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Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running

The phenotypic response of bones differing in morphological, compositional, and mechanical traits to an increase in loading during growth is not well understood. We tested whether bones of two inbred mouse strains that assemble differing sets of traits to achieve mechanical homeostasis at adulthood...

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Autores principales: Schlecht, Stephen H., Ramcharan, Melissa A., Yang, Yueqin, Smith, Lauren M, Bigelow, Erin MR, Nolan, Bonnie T, Moss, Drew E, Devlin, Maureen J, Jepsen, Karl J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124195/
https://www.ncbi.nlm.nih.gov/pubmed/30283899
http://dx.doi.org/10.1002/jbm4.10032
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author Schlecht, Stephen H.
Ramcharan, Melissa A.
Yang, Yueqin
Smith, Lauren M
Bigelow, Erin MR
Nolan, Bonnie T
Moss, Drew E
Devlin, Maureen J
Jepsen, Karl J
author_facet Schlecht, Stephen H.
Ramcharan, Melissa A.
Yang, Yueqin
Smith, Lauren M
Bigelow, Erin MR
Nolan, Bonnie T
Moss, Drew E
Devlin, Maureen J
Jepsen, Karl J
author_sort Schlecht, Stephen H.
collection PubMed
description The phenotypic response of bones differing in morphological, compositional, and mechanical traits to an increase in loading during growth is not well understood. We tested whether bones of two inbred mouse strains that assemble differing sets of traits to achieve mechanical homeostasis at adulthood would show divergent responses to voluntary cage‐wheel running. Female A/J and C57BL6/J (B6) 4‐week‐old mice were provided unrestricted access to a standard cage‐wheel for 4 weeks. A/J mice have narrow and highly mineralized femora and B6 mice have wide and less mineralized femora. Both strains averaged 2 to 9.5 km of running per day, with the average‐distance run between strains not significantly different (p = 0.133). Exercised A/J femora showed an anabolic response to exercise with the diaphyses showing a 2.8% greater total area (Tt.Ar, p = 0.06) and 4.7% greater cortical area (Ct.Ar, p = 0.012) compared to controls. In contrast, exercised B6 femora showed a 6.2% (p < 0.001) decrease in Tt.Ar (p < 0.001) and a 6.7% decrease in Ct.Ar (p = 0.133) compared to controls, with the femora showing significant marrow infilling (p = 0.002). These divergent morphological responses to exercise, which did not depend on the daily distance run, translated to a 7.9% (p = 0.001) higher maximum load (ML) for exercised A/J femora but no change in ML for exercised B6 femora compared to controls. A consistent response was observed for the humeri but not the vertebral bodies. This differential outcome to exercise has not been previously observed in isolated loading or forced treadmill running regimes. Our findings suggest there are critical factors involved in the metabolic response to exercise during growth that require further consideration to understand how genotype, exercise, bone morphology, and whole‐bone strength interact during growth. © 2018 The Authors. JBMR Plus is published by Wiley Periodicals, Inc. on behalf of the American Society for Bone and Mineral Research.
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spelling pubmed-61241952018-10-03 Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running Schlecht, Stephen H. Ramcharan, Melissa A. Yang, Yueqin Smith, Lauren M Bigelow, Erin MR Nolan, Bonnie T Moss, Drew E Devlin, Maureen J Jepsen, Karl J JBMR Plus Original Articles The phenotypic response of bones differing in morphological, compositional, and mechanical traits to an increase in loading during growth is not well understood. We tested whether bones of two inbred mouse strains that assemble differing sets of traits to achieve mechanical homeostasis at adulthood would show divergent responses to voluntary cage‐wheel running. Female A/J and C57BL6/J (B6) 4‐week‐old mice were provided unrestricted access to a standard cage‐wheel for 4 weeks. A/J mice have narrow and highly mineralized femora and B6 mice have wide and less mineralized femora. Both strains averaged 2 to 9.5 km of running per day, with the average‐distance run between strains not significantly different (p = 0.133). Exercised A/J femora showed an anabolic response to exercise with the diaphyses showing a 2.8% greater total area (Tt.Ar, p = 0.06) and 4.7% greater cortical area (Ct.Ar, p = 0.012) compared to controls. In contrast, exercised B6 femora showed a 6.2% (p < 0.001) decrease in Tt.Ar (p < 0.001) and a 6.7% decrease in Ct.Ar (p = 0.133) compared to controls, with the femora showing significant marrow infilling (p = 0.002). These divergent morphological responses to exercise, which did not depend on the daily distance run, translated to a 7.9% (p = 0.001) higher maximum load (ML) for exercised A/J femora but no change in ML for exercised B6 femora compared to controls. A consistent response was observed for the humeri but not the vertebral bodies. This differential outcome to exercise has not been previously observed in isolated loading or forced treadmill running regimes. Our findings suggest there are critical factors involved in the metabolic response to exercise during growth that require further consideration to understand how genotype, exercise, bone morphology, and whole‐bone strength interact during growth. © 2018 The Authors. JBMR Plus is published by Wiley Periodicals, Inc. on behalf of the American Society for Bone and Mineral Research. John Wiley and Sons Inc. 2018-02-12 /pmc/articles/PMC6124195/ /pubmed/30283899 http://dx.doi.org/10.1002/jbm4.10032 Text en © 2018 The Authors. JBMR Plus is published by Wiley Periodicals, Inc. on behalf of the American Society for Bone and Mineral Research This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Schlecht, Stephen H.
Ramcharan, Melissa A.
Yang, Yueqin
Smith, Lauren M
Bigelow, Erin MR
Nolan, Bonnie T
Moss, Drew E
Devlin, Maureen J
Jepsen, Karl J
Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title_full Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title_fullStr Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title_full_unstemmed Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title_short Differential Adaptive Response of Growing Bones From Two Female Inbred Mouse Strains to Voluntary Cage‐Wheel Running
title_sort differential adaptive response of growing bones from two female inbred mouse strains to voluntary cage‐wheel running
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124195/
https://www.ncbi.nlm.nih.gov/pubmed/30283899
http://dx.doi.org/10.1002/jbm4.10032
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