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随着帕金森病严重程度的增加,苍白球振荡频率和耦合的调制。

Modulations in oscillatory frequency and coupling in globus pallidus with increasing parkinsonian severity.

作者信息

Connolly Allison T, Jensen Alicia L, Bello Edward M, Netoff Theoden I, Baker Kenneth B, Johnson Matthew D, Vitek Jerrold L

机构信息

Department of Biomedical Engineering and.

Department of Neurology, University of Minnesota, Minneapolis, Minnesota 55455 and.

出版信息

J Neurosci. 2015 Apr 15;35(15):6231-40. doi: 10.1523/JNEUROSCI.4137-14.2015.

Abstract

While beta oscillations often occur within the parkinsonian basal ganglia, how these oscillations emerge from a naive state and change with disease severity is not clear. To address this question, a progressive, nonhuman primate model of Parkinson's disease was developed using staged injections of MPTP. Within each parkinsonian state (naive, mild, moderate, and severe), spontaneous local field potentials were recorded throughout the sensorimotor globus pallidus. In the naive state, beta oscillations (11-32 Hz) occurred in half of the recordings, indicating spontaneous beta oscillations in globus pallidus are not pathognomonic. Mild and moderate states were characterized by a narrower distribution of beta frequencies that shifted toward the 8-15 Hz range. Additionally, coupling between the phase of beta and the amplitude of high-frequency oscillations (256-362 Hz) emerged in the mild state and increased with severity. These findings provide a novel mechanistic framework to understand how progressive loss of dopamine translates into abnormal information processing in the pallidum through alterations in oscillatory activity. The results suggest that rather than the emergence of oscillatory activity in one frequency spectrum or the other, parkinsonian motor signs may relate more to the development of altered coupling across multiple frequency spectrums.

摘要

虽然β振荡经常出现在帕金森病的基底神经节内,但这些振荡如何从初始状态出现并随疾病严重程度变化尚不清楚。为了解决这个问题,使用分期注射MPTP建立了一种进行性的帕金森病非人灵长类动物模型。在每个帕金森病状态(初始、轻度、中度和重度)下,在整个感觉运动苍白球记录自发局部场电位。在初始状态下,一半的记录中出现了β振荡(11 - 32赫兹),这表明苍白球中的自发β振荡并非帕金森病所特有的。轻度和中度状态的特征是β频率分布变窄,并向8 - 15赫兹范围偏移。此外,β相位与高频振荡(256 - 362赫兹)幅度之间的耦合在轻度状态下出现,并随严重程度增加。这些发现提供了一个新的机制框架,以理解多巴胺的逐渐丧失如何通过振荡活动的改变转化为苍白球中异常的信息处理。结果表明,帕金森病的运动症状可能更多地与多个频谱间耦合改变的发展有关,而不是某一个频谱中振荡活动的出现。

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