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Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons

Unpowered exoskeletons with springs in parallel to human plantar flexor muscle-tendons can reduce the metabolic cost of walking. We used ultrasound imaging to look ‘under the skin’ and measure how exoskeleton stiffness alters soleus muscle contractile dynamics and shapes the user’s metabolic rate du...

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Autores principales: Nuckols, R. W., Dick, T. J. M., Beck, O. N., Sawicki, G. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046782/
https://www.ncbi.nlm.nih.gov/pubmed/32109239
http://dx.doi.org/10.1038/s41598-020-60360-4
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author Nuckols, R. W.
Dick, T. J. M.
Beck, O. N.
Sawicki, G. S.
author_facet Nuckols, R. W.
Dick, T. J. M.
Beck, O. N.
Sawicki, G. S.
author_sort Nuckols, R. W.
collection PubMed
description Unpowered exoskeletons with springs in parallel to human plantar flexor muscle-tendons can reduce the metabolic cost of walking. We used ultrasound imaging to look ‘under the skin’ and measure how exoskeleton stiffness alters soleus muscle contractile dynamics and shapes the user’s metabolic rate during walking. Eleven participants (4F, 7M; age: 27.7 ± 3.3 years) walked on a treadmill at 1.25 m s(−1) and 0% grade with elastic ankle exoskeletons (rotational stiffness: 0–250 Nm rad(−1)) in one training and two testing days. Metabolic savings were maximized (4.2%) at a stiffness of 50 Nm rad(−1). As exoskeleton stiffness increased, the soleus muscle operated at longer lengths and improved economy (force/activation) during early stance, but this benefit was offset by faster shortening velocity and poorer economy in late stance. Changes in soleus activation rate correlated with changes in users’ metabolic rate (p = 0.038, R(2) = 0.44), highlighting a crucial link between muscle neuromechanics and exoskeleton performance; perhaps informing future ‘muscle-in-the loop’ exoskeleton controllers designed to steer contractile dynamics toward more economical force production.
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spelling pubmed-70467822020-03-05 Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons Nuckols, R. W. Dick, T. J. M. Beck, O. N. Sawicki, G. S. Sci Rep Article Unpowered exoskeletons with springs in parallel to human plantar flexor muscle-tendons can reduce the metabolic cost of walking. We used ultrasound imaging to look ‘under the skin’ and measure how exoskeleton stiffness alters soleus muscle contractile dynamics and shapes the user’s metabolic rate during walking. Eleven participants (4F, 7M; age: 27.7 ± 3.3 years) walked on a treadmill at 1.25 m s(−1) and 0% grade with elastic ankle exoskeletons (rotational stiffness: 0–250 Nm rad(−1)) in one training and two testing days. Metabolic savings were maximized (4.2%) at a stiffness of 50 Nm rad(−1). As exoskeleton stiffness increased, the soleus muscle operated at longer lengths and improved economy (force/activation) during early stance, but this benefit was offset by faster shortening velocity and poorer economy in late stance. Changes in soleus activation rate correlated with changes in users’ metabolic rate (p = 0.038, R(2) = 0.44), highlighting a crucial link between muscle neuromechanics and exoskeleton performance; perhaps informing future ‘muscle-in-the loop’ exoskeleton controllers designed to steer contractile dynamics toward more economical force production. Nature Publishing Group UK 2020-02-27 /pmc/articles/PMC7046782/ /pubmed/32109239 http://dx.doi.org/10.1038/s41598-020-60360-4 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nuckols, R. W.
Dick, T. J. M.
Beck, O. N.
Sawicki, G. S.
Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title_full Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title_fullStr Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title_full_unstemmed Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title_short Ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
title_sort ultrasound imaging links soleus muscle neuromechanics and energetics during human walking with elastic ankle exoskeletons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046782/
https://www.ncbi.nlm.nih.gov/pubmed/32109239
http://dx.doi.org/10.1038/s41598-020-60360-4
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