运动兴奋性的调节反映了神经振荡的行波。

IF 6.9 1区 生物学 Q1 CELL BIOLOGY
Cell reports Pub Date : 2025-06-24 Epub Date: 2025-06-14 DOI:10.1016/j.celrep.2025.115864
Zachary J Haigh, Harry Tran, Taylor Berger, Sina Shirinpour, Ivan Alekseichuk, Seth Koenig, Jan Zimmermann, Robert McGovern, David Darrow, Alexander Herman, Miles Wischnewski, Alexander Opitz
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引用次数: 0

摘要

神经行波是人脑中一种重要的内源性现象,具有结构和功能上的相关性。这些波通常通过脑电图(EEG)或皮质电图(ECoG)记录,与一系列脑过程有关。然而,目前尚不清楚它们如何影响大脑区域的神经兴奋性。实时控制脑刺激的进步提供了比较行波和兴奋的机会。本研究利用实时脑电图控制的经颅磁刺激(TMS)研究了感觉运动mu (8-13 Hz)和beta (14-30 Hz)行波对运动皮层兴奋性的影响。我们观察了中外侧方向的梯度,然后用人类参与者和非人灵长类动物的ECoG记录验证了这些发现。我们的研究结果表明,神经元的兴奋性反映了感觉运动行波的自然模式。这为行波调节人类神经兴奋性提供了重要证据。这为更有效的刺激方案提供了可能性,这些方案与大脑内在动力学相一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of motor excitability reflects traveling waves of neural oscillations.

Neural traveling waves represent an important endogenous phenomenon with structural and functional relevance in the human brain. These waves, commonly recorded via electroencephalogram (EEG) or electrocorticography (ECoG), are implicated in a range of brain processes. However, it remains unclear how they influence neural excitability across brain regions. Advancements in real-time control of brain stimulation present opportunities to compare traveling waves and excitation. Here, we investigate how sensorimotor mu (8-13 Hz) and beta (14-30 Hz) traveling waves affect motor cortex excitability using real-time EEG-controlled transcranial magnetic stimulation (TMS). We observed gradients in the mediolateral direction and then validated these findings using ECoG recordings in a human participant and a nonhuman primate. Our results demonstrate that neuronal excitability reflects the natural patterns of sensorimotor traveling waves. This provides important evidence of traveling waves modulating neural excitability in humans. This opens possibilities for more effective stimulation protocols aligned with intrinsic brain dynamics.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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