Department of Neurology, Division of Neuroscience, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
J Physiol. 2009 Oct 15;587(Pt 20):4845-62. doi: 10.1113/jphysiol.2009.179101. Epub 2009 Sep 1.
Motor cortical plasticity induced by repetitive transcranial magnetic stimulation (rTMS) sometimes depends on the prior history of neuronal activity. These effects of preceding stimulation on subsequent rTMS-induced plasticity have been suggested to share a similar mechanism to that of metaplasticity, a homeostatic regulation of synaptic plasticity. To explore metaplasticity in humans, many investigations have used designs in which both priming and conditioning are applied over the primary motor cortex (M1), but the effects of priming stimulation over other motor-related cortical areas have not been well documented. Since the supplementary motor area (SMA) has anatomical and functional cortico-cortical connections with M1, here we studied the homeostatic effects of priming stimulation over the SMA on subsequent rTMS-induced plasticity of M1. For priming and subsequent conditioning, we employed a new rTMS protocol, quadripulse stimulation (QPS), which produces a broad range of motor cortical plasticity depending on the interval of the pulses within a burst. The plastic changes induced by QPS at various intervals were altered by priming stimulation over the SMA, which did not change motor-evoked potential sizes on its own but specifically modulated the excitatory I-wave circuits. The data support the view that the homeostatic changes are mediated via mechanisms of metaplasticity and highlight an important interplay between M1 and SMA regarding homeostatic plasticity in humans.
经重复经颅磁刺激(rTMS)诱导的运动皮质可塑性有时取决于神经元活动的先前历史。先前刺激对随后 rTMS 诱导的可塑性的这些影响被认为与易化作用具有相似的机制,即突触可塑性的同型调节。为了在人类中探索易化作用,许多研究采用了在初级运动皮质(M1)上同时施加启动和调节的设计,但启动刺激对其他与运动相关的皮质区域的影响尚未得到很好的记录。由于补充运动区(SMA)与 M1 具有解剖学和功能上的皮质-皮质连接,因此我们在这里研究了 SMA 上的启动刺激对随后 M1 的 rTMS 诱导可塑性的同型调节作用。对于启动和随后的调节,我们采用了一种新的 rTMS 方案,即四脉冲刺激(QPS),根据脉冲在爆发中的间隔,它会产生广泛的运动皮质可塑性。QPS 在不同间隔引起的可塑性变化被 SMA 上的启动刺激所改变,启动刺激本身不会改变运动诱发电位的大小,但专门调节了兴奋性 I 波电路。这些数据支持了同型调节变化是通过易化作用的机制介导的观点,并突出了 M1 和 SMA 之间关于人类同型调节可塑性的重要相互作用。