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Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis

Skeletal muscle responds to passive overstretch through sarcomerogenesis, the creation and serial deposition of new sarcomere units. Sarcomerogenesis is critical to muscle function: It gradually re-positions the muscle back into its optimal operating regime. Animal models of immobilization, limb len...

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Autores principales: Zöllner, Alexander M., Abilez, Oscar J., Böl, Markus, Kuhl, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462200/
https://www.ncbi.nlm.nih.gov/pubmed/23049683
http://dx.doi.org/10.1371/journal.pone.0045661
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author Zöllner, Alexander M.
Abilez, Oscar J.
Böl, Markus
Kuhl, Ellen
author_facet Zöllner, Alexander M.
Abilez, Oscar J.
Böl, Markus
Kuhl, Ellen
author_sort Zöllner, Alexander M.
collection PubMed
description Skeletal muscle responds to passive overstretch through sarcomerogenesis, the creation and serial deposition of new sarcomere units. Sarcomerogenesis is critical to muscle function: It gradually re-positions the muscle back into its optimal operating regime. Animal models of immobilization, limb lengthening, and tendon transfer have provided significant insight into muscle adaptation in vivo. Yet, to date, there is no mathematical model that allows us to predict how skeletal muscle adapts to mechanical stretch in silico. Here we propose a novel mechanistic model for chronic longitudinal muscle growth in response to passive mechanical stretch. We characterize growth through a single scalar-valued internal variable, the serial sarcomere number. Sarcomerogenesis, the evolution of this variable, is driven by the elastic mechanical stretch. To analyze realistic three-dimensional muscle geometries, we embed our model into a nonlinear finite element framework. In a chronic limb lengthening study with a muscle stretch of 1.14, the model predicts an acute sarcomere lengthening from 3.09[Image: see text]m to 3.51[Image: see text]m, and a chronic gradual return to the initial sarcomere length within two weeks. Compared to the experiment, the acute model error was 0.00% by design of the model; the chronic model error was 2.13%, which lies within the rage of the experimental standard deviation. Our model explains, from a mechanistic point of view, why gradual multi-step muscle lengthening is less invasive than single-step lengthening. It also explains regional variations in sarcomere length, shorter close to and longer away from the muscle-tendon interface. Once calibrated with a richer data set, our model may help surgeons to prevent muscle overstretch and make informed decisions about optimal stretch increments, stretch timing, and stretch amplitudes. We anticipate our study to open new avenues in orthopedic and reconstructive surgery and enhance treatment for patients with ill proportioned limbs, tendon lengthening, tendon transfer, tendon tear, and chronically retracted muscles.
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spelling pubmed-34622002012-10-05 Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis Zöllner, Alexander M. Abilez, Oscar J. Böl, Markus Kuhl, Ellen PLoS One Research Article Skeletal muscle responds to passive overstretch through sarcomerogenesis, the creation and serial deposition of new sarcomere units. Sarcomerogenesis is critical to muscle function: It gradually re-positions the muscle back into its optimal operating regime. Animal models of immobilization, limb lengthening, and tendon transfer have provided significant insight into muscle adaptation in vivo. Yet, to date, there is no mathematical model that allows us to predict how skeletal muscle adapts to mechanical stretch in silico. Here we propose a novel mechanistic model for chronic longitudinal muscle growth in response to passive mechanical stretch. We characterize growth through a single scalar-valued internal variable, the serial sarcomere number. Sarcomerogenesis, the evolution of this variable, is driven by the elastic mechanical stretch. To analyze realistic three-dimensional muscle geometries, we embed our model into a nonlinear finite element framework. In a chronic limb lengthening study with a muscle stretch of 1.14, the model predicts an acute sarcomere lengthening from 3.09[Image: see text]m to 3.51[Image: see text]m, and a chronic gradual return to the initial sarcomere length within two weeks. Compared to the experiment, the acute model error was 0.00% by design of the model; the chronic model error was 2.13%, which lies within the rage of the experimental standard deviation. Our model explains, from a mechanistic point of view, why gradual multi-step muscle lengthening is less invasive than single-step lengthening. It also explains regional variations in sarcomere length, shorter close to and longer away from the muscle-tendon interface. Once calibrated with a richer data set, our model may help surgeons to prevent muscle overstretch and make informed decisions about optimal stretch increments, stretch timing, and stretch amplitudes. We anticipate our study to open new avenues in orthopedic and reconstructive surgery and enhance treatment for patients with ill proportioned limbs, tendon lengthening, tendon transfer, tendon tear, and chronically retracted muscles. Public Library of Science 2012-10-01 /pmc/articles/PMC3462200/ /pubmed/23049683 http://dx.doi.org/10.1371/journal.pone.0045661 Text en © 2012 Zöllner et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zöllner, Alexander M.
Abilez, Oscar J.
Böl, Markus
Kuhl, Ellen
Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title_full Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title_fullStr Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title_full_unstemmed Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title_short Stretching Skeletal Muscle: Chronic Muscle Lengthening through Sarcomerogenesis
title_sort stretching skeletal muscle: chronic muscle lengthening through sarcomerogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462200/
https://www.ncbi.nlm.nih.gov/pubmed/23049683
http://dx.doi.org/10.1371/journal.pone.0045661
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