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Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions
During voluntary contractions, corticomuscular coherence (CMC) is thought to reflect a mutual interaction between cortical and muscle oscillatory activities, respectively measured by electroencephalography (EEG) and electromyography (EMG). However, it remains unclear whether CMC modulation would dep...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973785/ https://www.ncbi.nlm.nih.gov/pubmed/33737659 http://dx.doi.org/10.1038/s41598-021-85851-w |
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author | Glories, Dorian Soulhol, Mathias Amarantini, David Duclay, Julien |
author_facet | Glories, Dorian Soulhol, Mathias Amarantini, David Duclay, Julien |
author_sort | Glories, Dorian |
collection | PubMed |
description | During voluntary contractions, corticomuscular coherence (CMC) is thought to reflect a mutual interaction between cortical and muscle oscillatory activities, respectively measured by electroencephalography (EEG) and electromyography (EMG). However, it remains unclear whether CMC modulation would depend on the contribution of neural mechanisms acting at the spinal level. To this purpose, modulations of CMC were compared during submaximal isometric, shortening and lengthening contractions of the soleus (SOL) and the medial gastrocnemius (MG) with a concurrent analysis of changes in spinal excitability that may be reduced during lengthening contractions. Submaximal contractions intensity was set at 50% of the maximal SOL EMG activity. CMC was computed in the time–frequency domain between the Cz EEG electrode signal and the unrectified SOL or MG EMG signal. Spinal excitability was quantified through normalized Hoffmann (H) reflex amplitude. The results indicate that beta-band CMC and normalized H-reflex were significantly lower in SOL during lengthening compared with isometric contractions, but were similar in MG for all three muscle contraction types. Collectively, these results highlight an effect of contraction type on beta-band CMC, although it may differ between agonist synergist muscles. These novel findings also provide new evidence that beta-band CMC modulation may involve spinal regulatory mechanisms. |
format | Online Article Text |
id | pubmed-7973785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79737852021-03-19 Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions Glories, Dorian Soulhol, Mathias Amarantini, David Duclay, Julien Sci Rep Article During voluntary contractions, corticomuscular coherence (CMC) is thought to reflect a mutual interaction between cortical and muscle oscillatory activities, respectively measured by electroencephalography (EEG) and electromyography (EMG). However, it remains unclear whether CMC modulation would depend on the contribution of neural mechanisms acting at the spinal level. To this purpose, modulations of CMC were compared during submaximal isometric, shortening and lengthening contractions of the soleus (SOL) and the medial gastrocnemius (MG) with a concurrent analysis of changes in spinal excitability that may be reduced during lengthening contractions. Submaximal contractions intensity was set at 50% of the maximal SOL EMG activity. CMC was computed in the time–frequency domain between the Cz EEG electrode signal and the unrectified SOL or MG EMG signal. Spinal excitability was quantified through normalized Hoffmann (H) reflex amplitude. The results indicate that beta-band CMC and normalized H-reflex were significantly lower in SOL during lengthening compared with isometric contractions, but were similar in MG for all three muscle contraction types. Collectively, these results highlight an effect of contraction type on beta-band CMC, although it may differ between agonist synergist muscles. These novel findings also provide new evidence that beta-band CMC modulation may involve spinal regulatory mechanisms. Nature Publishing Group UK 2021-03-18 /pmc/articles/PMC7973785/ /pubmed/33737659 http://dx.doi.org/10.1038/s41598-021-85851-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Glories, Dorian Soulhol, Mathias Amarantini, David Duclay, Julien Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title | Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title_full | Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title_fullStr | Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title_full_unstemmed | Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title_short | Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
title_sort | specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973785/ https://www.ncbi.nlm.nih.gov/pubmed/33737659 http://dx.doi.org/10.1038/s41598-021-85851-w |
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