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药物诱导的迟发性运动障碍患者运动皮层兴奋和抑制募集的变化。

Changes in recruitment of motor cortex excitation and inhibition in patients with drug-induced tardive syndromes.

机构信息

Department of Neuropsychiatry, Faculty of Medicine, Assiut University, Assiut, Egypt; Department of Neuropsychiatry, Faculty of Medicine, Aswan University, Aswan, Egypt.

Department of Neuropsychiatry, Faculty of Medicine, Aswan University, Aswan, Egypt.

出版信息

Neurophysiol Clin. 2019 Feb;49(1):33-40. doi: 10.1016/j.neucli.2018.10.001. Epub 2018 Oct 23.


DOI:10.1016/j.neucli.2018.10.001
PMID:30366858
Abstract

OBJECTIVES: It has recently been suggested that drug-induced tardive syndromes (TS) might be due to maladaptive plasticity, which increases motor excitability in cerebral cortex and basal ganglia. In order to test this hypothesis, we performed the first measurements of cortical excitability in TS. METHODS: Motor cortex excitability was examined using transcranial magnetic stimulation (TMS) in 22 TS patients and compared with that in 20 age and sex-matched healthy individuals. Resting and active motor threshold (RMT, AMT) and input-output curves (I/O curves) assessed corticospinal excitability. The duration of the contralateral silent period (cSP) at a range of stimulation intensities and ipsilateral silent period (iSP) were used as measures of inhibition. RESULTS: There were no significant differences in RMT and AMT between patients and controls, although the input-output curves were significantly steeper in patients. The cSP (at different stimulus intensities) and iSP were both longer in the patients compared to the control group. However, most of this difference could be accounted for by increased recruitment of motor evoked potentials (MEPs) in patients. CONCLUSION: TS is characterized by hyperexcitability of corticospinal output that might contribute to the lack of selectivity in muscle recruitment and contribute to excess involuntary movement. The findings are opposite to those in naturally-occurring hyperkinesia such as Sydenham's and Huntington's chorea, suggesting a fundamental difference in the pathophysiology.

摘要

目的:最近有人提出,药物引起的迟发性运动障碍(TS)可能是由于适应不良的可塑性所致,这种可塑性增加了大脑皮层和基底节的运动兴奋性。为了验证这一假设,我们首次对 TS 患者的皮质兴奋性进行了测量。

方法:使用经颅磁刺激(TMS)检查 22 名 TS 患者和 20 名年龄和性别匹配的健康个体的运动皮质兴奋性,并将其与后者进行比较。静息和主动运动阈值(RMT、AMT)和输入-输出曲线(I/O 曲线)评估皮质脊髓兴奋性。在一系列刺激强度下测量对侧静息期(cSP)和同侧静息期(iSP)的持续时间,作为抑制的测量指标。

结果:患者和对照组之间的 RMT 和 AMT 没有显著差异,尽管患者的输入-输出曲线明显陡峭。与对照组相比,患者的 cSP(在不同刺激强度下)和 iSP 均较长。然而,这种差异的大部分可以通过患者运动诱发电位(MEP)的募集增加来解释。

结论:TS 的特征是皮质脊髓输出的过度兴奋性,这可能导致肌肉募集缺乏选择性,并导致过度的不自主运动。这些发现与自然发生的运动过度(如舞蹈病和亨廷顿病)相反,表明其病理生理学存在根本差异。

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