Khedr Eman M, Gilio Francesca, Rothwell John
Department of Neurology, The University Hospital, Assiut, Egypt.
Clin Neurophysiol. 2004 Jun;115(6):1259-63. doi: 10.1016/j.clinph.2003.08.025.
Following a previous report [Bestmann et al. Clin Neurophysiol 2004;115:755-64] that pairs of subthreshold pulses of transcranial magnetic stimulation (TMS) can show temporal summation, we explored whether repeated application of pairs of stimulation could produce long-lasting after effects on the excitability of the human motor cortex.
Twelve healthy subjects received 25 min repetitive paired pulse magnetic stimulation (paired rTMS) given at a frequency of about 0.6 Hz over the left primary motor cortex (500 paired stimuli in total). The interval between the paired stimuli was 3 ms and the intensity of both stimuli was 80% of active motor threshold. The resting and active motor threshold, MEP recruitment curve, short interval intracortical inhibition (SICI) and facilitation, and the duration of the cortical silent period (SP) were tested for the right first interosseous muscle (FDI) before and two times after the end of 25 min paired rTMS.
Prolonged subthreshold paired rTMS produced a significant decrease in excitability in the corticospinal projection to FDI: resting motor threshold was significantly increased and MEP recruitment was significantly decreased, SICI was significantly increased at 2 and 4 ms and the SP was significantly increased in duration.
Prolonged low frequency paired rTMS at subthreshold intensity can modulate cortical excitability by producing inhibitory effects that outlast the period of stimulation.
继之前一份报告[贝斯特曼等人。《临床神经生理学》2004年;115:755 - 64]指出经颅磁刺激(TMS)的亚阈值脉冲对可表现出时间总和效应后,我们探究了重复施加刺激对是否会对人类运动皮层的兴奋性产生持久的后效应。
12名健康受试者在左侧初级运动皮层接受了25分钟的重复配对脉冲磁刺激(配对rTMS),刺激频率约为0.6赫兹(总共500对刺激)。配对刺激之间的间隔为3毫秒,且两个刺激的强度均为运动激活阈值的80%。在25分钟配对rTMS结束前及结束后两次,对右侧第一骨间肌(FDI)的静息和运动激活阈值、运动诱发电位(MEP)募集曲线、短间隔皮质内抑制(SICI)和易化以及皮质静息期(SP)的持续时间进行了测试。
长时间的亚阈值配对rTMS使皮质脊髓投射到FDI的兴奋性显著降低:静息运动阈值显著升高,MEP募集显著减少,在2毫秒和4毫秒时SICI显著增加,且SP持续时间显著延长。
长时间的低频亚阈值强度配对rTMS可通过产生持续超过刺激期的抑制性效应来调节皮质兴奋性。