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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...

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Autores principales: Bräcklein, Mario, Barsakcioglu, Deren Y., Del Vecchio, Alessandro, Ibáñez, Jaime, Farina, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
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.
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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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