Fish D R, Sawyers D, Smith S J, Allen P J, Murray N M, Marsden C D
University Department of Clinical Neurology, National Hospitals for Neurology and Neurosurgery, London, UK.
J Neurol Neurosurg Psychiatry. 1991 Feb;54(2):140-4. doi: 10.1136/jnnp.54.2.140.
The maintenance of axial atonia during REM sleep was monitored in 14 patients with primary torsion dystonia, 10 patients with secondary torsion dystonia, and 10 normal subjects using submental EMG and video EEG telemetry. The excitability of the corticospinal tract during REM sleep was also assessed using scalp magnetic stimulation in seven patients and three controls. During REM sleep dystonic patients had well maintained atonia evidenced by infrequent bursts of submental activity, no episodes of complex semi-purposeful behaviour and reduced motor responses to magnetic stimulation. These findings suggest that the inhibitory centres in the region of the locus coeruleus and their descending pathways to the spinal alpha motor neurons are intact in torsion dystonia.
采用颏下肌肌电图和视频脑电图遥测技术,对14例原发性扭转性肌张力障碍患者、10例继发性扭转性肌张力障碍患者和10名正常受试者在快速眼动睡眠期间的轴性肌张力缺失维持情况进行了监测。还通过头皮磁刺激对7例患者和3名对照者在快速眼动睡眠期间皮质脊髓束的兴奋性进行了评估。在快速眼动睡眠期间,肌张力障碍患者的肌张力缺失维持良好,表现为颏下肌活动偶尔爆发、无复杂的半目的性行为发作以及对磁刺激的运动反应减弱。这些发现表明,在扭转性肌张力障碍中,蓝斑区域的抑制性中枢及其向脊髓α运动神经元的下行通路是完整的。