Cargando…
Spatiotemporal organisation of human sensorimotor beta burst activity
Beta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, bu...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110262/ https://www.ncbi.nlm.nih.gov/pubmed/36961500 http://dx.doi.org/10.7554/eLife.80160 |
_version_ | 1785027233300086784 |
---|---|
author | Zich, Catharina Quinn, Andrew J Bonaiuto, James J O'Neill, George Mardell, Lydia C Ward, Nick S Bestmann, Sven |
author_facet | Zich, Catharina Quinn, Andrew J Bonaiuto, James J O'Neill, George Mardell, Lydia C Ward, Nick S Bestmann, Sven |
author_sort | Zich, Catharina |
collection | PubMed |
description | Beta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, but their precise spatial, spectral, and temporal structure remains unclear. Specifically, a role for beta burst activity in information coding and communication suggests spatiotemporal patterns, or travelling wave activity, along specific anatomical gradients. We here show in human magnetoencephalography recordings that burst activity in sensorimotor cortex occurs in planar spatiotemporal wave-like patterns that dominate along two axes either parallel or perpendicular to the central sulcus. Moreover, we find that the two propagation directions are characterised by distinct anatomical and physiological features. Finally, our results suggest that sensorimotor beta bursts occurring before and after a movement can be distinguished by their anatomical, spectral, and spatiotemporal characteristics, indicating distinct functional roles. |
format | Online Article Text |
id | pubmed-10110262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-101102622023-04-18 Spatiotemporal organisation of human sensorimotor beta burst activity Zich, Catharina Quinn, Andrew J Bonaiuto, James J O'Neill, George Mardell, Lydia C Ward, Nick S Bestmann, Sven eLife Neuroscience Beta oscillations in human sensorimotor cortex are hallmark signatures of healthy and pathological movement. In single trials, beta oscillations include bursts of intermittent, transient periods of high-power activity. These burst events have been linked to a range of sensory and motor processes, but their precise spatial, spectral, and temporal structure remains unclear. Specifically, a role for beta burst activity in information coding and communication suggests spatiotemporal patterns, or travelling wave activity, along specific anatomical gradients. We here show in human magnetoencephalography recordings that burst activity in sensorimotor cortex occurs in planar spatiotemporal wave-like patterns that dominate along two axes either parallel or perpendicular to the central sulcus. Moreover, we find that the two propagation directions are characterised by distinct anatomical and physiological features. Finally, our results suggest that sensorimotor beta bursts occurring before and after a movement can be distinguished by their anatomical, spectral, and spatiotemporal characteristics, indicating distinct functional roles. eLife Sciences Publications, Ltd 2023-03-24 /pmc/articles/PMC10110262/ /pubmed/36961500 http://dx.doi.org/10.7554/eLife.80160 Text en © 2023, Zich et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Zich, Catharina Quinn, Andrew J Bonaiuto, James J O'Neill, George Mardell, Lydia C Ward, Nick S Bestmann, Sven Spatiotemporal organisation of human sensorimotor beta burst activity |
title | Spatiotemporal organisation of human sensorimotor beta burst activity |
title_full | Spatiotemporal organisation of human sensorimotor beta burst activity |
title_fullStr | Spatiotemporal organisation of human sensorimotor beta burst activity |
title_full_unstemmed | Spatiotemporal organisation of human sensorimotor beta burst activity |
title_short | Spatiotemporal organisation of human sensorimotor beta burst activity |
title_sort | spatiotemporal organisation of human sensorimotor beta burst activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110262/ https://www.ncbi.nlm.nih.gov/pubmed/36961500 http://dx.doi.org/10.7554/eLife.80160 |
work_keys_str_mv | AT zichcatharina spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT quinnandrewj spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT bonaiutojamesj spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT oneillgeorge spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT mardelllydiac spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT wardnicks spatiotemporalorganisationofhumansensorimotorbetaburstactivity AT bestmannsven spatiotemporalorganisationofhumansensorimotorbetaburstactivity |