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Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium
BACKGROUND: The role of selenium (Se) on bone microarchitecture is still poorly understood. The present study aims to investigate the macroscopic and microscopic structures of femoral bone tissue in adult male rats after subchronic peroral administration of Se. METHODS: Twenty one-month-old male Wis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598879/ https://www.ncbi.nlm.nih.gov/pubmed/23369508 http://dx.doi.org/10.1186/1751-0147-55-8 |
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author | Martiniaková, Monika Boboňová, Ivana Omelka, Radoslav Grosskopf, Birgit Stawarz, Robert Toman, Róbert |
author_facet | Martiniaková, Monika Boboňová, Ivana Omelka, Radoslav Grosskopf, Birgit Stawarz, Robert Toman, Róbert |
author_sort | Martiniaková, Monika |
collection | PubMed |
description | BACKGROUND: The role of selenium (Se) on bone microarchitecture is still poorly understood. The present study aims to investigate the macroscopic and microscopic structures of femoral bone tissue in adult male rats after subchronic peroral administration of Se. METHODS: Twenty one-month-old male Wistar rats were randomly divided into two experimental groups. In the first group (Se group) young males were exposed to 5 mg Na(2)SeO(3)/L in drinking water, for 90 days. Ten one-month-old males without Se administration served as a control group. At the end of the experiment, macroscopic and microscopic structures of the femurs were analysed using analytical scales, sliding instrument, and polarized light microscopy. RESULTS: The body weight, femoral length and cortical bone thickness were significantly decreased in Se group rats. These rats also displayed different microstructure in the middle part of the femur, both in medial and lateral views, where vascular canals expanded into the central area of the bone while, in control rats, these canals occurred only near the endosteal surfaces. Additionally, a smaller number of primary and secondary osteons was identified in Se group rats. Histomorphometric analyses revealed significant increases for area, perimeter, maximum and minimum diameters of primary osteons’ vascular canals but significant reductions for all measured variables of Haversian canals and secondary osteons. CONCLUSIONS: Se negatively affected the macroscopic and microscopic structures of femoral bone tissue in adult male rats. The results contribute to the knowledge on damaging impact of Se on bone. |
format | Online Article Text |
id | pubmed-3598879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35988792013-03-17 Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium Martiniaková, Monika Boboňová, Ivana Omelka, Radoslav Grosskopf, Birgit Stawarz, Robert Toman, Róbert Acta Vet Scand Research BACKGROUND: The role of selenium (Se) on bone microarchitecture is still poorly understood. The present study aims to investigate the macroscopic and microscopic structures of femoral bone tissue in adult male rats after subchronic peroral administration of Se. METHODS: Twenty one-month-old male Wistar rats were randomly divided into two experimental groups. In the first group (Se group) young males were exposed to 5 mg Na(2)SeO(3)/L in drinking water, for 90 days. Ten one-month-old males without Se administration served as a control group. At the end of the experiment, macroscopic and microscopic structures of the femurs were analysed using analytical scales, sliding instrument, and polarized light microscopy. RESULTS: The body weight, femoral length and cortical bone thickness were significantly decreased in Se group rats. These rats also displayed different microstructure in the middle part of the femur, both in medial and lateral views, where vascular canals expanded into the central area of the bone while, in control rats, these canals occurred only near the endosteal surfaces. Additionally, a smaller number of primary and secondary osteons was identified in Se group rats. Histomorphometric analyses revealed significant increases for area, perimeter, maximum and minimum diameters of primary osteons’ vascular canals but significant reductions for all measured variables of Haversian canals and secondary osteons. CONCLUSIONS: Se negatively affected the macroscopic and microscopic structures of femoral bone tissue in adult male rats. The results contribute to the knowledge on damaging impact of Se on bone. BioMed Central 2013-02-01 /pmc/articles/PMC3598879/ /pubmed/23369508 http://dx.doi.org/10.1186/1751-0147-55-8 Text en Copyright ©2013 Martiniaková et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Martiniaková, Monika Boboňová, Ivana Omelka, Radoslav Grosskopf, Birgit Stawarz, Robert Toman, Róbert Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title | Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title_full | Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title_fullStr | Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title_full_unstemmed | Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title_short | Structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
title_sort | structural changes in femoral bone tissue of rats after subchronic peroral exposure to selenium |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598879/ https://www.ncbi.nlm.nih.gov/pubmed/23369508 http://dx.doi.org/10.1186/1751-0147-55-8 |
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