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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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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. |
format | Online Article Text |
id | pubmed-4892259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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