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Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats

To investigate whether the administration frequency of parathyroid hormone (PTH) is associated with the development of cortical porosity, this study established 15 dosage regimens of teriparatide [human PTH(1–34), TPTD] with four distinct concentrations and four distinct administration frequencies o...

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Autores principales: Takakura, Aya, Lee, Ji-Won, Hirano, Kyoko, Isogai, Yukihiro, Ishizuya, Toshinori, Takao-Kawabata, Ryoko, Iimura, Tadahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405404/
https://www.ncbi.nlm.nih.gov/pubmed/28503340
http://dx.doi.org/10.1038/boneres.2017.2
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author Takakura, Aya
Lee, Ji-Won
Hirano, Kyoko
Isogai, Yukihiro
Ishizuya, Toshinori
Takao-Kawabata, Ryoko
Iimura, Tadahiro
author_facet Takakura, Aya
Lee, Ji-Won
Hirano, Kyoko
Isogai, Yukihiro
Ishizuya, Toshinori
Takao-Kawabata, Ryoko
Iimura, Tadahiro
author_sort Takakura, Aya
collection PubMed
description To investigate whether the administration frequency of parathyroid hormone (PTH) is associated with the development of cortical porosity, this study established 15 dosage regimens of teriparatide [human PTH(1–34), TPTD] with four distinct concentrations and four distinct administration frequencies of TPTD to 16-week-old ovariectomized rats. Our analyses demonstrated that the bone mineral density, mechanical properties, and bone turnover were associated with the total amount of TPTD administered. Our observations further revealed that the cortical porosity was markedly developed as a result of an increased administration frequency with a lower concentration of total TPTD administration in our setting, although the highest concentration also induced cortical porosity. Deconvolution fluorescence tiling imaging on calcein-labeled undecalcified bone sections also demonstrated the development of cortical porosity to be closely associated with the bone site where periosteal bone formation took place. This site-specific cortical porosity involved intracortical bone resorption and an increased number and proximity of osteocytic lacunae, occasionally causing fused lacunae. Taken together, these findings suggested the involvement of local distinctions in the rate of bone growth that may be related to the site-specific mechanical properties in the development of cortical porosity induced by frequent and/or high doses of TPTD.
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spelling pubmed-54054042017-05-12 Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats Takakura, Aya Lee, Ji-Won Hirano, Kyoko Isogai, Yukihiro Ishizuya, Toshinori Takao-Kawabata, Ryoko Iimura, Tadahiro Bone Res Article To investigate whether the administration frequency of parathyroid hormone (PTH) is associated with the development of cortical porosity, this study established 15 dosage regimens of teriparatide [human PTH(1–34), TPTD] with four distinct concentrations and four distinct administration frequencies of TPTD to 16-week-old ovariectomized rats. Our analyses demonstrated that the bone mineral density, mechanical properties, and bone turnover were associated with the total amount of TPTD administered. Our observations further revealed that the cortical porosity was markedly developed as a result of an increased administration frequency with a lower concentration of total TPTD administration in our setting, although the highest concentration also induced cortical porosity. Deconvolution fluorescence tiling imaging on calcein-labeled undecalcified bone sections also demonstrated the development of cortical porosity to be closely associated with the bone site where periosteal bone formation took place. This site-specific cortical porosity involved intracortical bone resorption and an increased number and proximity of osteocytic lacunae, occasionally causing fused lacunae. Taken together, these findings suggested the involvement of local distinctions in the rate of bone growth that may be related to the site-specific mechanical properties in the development of cortical porosity induced by frequent and/or high doses of TPTD. Nature Publishing Group 2017-04-25 /pmc/articles/PMC5405404/ /pubmed/28503340 http://dx.doi.org/10.1038/boneres.2017.2 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Takakura, Aya
Lee, Ji-Won
Hirano, Kyoko
Isogai, Yukihiro
Ishizuya, Toshinori
Takao-Kawabata, Ryoko
Iimura, Tadahiro
Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title_full Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title_fullStr Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title_full_unstemmed Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title_short Administration frequency as well as dosage of PTH are associated with development of cortical porosity in ovariectomized rats
title_sort administration frequency as well as dosage of pth are associated with development of cortical porosity in ovariectomized rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405404/
https://www.ncbi.nlm.nih.gov/pubmed/28503340
http://dx.doi.org/10.1038/boneres.2017.2
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