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Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT
SUMMARY: Using in vivo microcomputed tomography (micro-CT), we found in parathyroid hormone (PTH)-treated osteopenic rats linear increases in cortical and trabecular, due to increased trabecular thickness and number, bone mass. Bone was formed in cavities, leading to restoral of nearly cleaved trabe...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765647/ https://www.ncbi.nlm.nih.gov/pubmed/19262974 http://dx.doi.org/10.1007/s00198-009-0882-5 |
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author | Brouwers, J. E. M. van Rietbergen, B. Huiskes, R. Ito, K. |
author_facet | Brouwers, J. E. M. van Rietbergen, B. Huiskes, R. Ito, K. |
author_sort | Brouwers, J. E. M. |
collection | PubMed |
description | SUMMARY: Using in vivo microcomputed tomography (micro-CT), we found in parathyroid hormone (PTH)-treated osteopenic rats linear increases in cortical and trabecular, due to increased trabecular thickness and number, bone mass. Bone was formed in cavities, leading to restoral of nearly cleaved trabeculae. For the first time, effects in PTH-treated rats were analyzed longitudinally. INTRODUCTION: Our aims were to over time (1) determine changes in trabecular thickness and number after PTH, (2) compare responses to PTH between the meta- and epiphysis, (3) determine effects of PTH on mineralization and mechanical properties, (4) determine locations of new bone formation due to PTH on a microlevel, and (5) determine the predictive value of bone structural properties for gain in bone mass after PTH. METHODS: Adult rats were divided into ovariectomy (OVX; n = 8), SHAM-OVX (n = 8), and OVX and PTH treatment (n = 9). Between weeks 8 and 14, PTH rats received daily subcutaneous PTH injections (60 μg/kg/day). At weeks 0, 8, 10, 12, and 14, in vivo micro-CT scans were made of the proximal and diaphyseal tibia. After sacrifice, all tibiae were tested in three-point bending. RESULTS: PTH increased bone volume fraction linearly over time in meta- and epiphysis, accompanied by increased trabecular thickness in both and increased trabecular number only in the latter one. CT-estimated mineralization increased in trabecular and remained constant in cortical bone. Ultimate load and energy were increased and ultimate displacement and stiffness unaltered compared to SHAM rats. For those trabeculae analyzed, bone was formed initially on places where it was most beneficial for increasing their strength and later on to all surfaces. |
format | Text |
id | pubmed-2765647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27656472009-10-23 Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT Brouwers, J. E. M. van Rietbergen, B. Huiskes, R. Ito, K. Osteoporos Int Original Article SUMMARY: Using in vivo microcomputed tomography (micro-CT), we found in parathyroid hormone (PTH)-treated osteopenic rats linear increases in cortical and trabecular, due to increased trabecular thickness and number, bone mass. Bone was formed in cavities, leading to restoral of nearly cleaved trabeculae. For the first time, effects in PTH-treated rats were analyzed longitudinally. INTRODUCTION: Our aims were to over time (1) determine changes in trabecular thickness and number after PTH, (2) compare responses to PTH between the meta- and epiphysis, (3) determine effects of PTH on mineralization and mechanical properties, (4) determine locations of new bone formation due to PTH on a microlevel, and (5) determine the predictive value of bone structural properties for gain in bone mass after PTH. METHODS: Adult rats were divided into ovariectomy (OVX; n = 8), SHAM-OVX (n = 8), and OVX and PTH treatment (n = 9). Between weeks 8 and 14, PTH rats received daily subcutaneous PTH injections (60 μg/kg/day). At weeks 0, 8, 10, 12, and 14, in vivo micro-CT scans were made of the proximal and diaphyseal tibia. After sacrifice, all tibiae were tested in three-point bending. RESULTS: PTH increased bone volume fraction linearly over time in meta- and epiphysis, accompanied by increased trabecular thickness in both and increased trabecular number only in the latter one. CT-estimated mineralization increased in trabecular and remained constant in cortical bone. Ultimate load and energy were increased and ultimate displacement and stiffness unaltered compared to SHAM rats. For those trabeculae analyzed, bone was formed initially on places where it was most beneficial for increasing their strength and later on to all surfaces. Springer-Verlag 2009-03-05 2009 /pmc/articles/PMC2765647/ /pubmed/19262974 http://dx.doi.org/10.1007/s00198-009-0882-5 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Brouwers, J. E. M. van Rietbergen, B. Huiskes, R. Ito, K. Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title | Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title_full | Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title_fullStr | Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title_full_unstemmed | Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title_short | Effects of PTH treatment on tibial bone of ovariectomized rats assessed by in vivo micro-CT |
title_sort | effects of pth treatment on tibial bone of ovariectomized rats assessed by in vivo micro-ct |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765647/ https://www.ncbi.nlm.nih.gov/pubmed/19262974 http://dx.doi.org/10.1007/s00198-009-0882-5 |
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