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Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats
BACKGROUND: Osteoporosis is one of the world’s major medical burdens in the twenty-first century. Pharmaceutical intervention currently focusses on decelerating bone loss, but phytochemicals such as baicalein, which is a lipoxygenase inhibitor, may rescue bone loss. Studies evaluating the effect of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329162/ https://www.ncbi.nlm.nih.gov/pubmed/30651746 http://dx.doi.org/10.1186/s12986-018-0327-2 |
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author | Saul, Dominik Weber, Marie Zimmermann, Marc Hendrik Kosinsky, Robyn Laura Hoffmann, Daniel Bernd Menger, Björn Taudien, Stefan Lehmann, Wolfgang Komrakova, Marina Sehmisch, Stephan |
author_facet | Saul, Dominik Weber, Marie Zimmermann, Marc Hendrik Kosinsky, Robyn Laura Hoffmann, Daniel Bernd Menger, Björn Taudien, Stefan Lehmann, Wolfgang Komrakova, Marina Sehmisch, Stephan |
author_sort | Saul, Dominik |
collection | PubMed |
description | BACKGROUND: Osteoporosis is one of the world’s major medical burdens in the twenty-first century. Pharmaceutical intervention currently focusses on decelerating bone loss, but phytochemicals such as baicalein, which is a lipoxygenase inhibitor, may rescue bone loss. Studies evaluating the effect of baicalein in vivo are rare. METHODS: We administered baicalein to sixty-one three-month-old female Sprague-Dawley rats. They were divided into five groups, four of which were ovariectomized (OVX) and one non-ovariectomized (NON-OVX). Eight weeks after ovariectomy, bilateral tibial osteotomy with plate osteosynthesis was performed and bone formation quantified. Baicalein was administered subcutaneously using three doses (C1: 1 mg/kg BW; C2: 10 mg/kg BW; and C3: 100 mg/kg BW) eight weeks after ovariectomy for four weeks. Finally, femora and tibiae were collected. Biomechanical tests, micro-CT, ashing, histological and gene expression analyses were performed. RESULTS: Biomechanical properties were unchanged in tibiae and reduced in femora. In tibiae, C1 treatment enhanced callus density and cortical width and decreased callus area. In the C3 group, callus formation was reduced during the first 3 weeks after osteotomy, correlating to a higher mRNA expression of Osteocalcin, Tartrate-resistant acid phosphatase and Rankl. In femora, baicalein treatments did not alter bone parameters. CONCLUSIONS: Baicalein enhanced callus density and cortical width but impaired early callus formation in tibiae. In femora, it diminished the biomechanical properties and calcium-to-phosphate ratio. Thus, it is not advisable to apply baicalein to treat early bone fractures. To determine the exact effects on bone healing, further studies in which baicalein treatments are started at different stages of healing are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12986-018-0327-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6329162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63291622019-01-16 Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats Saul, Dominik Weber, Marie Zimmermann, Marc Hendrik Kosinsky, Robyn Laura Hoffmann, Daniel Bernd Menger, Björn Taudien, Stefan Lehmann, Wolfgang Komrakova, Marina Sehmisch, Stephan Nutr Metab (Lond) Research BACKGROUND: Osteoporosis is one of the world’s major medical burdens in the twenty-first century. Pharmaceutical intervention currently focusses on decelerating bone loss, but phytochemicals such as baicalein, which is a lipoxygenase inhibitor, may rescue bone loss. Studies evaluating the effect of baicalein in vivo are rare. METHODS: We administered baicalein to sixty-one three-month-old female Sprague-Dawley rats. They were divided into five groups, four of which were ovariectomized (OVX) and one non-ovariectomized (NON-OVX). Eight weeks after ovariectomy, bilateral tibial osteotomy with plate osteosynthesis was performed and bone formation quantified. Baicalein was administered subcutaneously using three doses (C1: 1 mg/kg BW; C2: 10 mg/kg BW; and C3: 100 mg/kg BW) eight weeks after ovariectomy for four weeks. Finally, femora and tibiae were collected. Biomechanical tests, micro-CT, ashing, histological and gene expression analyses were performed. RESULTS: Biomechanical properties were unchanged in tibiae and reduced in femora. In tibiae, C1 treatment enhanced callus density and cortical width and decreased callus area. In the C3 group, callus formation was reduced during the first 3 weeks after osteotomy, correlating to a higher mRNA expression of Osteocalcin, Tartrate-resistant acid phosphatase and Rankl. In femora, baicalein treatments did not alter bone parameters. CONCLUSIONS: Baicalein enhanced callus density and cortical width but impaired early callus formation in tibiae. In femora, it diminished the biomechanical properties and calcium-to-phosphate ratio. Thus, it is not advisable to apply baicalein to treat early bone fractures. To determine the exact effects on bone healing, further studies in which baicalein treatments are started at different stages of healing are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12986-018-0327-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-11 /pmc/articles/PMC6329162/ /pubmed/30651746 http://dx.doi.org/10.1186/s12986-018-0327-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Saul, Dominik Weber, Marie Zimmermann, Marc Hendrik Kosinsky, Robyn Laura Hoffmann, Daniel Bernd Menger, Björn Taudien, Stefan Lehmann, Wolfgang Komrakova, Marina Sehmisch, Stephan Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title | Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title_full | Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title_fullStr | Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title_full_unstemmed | Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title_short | Effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
title_sort | effect of the lipoxygenase inhibitor baicalein on bone tissue and bone healing in ovariectomized rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329162/ https://www.ncbi.nlm.nih.gov/pubmed/30651746 http://dx.doi.org/10.1186/s12986-018-0327-2 |
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