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
{"title":"运动兴奋性的调节反映了神经振荡的行波。","authors":"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","doi":"10.1016/j.celrep.2025.115864","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":"44 6","pages":"115864"},"PeriodicalIF":6.9000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12257788/pdf/","citationCount":"0","resultStr":"{\"title\":\"Modulation of motor excitability reflects traveling waves of neural oscillations.\",\"authors\":\"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\",\"doi\":\"10.1016/j.celrep.2025.115864\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":9798,\"journal\":{\"name\":\"Cell reports\",\"volume\":\"44 6\",\"pages\":\"115864\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12257788/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell reports\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.celrep.2025.115864\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.celrep.2025.115864","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
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.
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.