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Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response

Mechanoadaptation maintains bone mass and architecture; its failure underlies age-related decline in bone strength. It is unclear whether this is due to failure of osteocytes to sense strain, osteoblasts to form bone or insufficient mechanical stimulus. Mechanoadaptation can be restored to aged bone...

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Autores principales: Javaheri, Behzad, Carriero, Alessandra, Wood, Maria, De Souza, Roberto, Lee, Peter D., Shefelbine, Sandra, Pitsillides, Andrew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5924380/
https://www.ncbi.nlm.nih.gov/pubmed/29703931
http://dx.doi.org/10.1038/s41598-018-25084-6
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author Javaheri, Behzad
Carriero, Alessandra
Wood, Maria
De Souza, Roberto
Lee, Peter D.
Shefelbine, Sandra
Pitsillides, Andrew A.
author_facet Javaheri, Behzad
Carriero, Alessandra
Wood, Maria
De Souza, Roberto
Lee, Peter D.
Shefelbine, Sandra
Pitsillides, Andrew A.
author_sort Javaheri, Behzad
collection PubMed
description Mechanoadaptation maintains bone mass and architecture; its failure underlies age-related decline in bone strength. It is unclear whether this is due to failure of osteocytes to sense strain, osteoblasts to form bone or insufficient mechanical stimulus. Mechanoadaptation can be restored to aged bone by surgical neurectomy, suggesting that changes in loading history can rescue mechanoadaptation. We use non-biased, whole-bone tibial analyses, along with characterisation of surface strains and ensuing mechanoadaptive responses in mice at a range of ages, to explore whether sufficient load magnitude can activate mechanoadaptation in aged bone. We find that younger mice adapt when imposed strains are lower than in mature and aged bone. Intriguingly, imposition of short-term, high magnitude loading effectively primes cortical but not trabecular bone of aged mice to respond. This response was regionally-matched to highest strains measured by digital image correlation and to osteocytic mechanoactivation. These data indicate that aged bone’s loading response can be partially recovered, non-invasively by transient, focal high strain regions. Our results indicate that old murine bone does respond to load when the loading is of sufficient magnitude, and bones’ age-related adaptation failure may be due to insufficient mechanical stimulus to trigger mechanoadaptation.
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spelling pubmed-59243802018-05-01 Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response Javaheri, Behzad Carriero, Alessandra Wood, Maria De Souza, Roberto Lee, Peter D. Shefelbine, Sandra Pitsillides, Andrew A. Sci Rep Article Mechanoadaptation maintains bone mass and architecture; its failure underlies age-related decline in bone strength. It is unclear whether this is due to failure of osteocytes to sense strain, osteoblasts to form bone or insufficient mechanical stimulus. Mechanoadaptation can be restored to aged bone by surgical neurectomy, suggesting that changes in loading history can rescue mechanoadaptation. We use non-biased, whole-bone tibial analyses, along with characterisation of surface strains and ensuing mechanoadaptive responses in mice at a range of ages, to explore whether sufficient load magnitude can activate mechanoadaptation in aged bone. We find that younger mice adapt when imposed strains are lower than in mature and aged bone. Intriguingly, imposition of short-term, high magnitude loading effectively primes cortical but not trabecular bone of aged mice to respond. This response was regionally-matched to highest strains measured by digital image correlation and to osteocytic mechanoactivation. These data indicate that aged bone’s loading response can be partially recovered, non-invasively by transient, focal high strain regions. Our results indicate that old murine bone does respond to load when the loading is of sufficient magnitude, and bones’ age-related adaptation failure may be due to insufficient mechanical stimulus to trigger mechanoadaptation. Nature Publishing Group UK 2018-04-27 /pmc/articles/PMC5924380/ /pubmed/29703931 http://dx.doi.org/10.1038/s41598-018-25084-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Javaheri, Behzad
Carriero, Alessandra
Wood, Maria
De Souza, Roberto
Lee, Peter D.
Shefelbine, Sandra
Pitsillides, Andrew A.
Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title_full Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title_fullStr Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title_full_unstemmed Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title_short Transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
title_sort transient peak-strain matching partially recovers the age-impaired mechanoadaptive cortical bone response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5924380/
https://www.ncbi.nlm.nih.gov/pubmed/29703931
http://dx.doi.org/10.1038/s41598-018-25084-6
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