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ORIGINAL ARTICLE
Year : 2013  |  Volume : 47  |  Issue : 4  |  Page : 395-401

Effects of a selective cyclooxygenase-2 inhibitor (celecoxib) on fracture healing in rats


1 Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China
2 Department of Orthopaedics, Chenzhou People's Hospital, Chenzhou, 423000, Hunan, China

Correspondence Address:
Yong Zhu
Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, 410008, Hunan
China
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Source of Support: This study was supported by the grants from the National 863 project of China (2011AA030101). We also wish to acknowledge that the Celecoxib was provided freely by Pfizer, Conflict of Interest: None


DOI: 10.4103/0019-5413.114930

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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.


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