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Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity
β Oscillations (13–30 Hz) are ubiquitous in the human motor nervous system. Yet, their origins and roles are unknown. Traditionally, β activity has been treated as a stationary signal. However, recent studies observed that cortical β occurs in “bursting events,” which are transmitted to muscles. Thi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053843/ https://www.ncbi.nlm.nih.gov/pubmed/35351832 http://dx.doi.org/10.1523/JNEUROSCI.1885-21.2022 |
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author | Bräcklein, Mario Barsakcioglu, Deren Y. Del Vecchio, Alessandro Ibáñez, Jaime Farina, Dario |
author_facet | Bräcklein, Mario Barsakcioglu, Deren Y. Del Vecchio, Alessandro Ibáñez, Jaime Farina, Dario |
author_sort | Bräcklein, Mario |
collection | PubMed |
description | β Oscillations (13–30 Hz) are ubiquitous in the human motor nervous system. Yet, their origins and roles are unknown. Traditionally, β activity has been treated as a stationary signal. However, recent studies observed that cortical β occurs in “bursting events,” which are transmitted to muscles. This short-lived nature of β events makes it possible to study the main mechanism of β activity found in the muscles in relation to cortical β. Here, we assessed whether muscle β activity mainly results from cortical projections. We ran two experiments in healthy humans of both sexes (N = 15 and N = 13, respectively) to characterize β activity at the cortical and motor unit (MU) levels during isometric contractions of the tibialis anterior muscle. We found that β rhythms observed at the cortical and MU levels are indeed in bursts. These bursts appeared to be time-locked and had comparable average durations (40–80 ms) and rates (approximately three to four bursts per second). To further confirm that cortical and MU β have the same source, we used a novel operant conditioning framework to allow subjects to volitionally modulate MU β. We showed that volitional modulation of β activity at the MU level was possible with minimal subject learning and was paralleled by similar changes in cortical β activity. These results support the hypothesis that MU β mainly results from cortical projections. Moreover, they demonstrate the possibility to decode cortical β activity from MU recordings, with a potential translation to future neural interfaces that use peripheral information to identify and modulate activity in the central nervous system. SIGNIFICANCE STATEMENT We show for the first time that β activity in motor unit (MU) populations occurs in bursting events. These bursts observed in the output of the spinal cord appear to be time-locked and share similar characteristics of β activity at the cortical level, such as the duration and rate at which they occur. Moreover, when subjects were exposed to a novel operant conditioning paradigm and modulated MU β activity, cortical β activity changed in a similar way as peripheral β. These results provide evidence for a strong correspondence between cortical and peripheral β activity, demonstrating the cortical origin of peripheral β and opening the pathway for a new generation of neural interfaces. |
format | Online Article Text |
id | pubmed-9053843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-90538432022-05-02 Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity Bräcklein, Mario Barsakcioglu, Deren Y. Del Vecchio, Alessandro Ibáñez, Jaime Farina, Dario J Neurosci Research Articles β Oscillations (13–30 Hz) are ubiquitous in the human motor nervous system. Yet, their origins and roles are unknown. Traditionally, β activity has been treated as a stationary signal. However, recent studies observed that cortical β occurs in “bursting events,” which are transmitted to muscles. This short-lived nature of β events makes it possible to study the main mechanism of β activity found in the muscles in relation to cortical β. Here, we assessed whether muscle β activity mainly results from cortical projections. We ran two experiments in healthy humans of both sexes (N = 15 and N = 13, respectively) to characterize β activity at the cortical and motor unit (MU) levels during isometric contractions of the tibialis anterior muscle. We found that β rhythms observed at the cortical and MU levels are indeed in bursts. These bursts appeared to be time-locked and had comparable average durations (40–80 ms) and rates (approximately three to four bursts per second). To further confirm that cortical and MU β have the same source, we used a novel operant conditioning framework to allow subjects to volitionally modulate MU β. We showed that volitional modulation of β activity at the MU level was possible with minimal subject learning and was paralleled by similar changes in cortical β activity. These results support the hypothesis that MU β mainly results from cortical projections. Moreover, they demonstrate the possibility to decode cortical β activity from MU recordings, with a potential translation to future neural interfaces that use peripheral information to identify and modulate activity in the central nervous system. SIGNIFICANCE STATEMENT We show for the first time that β activity in motor unit (MU) populations occurs in bursting events. These bursts observed in the output of the spinal cord appear to be time-locked and share similar characteristics of β activity at the cortical level, such as the duration and rate at which they occur. Moreover, when subjects were exposed to a novel operant conditioning paradigm and modulated MU β activity, cortical β activity changed in a similar way as peripheral β. These results provide evidence for a strong correspondence between cortical and peripheral β activity, demonstrating the cortical origin of peripheral β and opening the pathway for a new generation of neural interfaces. Society for Neuroscience 2022-04-27 /pmc/articles/PMC9053843/ /pubmed/35351832 http://dx.doi.org/10.1523/JNEUROSCI.1885-21.2022 Text en Copyright © 2022 Bräcklein et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Articles Bräcklein, Mario Barsakcioglu, Deren Y. Del Vecchio, Alessandro Ibáñez, Jaime Farina, Dario Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title | Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title_full | Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title_fullStr | Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title_full_unstemmed | Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title_short | Reading and Modulating Cortical β Bursts from Motor Unit Spiking Activity |
title_sort | reading and modulating cortical β bursts from motor unit spiking activity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053843/ https://www.ncbi.nlm.nih.gov/pubmed/35351832 http://dx.doi.org/10.1523/JNEUROSCI.1885-21.2022 |
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