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Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study

Previous electro‐ or magnetoencephalography (Electro/Magneto EncephaloGraphic; E/MEG) studies using a correlative approach have shown that β (13–30 Hz) oscillations emerging in the primary motor cortex (M1) are implicated in regulating motor response vigor and associated with an anti‐kinetic role, t...

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Autores principales: Uehara, Kazumasa, Fine, Justin M., Santello, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875933/
https://www.ncbi.nlm.nih.gov/pubmed/36419365
http://dx.doi.org/10.1002/hbm.26149
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author Uehara, Kazumasa
Fine, Justin M.
Santello, Marco
author_facet Uehara, Kazumasa
Fine, Justin M.
Santello, Marco
author_sort Uehara, Kazumasa
collection PubMed
description Previous electro‐ or magnetoencephalography (Electro/Magneto EncephaloGraphic; E/MEG) studies using a correlative approach have shown that β (13–30 Hz) oscillations emerging in the primary motor cortex (M1) are implicated in regulating motor response vigor and associated with an anti‐kinetic role, that is, slowness of movement. However, the functional role of M1 β oscillations in regulation of motor responses remains unclear. To address this gap, we combined EEG with rhythmic TMS (rhTMS) delivered to M1 at the β (20 Hz) frequency shortly before subjects performed an isometric ramp‐and‐hold finger force production task at three force levels. rhTMS is a novel approach that can modulate rhythmic patterns of neural activity. β‐rhTMS over M1 induced a modulation of neural oscillations to β frequency in the sensorimotor area and reduced peak force rate during the ramp‐up period relative to sham and catch trials. Interestingly, this rhTMS effect occurred only in the large force production condition. To distinguish whether the effects of rhTMS on EEG and behavior stemmed from phase‐resetting by each magnetic pulse or neural entrainment by the periodicity of rhTMS, we performed a control experiment using arrhythmic TMS (arTMS). arTMS did not induce changes in EEG oscillations nor peak force rate during the rump‐up period. Our results provide novel evidence that β neural oscillations emerging the sensorimotor area influence the regulation of motor response vigor. Furthermore, our findings further demonstrate that rhTMS is a promising tool for tuning neural oscillations to the target frequency.
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spelling pubmed-98759332023-01-25 Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study Uehara, Kazumasa Fine, Justin M. Santello, Marco Hum Brain Mapp Research Articles Previous electro‐ or magnetoencephalography (Electro/Magneto EncephaloGraphic; E/MEG) studies using a correlative approach have shown that β (13–30 Hz) oscillations emerging in the primary motor cortex (M1) are implicated in regulating motor response vigor and associated with an anti‐kinetic role, that is, slowness of movement. However, the functional role of M1 β oscillations in regulation of motor responses remains unclear. To address this gap, we combined EEG with rhythmic TMS (rhTMS) delivered to M1 at the β (20 Hz) frequency shortly before subjects performed an isometric ramp‐and‐hold finger force production task at three force levels. rhTMS is a novel approach that can modulate rhythmic patterns of neural activity. β‐rhTMS over M1 induced a modulation of neural oscillations to β frequency in the sensorimotor area and reduced peak force rate during the ramp‐up period relative to sham and catch trials. Interestingly, this rhTMS effect occurred only in the large force production condition. To distinguish whether the effects of rhTMS on EEG and behavior stemmed from phase‐resetting by each magnetic pulse or neural entrainment by the periodicity of rhTMS, we performed a control experiment using arrhythmic TMS (arTMS). arTMS did not induce changes in EEG oscillations nor peak force rate during the rump‐up period. Our results provide novel evidence that β neural oscillations emerging the sensorimotor area influence the regulation of motor response vigor. Furthermore, our findings further demonstrate that rhTMS is a promising tool for tuning neural oscillations to the target frequency. John Wiley & Sons, Inc. 2022-11-23 /pmc/articles/PMC9875933/ /pubmed/36419365 http://dx.doi.org/10.1002/hbm.26149 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Uehara, Kazumasa
Fine, Justin M.
Santello, Marco
Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title_full Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title_fullStr Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title_full_unstemmed Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title_short Modulation of cortical beta oscillations influences motor vigor: A rhythmic TMS‐EEG study
title_sort modulation of cortical beta oscillations influences motor vigor: a rhythmic tms‐eeg study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875933/
https://www.ncbi.nlm.nih.gov/pubmed/36419365
http://dx.doi.org/10.1002/hbm.26149
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