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Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans
Brain-computer interfaces provide an artificial link by which the brain can directly interact with the environment. To achieve fine brain-computer interface control, participants must modulate the patterns of the cortical oscillations generated from the motor and somatosensory cortices. However, it...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288463/ https://www.ncbi.nlm.nih.gov/pubmed/35842523 http://dx.doi.org/10.1038/s42003-022-03665-6 |
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author | Kasahara, Kazumi DaSalla, Charles S. Honda, Manabu Hanakawa, Takashi |
author_facet | Kasahara, Kazumi DaSalla, Charles S. Honda, Manabu Hanakawa, Takashi |
author_sort | Kasahara, Kazumi |
collection | PubMed |
description | Brain-computer interfaces provide an artificial link by which the brain can directly interact with the environment. To achieve fine brain-computer interface control, participants must modulate the patterns of the cortical oscillations generated from the motor and somatosensory cortices. However, it remains unclear how humans regulate cortical oscillations, the controllability of which substantially varies across individuals. Here, we performed simultaneous electroencephalography (to assess brain-computer interface control) and functional magnetic resonance imaging (to measure brain activity) in healthy participants. Self-regulation of cortical oscillations induced activity in the basal ganglia-cortical network and the neurofeedback control network. Successful self-regulation correlated with striatal activity in the basal ganglia-cortical network, through which patterns of cortical oscillations were likely modulated. Moreover, basal ganglia-cortical network and neurofeedback control network connectivity correlated with strong and weak self-regulation, respectively. The findings indicate that the basal ganglia-cortical network is important for self-regulation, the understanding of which should help advance brain-computer interface technology. |
format | Online Article Text |
id | pubmed-9288463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92884632022-07-18 Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans Kasahara, Kazumi DaSalla, Charles S. Honda, Manabu Hanakawa, Takashi Commun Biol Article Brain-computer interfaces provide an artificial link by which the brain can directly interact with the environment. To achieve fine brain-computer interface control, participants must modulate the patterns of the cortical oscillations generated from the motor and somatosensory cortices. However, it remains unclear how humans regulate cortical oscillations, the controllability of which substantially varies across individuals. Here, we performed simultaneous electroencephalography (to assess brain-computer interface control) and functional magnetic resonance imaging (to measure brain activity) in healthy participants. Self-regulation of cortical oscillations induced activity in the basal ganglia-cortical network and the neurofeedback control network. Successful self-regulation correlated with striatal activity in the basal ganglia-cortical network, through which patterns of cortical oscillations were likely modulated. Moreover, basal ganglia-cortical network and neurofeedback control network connectivity correlated with strong and weak self-regulation, respectively. The findings indicate that the basal ganglia-cortical network is important for self-regulation, the understanding of which should help advance brain-computer interface technology. Nature Publishing Group UK 2022-07-16 /pmc/articles/PMC9288463/ /pubmed/35842523 http://dx.doi.org/10.1038/s42003-022-03665-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kasahara, Kazumi DaSalla, Charles S. Honda, Manabu Hanakawa, Takashi Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title | Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title_full | Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title_fullStr | Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title_full_unstemmed | Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title_short | Basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
title_sort | basal ganglia-cortical connectivity underlies self-regulation of brain oscillations in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288463/ https://www.ncbi.nlm.nih.gov/pubmed/35842523 http://dx.doi.org/10.1038/s42003-022-03665-6 |
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