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Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion

Coupling between cortical oscillations and muscle activity facilitates neuronal communication during motor control. The linear part of this coupling, known as corticomuscular coherence, has received substantial attention, even though neuronal communication underlying motor control has been demonstra...

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Autores principales: Yang, Yuan, Solis-Escalante, Teodoro, van de Ruit, Mark, van der Helm, Frans C. T., Schouten, Alfred C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138209/
https://www.ncbi.nlm.nih.gov/pubmed/27999537
http://dx.doi.org/10.3389/fncom.2016.00126
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author Yang, Yuan
Solis-Escalante, Teodoro
van de Ruit, Mark
van der Helm, Frans C. T.
Schouten, Alfred C.
author_facet Yang, Yuan
Solis-Escalante, Teodoro
van de Ruit, Mark
van der Helm, Frans C. T.
Schouten, Alfred C.
author_sort Yang, Yuan
collection PubMed
description Coupling between cortical oscillations and muscle activity facilitates neuronal communication during motor control. The linear part of this coupling, known as corticomuscular coherence, has received substantial attention, even though neuronal communication underlying motor control has been demonstrated to be highly nonlinear. A full assessment of corticomuscular coupling, including the nonlinear part, is essential to understand the neuronal communication within the sensorimotor system. In this study, we applied the recently developed n:m coherence method to assess nonlinear corticomuscular coupling during isotonic wrist flexion. The n:m coherence is a generalized metric for quantifying nonlinear cross-frequency coupling as well as linear iso-frequency coupling. By using independent component analysis (ICA) and equivalent current dipole source localization, we identify four sensorimotor related brain areas based on the locations of the dipoles, i.e., the contralateral primary sensorimotor areas, supplementary motor area (SMA), prefrontal area (PFA) and posterior parietal cortex (PPC). For all these areas, linear coupling between electroencephalogram (EEG) and electromyogram (EMG) is present with peaks in the beta band (15–35 Hz), while nonlinear coupling is detected with both integer (1:2, 1:3, 1:4) and non-integer (2:3) harmonics. Significant differences between brain areas is shown in linear coupling with stronger coherence for the primary sensorimotor areas and motor association cortices (SMA, PFA) compared to the sensory association area (PPC); but not for the nonlinear coupling. Moreover, the detected nonlinear coupling is similar to previously reported nonlinear coupling of cortical activity to somatosensory stimuli. We suggest that the descending motor pathways mainly contribute to linear corticomuscular coupling, while nonlinear coupling likely originates from sensory feedback.
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spelling pubmed-51382092016-12-20 Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion Yang, Yuan Solis-Escalante, Teodoro van de Ruit, Mark van der Helm, Frans C. T. Schouten, Alfred C. Front Comput Neurosci Neuroscience Coupling between cortical oscillations and muscle activity facilitates neuronal communication during motor control. The linear part of this coupling, known as corticomuscular coherence, has received substantial attention, even though neuronal communication underlying motor control has been demonstrated to be highly nonlinear. A full assessment of corticomuscular coupling, including the nonlinear part, is essential to understand the neuronal communication within the sensorimotor system. In this study, we applied the recently developed n:m coherence method to assess nonlinear corticomuscular coupling during isotonic wrist flexion. The n:m coherence is a generalized metric for quantifying nonlinear cross-frequency coupling as well as linear iso-frequency coupling. By using independent component analysis (ICA) and equivalent current dipole source localization, we identify four sensorimotor related brain areas based on the locations of the dipoles, i.e., the contralateral primary sensorimotor areas, supplementary motor area (SMA), prefrontal area (PFA) and posterior parietal cortex (PPC). For all these areas, linear coupling between electroencephalogram (EEG) and electromyogram (EMG) is present with peaks in the beta band (15–35 Hz), while nonlinear coupling is detected with both integer (1:2, 1:3, 1:4) and non-integer (2:3) harmonics. Significant differences between brain areas is shown in linear coupling with stronger coherence for the primary sensorimotor areas and motor association cortices (SMA, PFA) compared to the sensory association area (PPC); but not for the nonlinear coupling. Moreover, the detected nonlinear coupling is similar to previously reported nonlinear coupling of cortical activity to somatosensory stimuli. We suggest that the descending motor pathways mainly contribute to linear corticomuscular coupling, while nonlinear coupling likely originates from sensory feedback. Frontiers Media S.A. 2016-12-06 /pmc/articles/PMC5138209/ /pubmed/27999537 http://dx.doi.org/10.3389/fncom.2016.00126 Text en Copyright © 2016 Yang, Solis-Escalante, van de Ruit, van der Helm and Schouten. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Yang, Yuan
Solis-Escalante, Teodoro
van de Ruit, Mark
van der Helm, Frans C. T.
Schouten, Alfred C.
Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title_full Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title_fullStr Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title_full_unstemmed Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title_short Nonlinear Coupling between Cortical Oscillations and Muscle Activity during Isotonic Wrist Flexion
title_sort nonlinear coupling between cortical oscillations and muscle activity during isotonic wrist flexion
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138209/
https://www.ncbi.nlm.nih.gov/pubmed/27999537
http://dx.doi.org/10.3389/fncom.2016.00126
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