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选择性环氧化酶-2抑制剂(塞来昔布)对大鼠骨折愈合的影响。

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

作者信息

Li Kang-Hua, Cheng Liang, Zhu Yong, Deng Guo-Bing, Long Hai-Tao

机构信息

Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Indian J Orthop. 2013 Jul;47(4):395-401. doi: 10.4103/0019-5413.114930.

Abstract

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.

摘要

背景

多项研究表明塞来昔布会干扰骨愈合,而其他研究则与这些结果相矛盾。本研究旨在基于体表面积换算剂量,探讨塞来昔布对大鼠股骨模型骨愈合的影响。

材料与方法

72只成年雌性Sprague Dawley大鼠在右侧股骨中段无移位横行骨干骨折内固定术后随机分为三组。每组分别在术后用1%甲基纤维素、塞来昔布(21毫克/千克/天)治疗1周或塞来昔布(21毫克/千克/天)治疗4周。术后3、4、6周通过X线片评估骨愈合评分和骨痂形成情况。其中一半大鼠在术后4周处死进行组织学分析。其余骨折股骨在术后6周进行生物力学测试评估。

结果

术后3、4、6周,短期和长期组骨折愈合的平均X线评分均低于对照组,三组间差异有统计学意义(P<0.05)。两组的平均骨小梁密度均小于对照组,在4周时差异也有统计学意义(P<0.05)。术后6周,短期和长期组的最大负荷、总能量和刚度与对照组相比均显著降低(P<0.05)。

结论

在大鼠模型中,短期和长期持续使用塞来昔布对大鼠骨折愈合均有显著抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a5e/3745695/0ff9d0fed7c1/IJOrtho-47-395-g002.jpg

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