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Effects of eldecalcitol on cortical bone response to mechanical loading in rats
BACKGROUND: Mechanical loading of bones activates modeling and suppresses remodeling by promoting bone formation. Eldecalcitol is approved for the treatment of osteoporosis in Japan and is often used in patients undergoing exercise therapy. However, the effects of eldecalcitol on bone formation duri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484892/ https://www.ncbi.nlm.nih.gov/pubmed/26123128 http://dx.doi.org/10.1186/s12891-015-0613-3 |
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author | Yamasaki, Yusuke Nagira, Keita Osaki, Mari Nagashima, Hideki Hagino, Hiroshi |
author_facet | Yamasaki, Yusuke Nagira, Keita Osaki, Mari Nagashima, Hideki Hagino, Hiroshi |
author_sort | Yamasaki, Yusuke |
collection | PubMed |
description | BACKGROUND: Mechanical loading of bones activates modeling and suppresses remodeling by promoting bone formation. Eldecalcitol is approved for the treatment of osteoporosis in Japan and is often used in patients undergoing exercise therapy. However, the effects of eldecalcitol on bone formation during mechanical loading are unknown. The aim of this study was to clarify the influence of eldecalcitol administration on bone response to mechanical loading using a four-point bending device. METHODS: Forty six-month-old female Wistar rats were randomized into four groups based on eldecalcitol dose (vehicle administration (VEH), low dose (ED-L), medium dose (ED-M), and high dose (ED-H)). Loads of 38 N were applied in vivo to the right tibia for 36 cycles at 2 Hz, by four-point bending, 3 days per week for 3 weeks. After calcein double-labeling, rats were sacrificed and tibial cross sections were prepared from the region with maximal bending at the central diaphysis. Histomorphometry was performed on the entire periosteal and endocortical surface of the tibiae, dividing the periosteum into lateral and medial surfaces. RESULTS: The effects of external loading on bone formation parameters were significant at all three surfaces. Bone formation parameters were highest in the ED-H group, and the effects of eldecalcitol on bone formation rate were significant at the endocortical surface. In addition, the interaction between loading and eldecalcitol dose significantly affected bone formation rate at the endocortical surface. CONCLUSIONS: Eldecalcitol enhanced the cortical bone response to mechanical loading and a synergistic effect was observed in a rat model. |
format | Online Article Text |
id | pubmed-4484892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44848922015-06-30 Effects of eldecalcitol on cortical bone response to mechanical loading in rats Yamasaki, Yusuke Nagira, Keita Osaki, Mari Nagashima, Hideki Hagino, Hiroshi BMC Musculoskelet Disord Research Article BACKGROUND: Mechanical loading of bones activates modeling and suppresses remodeling by promoting bone formation. Eldecalcitol is approved for the treatment of osteoporosis in Japan and is often used in patients undergoing exercise therapy. However, the effects of eldecalcitol on bone formation during mechanical loading are unknown. The aim of this study was to clarify the influence of eldecalcitol administration on bone response to mechanical loading using a four-point bending device. METHODS: Forty six-month-old female Wistar rats were randomized into four groups based on eldecalcitol dose (vehicle administration (VEH), low dose (ED-L), medium dose (ED-M), and high dose (ED-H)). Loads of 38 N were applied in vivo to the right tibia for 36 cycles at 2 Hz, by four-point bending, 3 days per week for 3 weeks. After calcein double-labeling, rats were sacrificed and tibial cross sections were prepared from the region with maximal bending at the central diaphysis. Histomorphometry was performed on the entire periosteal and endocortical surface of the tibiae, dividing the periosteum into lateral and medial surfaces. RESULTS: The effects of external loading on bone formation parameters were significant at all three surfaces. Bone formation parameters were highest in the ED-H group, and the effects of eldecalcitol on bone formation rate were significant at the endocortical surface. In addition, the interaction between loading and eldecalcitol dose significantly affected bone formation rate at the endocortical surface. CONCLUSIONS: Eldecalcitol enhanced the cortical bone response to mechanical loading and a synergistic effect was observed in a rat model. BioMed Central 2015-06-30 /pmc/articles/PMC4484892/ /pubmed/26123128 http://dx.doi.org/10.1186/s12891-015-0613-3 Text en © Yamasaki et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yamasaki, Yusuke Nagira, Keita Osaki, Mari Nagashima, Hideki Hagino, Hiroshi Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title | Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title_full | Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title_fullStr | Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title_full_unstemmed | Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title_short | Effects of eldecalcitol on cortical bone response to mechanical loading in rats |
title_sort | effects of eldecalcitol on cortical bone response to mechanical loading in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484892/ https://www.ncbi.nlm.nih.gov/pubmed/26123128 http://dx.doi.org/10.1186/s12891-015-0613-3 |
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