Primary motor cortical metaplasticity induced by priming over the supplementary motor area

被引:72
作者
Hamada, Masashi [1 ]
Hanajima, Ritsuko
Terao, Yasuo
Okabe, Shingo
Nakatani-Enomoto, Setsu [2 ]
Furubayashi, Toshiaki [2 ]
Matsumoto, Hideyuki
Shirota, Yuichiro
Ohminami, Shinya
Ugawa, Yoshikazu [2 ]
机构
[1] Univ Tokyo, Dept Neurol, Div Neurosci, Grad Sch Med,Bunkyo Ku, Tokyo 1138655, Japan
[2] Fukushima Med Univ, Sch Med, Dept Neurol, Fukushima, Japan
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2009年 / 587卷 / 20期
关键词
TRANSCRANIAL MAGNETIC STIMULATION; THETA-BURST-STIMULATION; LONG-TERM POTENTIATION; PAIRED ASSOCIATIVE STIMULATION; FREQUENCY SYNAPTIC ACTIVITY; MACAQUE MONKEY; VISUAL-CORTEX; CORTICOSPINAL EXCITABILITY; HOMEOSTATIC PLASTICITY; SEQUENTIAL-PROCEDURES;
D O I
10.1113/jphysiol.2009.179101
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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 M I and SMA regarding homeostatic plasticity in humans.
引用
收藏
页码:4845 / 4862
页数:18
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