-coupled high-frequency activity and beta-locked neuronal spiking in the subthalamic nucleus of Parkinson's disease.

机构信息

Surgical Neurology Branch.

Office of the Clinical Director, and Human Motor Control Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Neurosci. 2014 Sep 17;34(38):12816-27. doi: 10.1523/JNEUROSCI.1895-14.2014.

Abstract

Beta frequency (13-30 Hz) oscillatory activity in the subthalamic nucleus (STN) of Parkinson's disease (PD) has been shown to influence the temporal dynamics of high-frequency oscillations (HFOs; 200-500 Hz) and single neurons, potentially compromising the functional flexibility of the motor circuit. We examined these interactions by simultaneously recording both local field potential and single-unit activity from the basal ganglia of 15 patients with PD during deep brain stimulation (DBS) surgery of the bilateral STN. Phase-amplitude coupling (PAC) in the STN was specific to beta phase and HFO amplitude, and this coupling was strongest at the dorsal STN border. We found higher beta-HFO PAC near DBS lead contacts that were clinically effective compared with the remaining non-effective contacts, indicating that PAC may be predictive of response to STN DBS. Neuronal spiking was locked to the phase of 8-30 Hz oscillations, and the spatial topography of spike-phase locking (SPL) was similar to that of PAC. Comparisons of PAC and SPL showed a lack of spatiotemporal correlations. Beta-coupled HFOs and field-locked neurons had different preferred phase angles and did not co-occur within the same cycle of the modulating oscillation. Our findings provide additional support that beta-HFO PAC may be central to the pathophysiology of PD and suggest that field-locked neurons alone are not sufficient for the emergence of beta-coupled HFOs.

摘要

在帕金森病(PD)患者的丘脑底核(STN)中,β频率(13-30 Hz)的振荡活动已被证明会影响高频振荡(HFO;200-500 Hz)和单个神经元的时间动态,可能会损害运动回路的功能灵活性。我们通过在 15 名 PD 患者的双侧 STN 深部脑刺激(DBS)手术期间,同时从基底神经节记录局部场电位和单个单元活动,来检查这些相互作用。STN 中的相位-幅度耦合(PAC)是特定于β相和 HFO 幅度的,这种耦合在 STN 背侧边界最强。我们发现,与其余非有效接触相比,在与临床有效的 DBS 导联接触附近,β-HFO PAC 更高,这表明 PAC 可能是对 STN DBS 反应的预测因素。神经元的尖峰锁定在 8-30 Hz 振荡的相位上,并且尖峰相位锁定(SPL)的空间拓扑结构与 PAC 相似。PAC 和 SPL 的比较表明,不存在时空相关性。β 耦合的 HFO 和场锁定神经元具有不同的首选相位角,并且不会在调制振荡的同一周期内同时出现。我们的研究结果进一步支持β-HFO PAC 可能是 PD 病理生理学的核心,并表明仅场锁定神经元不足以产生β 耦合的 HFO。

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