Motor sequence learning elicits mu peak-specific corticospinal plasticity.

IF 2.1 3区 医学 Q3 NEUROSCIENCES
Tharan Suresh, Fumiaki Iwane, Minsu Zhang, Margaret McElmurry, Muskan Manesiya, Michael V Freedberg, Sara J Hussain
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引用次数: 0

Abstract

Motor cortical (M1) transcranial magnetic stimulation (TMS) interventions increase corticospinal output and improve motor learning when delivered during sensorimotor mu rhythm trough but not peak phases, suggesting that the mechanisms supporting motor learning may be most active during mu trough phases. Based on these findings, we predicted that motor sequence learning-related corticospinal plasticity would be most evident when measured during mu trough phases. Healthy adults were assigned to either a sequence or no-sequence group. Participants in the sequence group practiced the implicit serial reaction time task (SRTT), which contained an embedded, repeating 12-item sequence. Participants in the no-sequence group practiced a version of the SRTT that contained no sequence. We measured mu phase-independent and mu phase-dependent MEP amplitudes using EEG-informed single-pulse TMS before, immediately after, and 30 minutes after the SRTT in both groups. All participants performed a retention test one hour after SRTT acquisition. In both groups, mu phase-independent MEP amplitudes increased following SRTT acquisition, but the pattern of mu phase-dependent MEP amplitude changes after SRTT acquisition differed between groups. Relative to the no-sequence group, the sequence group showed greater peak-specific MEP amplitude increases 30 minutes after SRTT acquisition. Further, the magnitude of these peak-specific MEP amplitude increases was negatively associated with the magnitude of sequence learning. Contrary to our original hypothesis, results revealed that motor sequence learning elicits peak-specific corticospinal plasticity. Findings provide first direct evidence that motor sequence learning recruits mu phase-dependent neurophysiological processes in the human brain.

运动序列学习诱发了脑峰特异性皮质脊髓可塑性。
运动皮质(M1)经颅磁刺激(TMS)干预在感觉运动mu节律期而非峰值期增加皮质脊髓输出并改善运动学习,这表明支持运动学习的机制可能在mu节律期最活跃。基于这些发现,我们预测运动序列学习相关的皮质脊髓可塑性在mu低谷期测量时最为明显。健康成年人被分为顺序组和非顺序组。序列组的参与者练习内隐序列反应时间任务(SRTT),其中包含一个嵌入的,重复的12个项目序列。无序列组的参与者练习了一个没有序列的SRTT版本。在SRTT之前、之后和30分钟后,我们使用脑电图信息的单脉冲TMS测量了两组的mu相位无关和mu相位相关的MEP振幅。所有被试在获得SRTT后1小时进行记忆保留测试。在两组中,获取SRTT后,与mu相无关的MEP振幅均增加,但获取SRTT后,与mu相相关的MEP振幅变化模式存在差异。与无序列组相比,序列组在获得SRTT后30分钟的峰值特异性MEP振幅增加更大。此外,这些峰值特异性MEP幅度的增加幅度与序列学习的幅度呈负相关。与我们最初的假设相反,结果显示运动序列学习引发了峰值特异性皮质脊髓可塑性。研究结果提供了第一个直接证据,证明运动序列学习在人脑中招募了相依赖的神经生理过程。
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来源期刊
Journal of neurophysiology
Journal of neurophysiology 医学-神经科学
CiteScore
4.80
自引率
8.00%
发文量
255
审稿时长
2-3 weeks
期刊介绍: The Journal of Neurophysiology publishes original articles on the function of the nervous system. All levels of function are included, from the membrane and cell to systems and behavior. Experimental approaches include molecular neurobiology, cell culture and slice preparations, membrane physiology, developmental neurobiology, functional neuroanatomy, neurochemistry, neuropharmacology, systems electrophysiology, imaging and mapping techniques, and behavioral analysis. Experimental preparations may be invertebrate or vertebrate species, including humans. Theoretical studies are acceptable if they are tied closely to the interpretation of experimental data and elucidate principles of broad interest.
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