Celecoxib inhibits the heterotopic ossification in the rat model with Achilles tenotomy

被引:20
|
作者
Zhang K. [1 ,3 ]
Wang L. [3 ]
Zhang S. [1 ]
Yu B. [1 ]
Liu F. [2 ]
Cui Z. [1 ]
Jin D. [3 ]
Bai X. [4 ]
机构
[1] Department of Orthopedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515
[2] Department of Cardiology, Nanfang Hospital, Southern Medical University
[3] Department of Orthopedic, Third Affiliated Hospital of Southern Medical University
[4] Department of Cell Biology, School of Basic Medical Sciences, Southern Medical University
关键词
Achilles tenotomy; Celecoxib; COX-2; Heterotopic ossification; Prostaglandins;
D O I
10.1007/s00590-012-0944-9
中图分类号
学科分类号
摘要
Celecoxib, a selective cox-2 inhibitor, has been shown to prevent the heterotopic ossification following total hip arthroplasty. However, the effects of celecoxib on heterotopic ossification at other locations remain unclear. This study aimed to investigate the effect of celecoxib on heterotopic ossification in the rat model with Achilles tenotomy. Forty male Sprague-Dawley rats, which were randomly divided into 2 groups (n = 20), underwent midpoint Achilles tenotomy on left legs through a posterior approach under aseptic condition. Experimental group was treated with the saline solution of celecoxib (10 mg/kg) per day, while control group was treated by normal saline (0.9%). At 3, 5 and 10 postoperative weeks, all animals were examined by X-ray to assess new bone formation in the Achilles tendon. At 10 weeks after surgery, all animals were killed and Achilles tendons were taken for hematoxylin-eosin (HE) and immunohistochemical staining. Heterotopic ossification developed in 3 rats (15%) in experimental group and 20 rats (100%) in control group by postoperative 10 weeks. The incidence of heterotopic ossification was significantly lower in experimental group than in control group (P < 0.05). Our findings suggest that celecoxib inhibits HO development in rat model with Achilles tenotomy. © 2012 Springer-Verlag.
引用
收藏
页码:145 / 148
页数:3
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