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Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization

Owing to their cursorial background, ostriches (Struthio camelus) walk and run with high metabolic economy, can reach very fast running speeds and quickly execute cutting manoeuvres. These capabilities are believed to be a result of their ability to coordinate muscles to take advantage of specialize...

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Detalles Bibliográficos
Autores principales: Rankin, Jeffery W., Rubenson, Jonas, Hutchinson, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892259/
https://www.ncbi.nlm.nih.gov/pubmed/27146688
http://dx.doi.org/10.1098/rsif.2016.0035
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author Rankin, Jeffery W.
Rubenson, Jonas
Hutchinson, John R.
author_facet Rankin, Jeffery W.
Rubenson, Jonas
Hutchinson, John R.
author_sort Rankin, Jeffery W.
collection PubMed
description Owing to their cursorial background, ostriches (Struthio camelus) walk and run with high metabolic economy, can reach very fast running speeds and quickly execute cutting manoeuvres. These capabilities are believed to be a result of their ability to coordinate muscles to take advantage of specialized passive limb structures. This study aimed to infer the functional roles of ostrich pelvic limb muscles during gait. Existing gait data were combined with a newly developed musculoskeletal model to generate simulations of ostrich walking and running that predict muscle excitations, force and mechanical work. Consistent with previous avian electromyography studies, predicted excitation patterns showed that individual muscles tended to be excited primarily during only stance or swing. Work and force estimates show that ostrich gaits are partially hip-driven with the bi-articular hip–knee muscles driving stance mechanics. Conversely, the knee extensors acted as brakes, absorbing energy. The digital extensors generated large amounts of both negative and positive mechanical work, with increased magnitudes during running, providing further evidence that ostriches make extensive use of tendinous elastic energy storage to improve economy. The simulations also highlight the need to carefully consider non-muscular soft tissues that may play a role in ostrich gait.
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spelling pubmed-48922592016-06-08 Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization Rankin, Jeffery W. Rubenson, Jonas Hutchinson, John R. J R Soc Interface Life Sciences–Engineering interface Owing to their cursorial background, ostriches (Struthio camelus) walk and run with high metabolic economy, can reach very fast running speeds and quickly execute cutting manoeuvres. These capabilities are believed to be a result of their ability to coordinate muscles to take advantage of specialized passive limb structures. This study aimed to infer the functional roles of ostrich pelvic limb muscles during gait. Existing gait data were combined with a newly developed musculoskeletal model to generate simulations of ostrich walking and running that predict muscle excitations, force and mechanical work. Consistent with previous avian electromyography studies, predicted excitation patterns showed that individual muscles tended to be excited primarily during only stance or swing. Work and force estimates show that ostrich gaits are partially hip-driven with the bi-articular hip–knee muscles driving stance mechanics. Conversely, the knee extensors acted as brakes, absorbing energy. The digital extensors generated large amounts of both negative and positive mechanical work, with increased magnitudes during running, providing further evidence that ostriches make extensive use of tendinous elastic energy storage to improve economy. The simulations also highlight the need to carefully consider non-muscular soft tissues that may play a role in ostrich gait. The Royal Society 2016-05 /pmc/articles/PMC4892259/ /pubmed/27146688 http://dx.doi.org/10.1098/rsif.2016.0035 Text en © 2016 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 Life Sciences–Engineering interface
Rankin, Jeffery W.
Rubenson, Jonas
Hutchinson, John R.
Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title_full Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title_fullStr Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title_full_unstemmed Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title_short Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
title_sort inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization
topic Life Sciences–Engineering interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892259/
https://www.ncbi.nlm.nih.gov/pubmed/27146688
http://dx.doi.org/10.1098/rsif.2016.0035
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