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人类丘脑底核中β和高频活动的耦合可能是帕金森病的一种病理生理机制。

Coupling between beta and high-frequency activity in the human subthalamic nucleus may be a pathophysiological mechanism in Parkinson's disease.

机构信息

Neuroscience Area, Centro de Investigación Médica Aplicada, Universidad de Navarra, 31008 Pamplona, Spain.

出版信息

J Neurosci. 2010 May 12;30(19):6667-77. doi: 10.1523/JNEUROSCI.5459-09.2010.

Abstract

In Parkinson's disease (PD), the oscillatory activity recorded from the basal ganglia shows dopamine-dependent changes. In the "off" parkinsonian motor state, there is prominent activity in the beta band (12-30 Hz) that is mostly attenuated after dopaminergic therapy ("on" medication state). The on state is also characterized by activity in the gamma (60-80 Hz) and high-frequency (300 Hz) bands that is modulated by movement. We recorded local field potentials from a group of 15 PD patients (three females) treated with bilateral deep brain stimulation of the subthalamic nucleus, using a high sampling rate (2 kHz) and filters suitable to study high-frequency activity (0.3-1000 Hz). We observed high-frequency oscillations (HFOs) in both the off and on motor states. In the off state, the amplitude of the HFOs was coupled to the phase of the abnormal beta activity. The beta-coupled HFOs showed little or even negative movement-related changes in amplitude. Moreover, the degree of movement-related modulation of the HFOs correlated negatively with the rigidity/bradykinesia scores. In the on motor state, the HFOs were liberated from this beta coupling, and they displayed marked movement-related amplitude modulation. Cross-frequency interactions between the phase of slow activities and the amplitude of fast frequencies have been attributed an important role in information processing in cortical structures. Our findings suggest that nonlinear coupling between frequencies may not only be a physiological mechanism (as shown previously) but also that it may participate in the pathophysiology of parkinsonism.

摘要

在帕金森病(PD)中,从基底神经节记录到的振荡活动显示出多巴胺依赖性变化。在“关”期帕金森运动状态下,β频段(12-30 Hz)有明显的活动,在多巴胺能治疗后(“开”药状态)大多减弱。“开”期还以γ(60-80 Hz)和高频(300 Hz)频段的活动为特征,这些活动受运动调节。我们使用高采样率(2 kHz)和适合研究高频活动(0.3-1000 Hz)的滤波器,从 15 名接受双侧丘脑底核深部脑刺激治疗的 PD 患者中记录局部场电位。我们观察到在“关”和“开”运动状态下均存在高频振荡(HFOs)。在“关”期,HFOs 的幅度与异常β活动的相位耦合。β耦合的 HFOs 表现出振幅上的运动相关性变化很小,甚至为负。此外,HFOs 的运动相关性调制程度与僵直/运动迟缓评分呈负相关。在“开”期运动状态下,HFOs 从这种β耦合中解放出来,并显示出明显的运动相关幅度调制。慢活动相位和快频率幅度之间的交叉频率相互作用被认为在皮质结构的信息处理中起着重要作用。我们的发现表明,频率之间的非线性耦合不仅可能是一种生理机制(如前所述),而且可能参与帕金森病的病理生理学。

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