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Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats
BACKGROUND: Several studies suggested that celecoxib interferes with bone healing while others contradict these findings. This study was conducted to investigate the effects of celecoxib on bone healing in rats femur mold with a dose based on body surface area conversion. MATERIALS AND METHODS: 72 a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745695/ https://www.ncbi.nlm.nih.gov/pubmed/23960285 http://dx.doi.org/10.4103/0019-5413.114930 |
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author | Li, Kang-Hua Cheng, Liang Zhu, Yong Deng, Guo-Bing Long, Hai-Tao |
author_facet | Li, Kang-Hua Cheng, Liang Zhu, Yong Deng, Guo-Bing Long, Hai-Tao |
author_sort | Li, Kang-Hua |
collection | PubMed |
description | BACKGROUND: Several studies suggested that celecoxib interferes with bone healing while others contradict these findings. This study was conducted to investigate the effects of celecoxib on bone healing in rats femur mold with a dose based on body surface area conversion. MATERIALS AND METHODS: 72 adult female Sprague Dawley rats were randomly divided into three groups after the internal fixation operation of nondisplaced transverse mid diaphyseal fractures of the right femurs. Each group was treated with 1% methylcellulose, celecoxib (21 mg/kg/d) for 1 week, or celecoxib (21 mg/kg/d) for 4 weeks after surgeries respectively. Bone healing scores and callus formation were evaluated by radiographs at 3, 4, 6 weeks after surgeries. Half of these rats were sacrificed for histological analysis at 4 weeks after surgery. The remaining fractured femurs were evaluated by biomechanical tests at 6 weeks after surgery. RESULTS: The mean radiographic scores for fracture healing of both short and long term groups were lower than that of the control group and the differences among the three groups were statistically significant (P < 0.05) at 3, 4, 6 weeks after surgery. The mean bone trabecula density of both groups was smaller than that of the control group and the differences were also statistically significant (P < 0.05) at 4 week. The maximum load, total energy and stiffness in both the short term and long term groups were significantly decreased compared with those in the control group (P < 0.05) at 6 week. CONCLUSION: Both short term and long term sustained use of celecoxib in rat models has significantly inhibitory effects on rat fracture healing. |
format | Online Article Text |
id | pubmed-3745695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37456952013-08-19 Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats Li, Kang-Hua Cheng, Liang Zhu, Yong Deng, Guo-Bing Long, Hai-Tao Indian J Orthop Original Article BACKGROUND: Several studies suggested that celecoxib interferes with bone healing while others contradict these findings. This study was conducted to investigate the effects of celecoxib on bone healing in rats femur mold with a dose based on body surface area conversion. MATERIALS AND METHODS: 72 adult female Sprague Dawley rats were randomly divided into three groups after the internal fixation operation of nondisplaced transverse mid diaphyseal fractures of the right femurs. Each group was treated with 1% methylcellulose, celecoxib (21 mg/kg/d) for 1 week, or celecoxib (21 mg/kg/d) for 4 weeks after surgeries respectively. Bone healing scores and callus formation were evaluated by radiographs at 3, 4, 6 weeks after surgeries. Half of these rats were sacrificed for histological analysis at 4 weeks after surgery. The remaining fractured femurs were evaluated by biomechanical tests at 6 weeks after surgery. RESULTS: The mean radiographic scores for fracture healing of both short and long term groups were lower than that of the control group and the differences among the three groups were statistically significant (P < 0.05) at 3, 4, 6 weeks after surgery. The mean bone trabecula density of both groups was smaller than that of the control group and the differences were also statistically significant (P < 0.05) at 4 week. The maximum load, total energy and stiffness in both the short term and long term groups were significantly decreased compared with those in the control group (P < 0.05) at 6 week. CONCLUSION: Both short term and long term sustained use of celecoxib in rat models has significantly inhibitory effects on rat fracture healing. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3745695/ /pubmed/23960285 http://dx.doi.org/10.4103/0019-5413.114930 Text en Copyright: © Indian Journal of Orthopaedics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Li, Kang-Hua Cheng, Liang Zhu, Yong Deng, Guo-Bing Long, Hai-Tao Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title | Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title_full | Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title_fullStr | Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title_full_unstemmed | Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title_short | Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
title_sort | effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745695/ https://www.ncbi.nlm.nih.gov/pubmed/23960285 http://dx.doi.org/10.4103/0019-5413.114930 |
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