Eyre J A, Kerr A M, Miller S, O'Sullivan M C, Ramesh V
Department of Child Health, University of Newcastle upon Tyne, United Kingdom.
J Neurol Neurosurg Psychiatry. 1990 Oct;53(10):874-9. doi: 10.1136/jnnp.53.10.874.
The aim of the present study was to investigate the excitability of corticospinal neurons and the integrity of their projections to the alpha motor neurons through the corticospinal tract in subjects of different ages with Rett syndrome. Electromagnetic stimulation of the motor cortex and cervical motor roots was used to evoke motor action potentials in the biceps brachii and hypothenar muscles. The phasic stretch reflex in the biceps brachii was also recorded to study the excitability of spinal alpha motor neurons. Motor cortex stimulation evoked motor action potentials at low threshold and with abnormally short latencies and prolonged durations. In contrast cervical motor root stimulation resulted in responses of normal latency and duration. The phasic stretch reflex had a low threshold, short latency and prolonged duration. It is concluded that in Rett syndrome the corticospinal pathway is intact. The results suggest disordered synaptic control of the Betz cell of the motor cortex and/or the spinal alpha motor neuron, although the involvement of the latter might be a consequence of dysfunction in supraspinal descending motor pathways.
本研究的目的是调查不同年龄的雷特综合征患者皮质脊髓神经元的兴奋性及其通过皮质脊髓束向α运动神经元投射的完整性。采用对运动皮层和颈运动神经根进行电磁刺激的方法,诱发肱二头肌和小鱼际肌的运动动作电位。同时记录肱二头肌的相位牵张反射,以研究脊髓α运动神经元的兴奋性。运动皮层刺激在低阈值时诱发运动动作电位,且潜伏期异常短、持续时间延长。相比之下,颈运动神经根刺激产生的反应潜伏期和持续时间正常。相位牵张反射阈值低、潜伏期短、持续时间延长。得出的结论是,在雷特综合征中皮质脊髓通路是完整的。结果提示,运动皮层的贝茨细胞和/或脊髓α运动神经元的突触控制紊乱,尽管后者受累可能是脊髓上运动下行通路功能障碍的结果。