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不同的机制可能在特发性肌张力障碍中产生持续性高渗性和节律性爆发性肌肉活动。

Different mechanisms may generate sustained hypertonic and rhythmic bursting muscle activity in idiopathic dystonia.

作者信息

Liu Xuguang, Yianni John, Wang Shouyan, Bain Peter G, Stein John F, Aziz Tipu Z

机构信息

The Movement Disorders and Neurostimulation Unit, Charing Cross Hospital and Division of Neuroscience and Mental Health, Imperial College London, 11L15 East Block, Charing Cross Hospital, Fulham Palace Road, London W6 8RF, UK.

出版信息

Exp Neurol. 2006 Mar;198(1):204-13. doi: 10.1016/j.expneurol.2005.11.018. Epub 2006 Jan 10.

DOI:10.1016/j.expneurol.2005.11.018
PMID:16410002
Abstract

Despite that deep brain stimulation (DBS) of the globus pallidus internus (GPi) is emerging as the favored intervention for patients with medically intractable dystonia, the pathophysiological mechanisms of dystonia are largely unclear. In eight patients with primary dystonia who were treated with bilateral chronic pallidal stimulation, we correlated symptom-related electromyogram (EMG) activity of the most affected muscles with the local field potentials (LFPs) recorded from the globus pallidus electrodes. In 5 dystonic patients with mobile involuntary movements, rhythmic EMG bursts in the contralateral muscles were coherent with the oscillations in the pallidal LFPs at the burst frequency. In contrast, no significant coherence was seen between EMG and LFPs either for the sustained activity separated out from the compound EMGs in those 5 cases, or in the EMGs in 3 other cases without mobile involuntary movements and rhythmic EMG bursts. In comparison with the resting condition, in both active and passive movements, significant modulation in the GPi LFPs was seen in the range of 8-16 Hz. The finding of significant coherence between GPi oscillations and rhythmic EMG bursts but not sustained tonic EMG activity suggests that the synchronized pallidal activity may be directly related to the rhythmic involuntary movements. In contrast, the sustained hypertonic muscle activity may be represented by less synchronized activity in the pallidum. Thus, the pallidum may play different roles in generating different components of the dystonic symptom complex.

摘要

尽管内侧苍白球(GPi)的深部脑刺激(DBS)正在成为药物难治性肌张力障碍患者的首选干预措施,但肌张力障碍的病理生理机制在很大程度上尚不清楚。在8例接受双侧慢性苍白球刺激治疗的原发性肌张力障碍患者中,我们将最受影响肌肉的症状相关肌电图(EMG)活动与从苍白球电极记录的局部场电位(LFP)进行了关联。在5例有可移动性不自主运动的肌张力障碍患者中,对侧肌肉的节律性EMG爆发与苍白球LFP在爆发频率处的振荡具有相关性。相比之下,在这5例患者中,从复合EMG中分离出的持续活动的EMG与LFP之间,以及在另外3例没有可移动性不自主运动和节律性EMG爆发的患者的EMG中,均未观察到显著的相关性。与静息状态相比,在主动和被动运动中,苍白球LFP在8-16Hz范围内均出现了显著调制。苍白球振荡与节律性EMG爆发之间存在显著相关性,但与持续的紧张性EMG活动无关,这一发现表明,苍白球的同步活动可能与节律性不自主运动直接相关。相比之下,持续的高张性肌肉活动可能由苍白球中同步性较低的活动所代表。因此,苍白球在肌张力障碍症状复合体的不同组成部分的产生中可能发挥不同作用。

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