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Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding
BACKGROUND: The most prominent features of hypervitaminosis A in rats are spontaneous fractures and anorexia. Since caloric restriction induces alterations in bone, some effects could be secondary to loss of appetite. To clarify the mechanisms behind vitamin A-induced bone fragility it is necessary...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055747/ https://www.ncbi.nlm.nih.gov/pubmed/29697007 http://dx.doi.org/10.1080/03009734.2018.1448020 |
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author | Lind, Thomas Lind, P. Monica Hu, Lijuan Melhus, Håkan |
author_facet | Lind, Thomas Lind, P. Monica Hu, Lijuan Melhus, Håkan |
author_sort | Lind, Thomas |
collection | PubMed |
description | BACKGROUND: The most prominent features of hypervitaminosis A in rats are spontaneous fractures and anorexia. Since caloric restriction induces alterations in bone, some effects could be secondary to loss of appetite. To clarify the mechanisms behind vitamin A-induced bone fragility it is necessary to distinguish between direct and indirect effects. MATERIALS AND METHODS: In this study we compared rats fed high doses of vitamin A both with pair-fed controls, which were fed the same amount of chow as that consumed by the vitamin A group to keep food intake the same, and to controls with free access to food. RESULTS: In contrast to the pair-fed animals, rats in the free access group fed high doses of vitamin A for 7 days had 13% lower food intake, 15% lower body weight, and 2.7% shorter femurs compared with controls. In addition, serum biomarkers of bone turnover were reduced. Peripheral quantitative computed tomography of the femurs showed that the bone mineral content, cross sectional area, and periosteal circumference were similarly reduced in the pair-fed and free access groups. However, bone mineral density (BMD) and cortical parameters were only significantly decreased in the free access group. CONCLUSIONS: Our data indicate that the major direct short-term effect of high doses of vitamin A on rat bone is a reduced bone diameter, whereas the effects on bone length, serum biomarkers of bone turnover, BMD, and bone cortex appear to be mainly indirect, caused by a systemic toxicity with loss of appetite, reduced food intake, and general effects on growth. |
format | Online Article Text |
id | pubmed-6055747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60557472018-07-24 Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding Lind, Thomas Lind, P. Monica Hu, Lijuan Melhus, Håkan Ups J Med Sci Articles BACKGROUND: The most prominent features of hypervitaminosis A in rats are spontaneous fractures and anorexia. Since caloric restriction induces alterations in bone, some effects could be secondary to loss of appetite. To clarify the mechanisms behind vitamin A-induced bone fragility it is necessary to distinguish between direct and indirect effects. MATERIALS AND METHODS: In this study we compared rats fed high doses of vitamin A both with pair-fed controls, which were fed the same amount of chow as that consumed by the vitamin A group to keep food intake the same, and to controls with free access to food. RESULTS: In contrast to the pair-fed animals, rats in the free access group fed high doses of vitamin A for 7 days had 13% lower food intake, 15% lower body weight, and 2.7% shorter femurs compared with controls. In addition, serum biomarkers of bone turnover were reduced. Peripheral quantitative computed tomography of the femurs showed that the bone mineral content, cross sectional area, and periosteal circumference were similarly reduced in the pair-fed and free access groups. However, bone mineral density (BMD) and cortical parameters were only significantly decreased in the free access group. CONCLUSIONS: Our data indicate that the major direct short-term effect of high doses of vitamin A on rat bone is a reduced bone diameter, whereas the effects on bone length, serum biomarkers of bone turnover, BMD, and bone cortex appear to be mainly indirect, caused by a systemic toxicity with loss of appetite, reduced food intake, and general effects on growth. Taylor & Francis 2018-06 2018-06-24 /pmc/articles/PMC6055747/ /pubmed/29697007 http://dx.doi.org/10.1080/03009734.2018.1448020 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ 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 cited. |
spellingShingle | Articles Lind, Thomas Lind, P. Monica Hu, Lijuan Melhus, Håkan Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title | Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title_full | Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title_fullStr | Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title_full_unstemmed | Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title_short | Studies of indirect and direct effects of hypervitaminosis A on rat bone by comparing free access to food and pair-feeding |
title_sort | studies of indirect and direct effects of hypervitaminosis a on rat bone by comparing free access to food and pair-feeding |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055747/ https://www.ncbi.nlm.nih.gov/pubmed/29697007 http://dx.doi.org/10.1080/03009734.2018.1448020 |
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