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Geometric models to explore mechanisms of dynamic shape change in skeletal muscle

Skeletal muscle bulges when it contracts. These three-dimensional (3D) dynamic shape changes play an important role in muscle performance by altering the range of fascicle velocities over which a muscle operates. However traditional muscle models are one-dimensional (1D) and cannot fully explain in...

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Autores principales: Dick, Taylor J. M., Wakeling, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990834/
https://www.ncbi.nlm.nih.gov/pubmed/29892420
http://dx.doi.org/10.1098/rsos.172371
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author Dick, Taylor J. M.
Wakeling, James M.
author_facet Dick, Taylor J. M.
Wakeling, James M.
author_sort Dick, Taylor J. M.
collection PubMed
description Skeletal muscle bulges when it contracts. These three-dimensional (3D) dynamic shape changes play an important role in muscle performance by altering the range of fascicle velocities over which a muscle operates. However traditional muscle models are one-dimensional (1D) and cannot fully explain in vivo shape changes. In this study we compared medial gastrocnemius behaviour during human cycling (fascicle length changes and rotations) predicted by a traditional 1D Hill-type model and by models that incorporate two-dimensional (2D) and 3D geometric constraints to in vivo measurements from B-mode ultrasound during a range of mechanical conditions ranging from 14 to 44 N m and 80 to 140 r.p.m. We found that a 1D model predicted fascicle lengths and pennation angles similar to a 2D model that allowed the aponeurosis to stretch, and to a 3D model that allowed for aponeurosis stretch and variable shape changes to occur. This suggests that if the intent of a model is to predict fascicle behaviour alone, then the traditional 1D Hill-type model may be sufficient. Yet, we also caution that 1D models are limited in their ability to infer the mechanisms by which shape changes influence muscle mechanics. To elucidate the mechanisms governing muscle shape change, future efforts should aim to develop imaging techniques able to characterize whole muscle 3D geometry in vivo during active contractions.
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spelling pubmed-59908342018-06-11 Geometric models to explore mechanisms of dynamic shape change in skeletal muscle Dick, Taylor J. M. Wakeling, James M. R Soc Open Sci Biology (Whole Organism) Skeletal muscle bulges when it contracts. These three-dimensional (3D) dynamic shape changes play an important role in muscle performance by altering the range of fascicle velocities over which a muscle operates. However traditional muscle models are one-dimensional (1D) and cannot fully explain in vivo shape changes. In this study we compared medial gastrocnemius behaviour during human cycling (fascicle length changes and rotations) predicted by a traditional 1D Hill-type model and by models that incorporate two-dimensional (2D) and 3D geometric constraints to in vivo measurements from B-mode ultrasound during a range of mechanical conditions ranging from 14 to 44 N m and 80 to 140 r.p.m. We found that a 1D model predicted fascicle lengths and pennation angles similar to a 2D model that allowed the aponeurosis to stretch, and to a 3D model that allowed for aponeurosis stretch and variable shape changes to occur. This suggests that if the intent of a model is to predict fascicle behaviour alone, then the traditional 1D Hill-type model may be sufficient. Yet, we also caution that 1D models are limited in their ability to infer the mechanisms by which shape changes influence muscle mechanics. To elucidate the mechanisms governing muscle shape change, future efforts should aim to develop imaging techniques able to characterize whole muscle 3D geometry in vivo during active contractions. The Royal Society Publishing 2018-05-16 /pmc/articles/PMC5990834/ /pubmed/29892420 http://dx.doi.org/10.1098/rsos.172371 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Dick, Taylor J. M.
Wakeling, James M.
Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title_full Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title_fullStr Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title_full_unstemmed Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title_short Geometric models to explore mechanisms of dynamic shape change in skeletal muscle
title_sort geometric models to explore mechanisms of dynamic shape change in skeletal muscle
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990834/
https://www.ncbi.nlm.nih.gov/pubmed/29892420
http://dx.doi.org/10.1098/rsos.172371
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