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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...

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Autores principales: Saul, Dominik, Weber, Marie, Zimmermann, Marc Hendrik, Kosinsky, Robyn Laura, Hoffmann, Daniel Bernd, Menger, Björn, Taudien, Stefan, Lehmann, Wolfgang, Komrakova, Marina, Sehmisch, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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