Kurokawa-Kuroda Tomomi, Ogata Katsuya, Suga Rie, Goto Yoshinobu, Taniwaki Takayuki, Kira Jun-Ichi, Tobimatsu Shozo
Department of Clinical Neurophysiology, Neurological Institute, Faculty of Medicine, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Fukuoka, Japan.
Clin Neurophysiol. 2007 Jun;118(6):1198-203. doi: 10.1016/j.clinph.2007.03.006. Epub 2007 Apr 23.
Transcranial magnetic stimulation (TMS) over the leg motor area elicits a soleus primary response (SPR) and a soleus late response (SLR). We evaluated the influence of the cerebellofugal pathway on the SPR and SLR in patients with 'pure' cerebellar ataxia.
SPRs and SLRs were recorded from 11 healthy subjects and 9 patients with 'pure' cerebellar cortical degeneration; 5 with spinocerebellar ataxia type 6 (SCA6), and 4 with late cortical cerebellar ataxia (LCCA). In addition, three patients with localized cerebellar lesions were tested.
The SPR latency was significantly longer in patients than in controls, but primary responses in the tibialis anterior muscle were normal. The frequency of abnormal SLR was 38.9% in the supine position and 83.3% in the standing position. Two out of three patients with localized cerebellar lesions also showed abnormal SLR.
Altered SPRs in patients may result from a dysfunction of the primary motor cortex caused by crossed cerebello-cerebral diaschisis. In addition, our results suggest that 'pure' cerebellar degeneration involves the mechanism responsible for evoking SLR which is related to the control of posture.
SLR can be a useful neurophysiological parameter for evaluating cerebellofugal function.
对腿部运动区进行经颅磁刺激(TMS)可诱发比目鱼肌主反应(SPR)和比目鱼肌迟发反应(SLR)。我们评估了小脑传出通路对“单纯”小脑性共济失调患者SPR和SLR的影响。
记录了11名健康受试者和9名“单纯”小脑皮质变性患者的SPR和SLR;其中5例为6型脊髓小脑共济失调(SCA6),4例为晚期皮质小脑共济失调(LCCA)。此外,还对3例局限性小脑病变患者进行了测试。
患者的SPR潜伏期明显长于对照组,但胫前肌的主反应正常。仰卧位时异常SLR的发生率为38.9%,站立位时为83.3%。3例局限性小脑病变患者中有2例也表现出异常SLR。
患者SPR改变可能是由于交叉性大脑小脑失联络导致初级运动皮层功能障碍所致。此外,我们的结果表明,“单纯”小脑变性涉及诱发与姿势控制相关的SLR的机制。
SLR可作为评估小脑传出功能的有用神经生理学参数。