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Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot
The central nervous system utilizes tendon compliance of the intrinsic foot muscles to aid the foot's arch spring, storing and returning energy in its tendinous tissues. Recently, the intrinsic foot muscles have been shown to adapt their energetic contributions during a variety of locomotor tas...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124483/ https://www.ncbi.nlm.nih.gov/pubmed/35344050 http://dx.doi.org/10.1242/jeb.243792 |
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author | Smith, Ross E. Lichtwark, Glen A. Kelly, Luke A. |
author_facet | Smith, Ross E. Lichtwark, Glen A. Kelly, Luke A. |
author_sort | Smith, Ross E. |
collection | PubMed |
description | The central nervous system utilizes tendon compliance of the intrinsic foot muscles to aid the foot's arch spring, storing and returning energy in its tendinous tissues. Recently, the intrinsic foot muscles have been shown to adapt their energetic contributions during a variety of locomotor tasks to fulfil centre of mass work demands. However, the mechanism by which the small intrinsic foot muscles are able to make versatile energetic contributions remains unknown. Therefore, we examined the muscle–tendon dynamics of the flexor digitorum brevis during stepping, jumping and landing tasks to see whether the central nervous system regulates muscle activation magnitude and timing to enable energy storage and return to enhance energetic contributions. In step-ups and jumps, energy was stored in the tendinous tissue during arch compression; during arch recoil, the fascicles shortened at a slower rate than the tendinous tissues while the foot generated energy. In step-downs and landings, the tendinous tissues elongated more and at greater rates than the fascicles during arch compression while the foot absorbed energy. These results indicate that the central nervous system utilizes arch compression to store elastic energy in the tendinous tissues of the intrinsic foot muscles to add or remove mechanical energy when the body accelerates or decelerates. This study provides evidence for an adaptive mechanism to enable the foot's energetic versatility and further indicates the value of tendon compliance in distal lower limb muscle–tendon units in locomotion. |
format | Online Article Text |
id | pubmed-9124483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-91244832022-06-04 Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot Smith, Ross E. Lichtwark, Glen A. Kelly, Luke A. J Exp Biol Research Article The central nervous system utilizes tendon compliance of the intrinsic foot muscles to aid the foot's arch spring, storing and returning energy in its tendinous tissues. Recently, the intrinsic foot muscles have been shown to adapt their energetic contributions during a variety of locomotor tasks to fulfil centre of mass work demands. However, the mechanism by which the small intrinsic foot muscles are able to make versatile energetic contributions remains unknown. Therefore, we examined the muscle–tendon dynamics of the flexor digitorum brevis during stepping, jumping and landing tasks to see whether the central nervous system regulates muscle activation magnitude and timing to enable energy storage and return to enhance energetic contributions. In step-ups and jumps, energy was stored in the tendinous tissue during arch compression; during arch recoil, the fascicles shortened at a slower rate than the tendinous tissues while the foot generated energy. In step-downs and landings, the tendinous tissues elongated more and at greater rates than the fascicles during arch compression while the foot absorbed energy. These results indicate that the central nervous system utilizes arch compression to store elastic energy in the tendinous tissues of the intrinsic foot muscles to add or remove mechanical energy when the body accelerates or decelerates. This study provides evidence for an adaptive mechanism to enable the foot's energetic versatility and further indicates the value of tendon compliance in distal lower limb muscle–tendon units in locomotion. The Company of Biologists Ltd 2022-04-22 /pmc/articles/PMC9124483/ /pubmed/35344050 http://dx.doi.org/10.1242/jeb.243792 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Smith, Ross E. Lichtwark, Glen A. Kelly, Luke A. Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title | Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title_full | Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title_fullStr | Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title_full_unstemmed | Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title_short | Flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
title_sort | flexor digitorum brevis utilizes elastic strain energy to contribute to both work generation and energy absorption at the foot |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124483/ https://www.ncbi.nlm.nih.gov/pubmed/35344050 http://dx.doi.org/10.1242/jeb.243792 |
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