Lin Jian-Ping, Shi Zhan-Jun, Shen Ning-Jiang, Wang Jian, Li Zao-Min, Xiao Jun
Department of Orthopedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China; Department of Orthopedic Surgery, Hainan Provincial People's Hospital, Haikou, Hainan 570311, P.R. China.
Department of Orthopedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Exp Ther Med. 2016 Dec;12(6):3595-3601. doi: 10.3892/etm.2016.3839. Epub 2016 Oct 26.
The aim of the present study was to establish an experimental animal model of fracture nonunion, and to investigate the changes in serum biomarker concentrations in fracture nonunion. A total of 20 purebred New Zealand rabbits were divided into two group: A bone defect group and a bone fracture group. In the bone defect group, a 15-mm section of bone (including the periosteum) was removed from the mid-radius, and the medullary cavities were closed with bone wax. In the bone fracture group, the mid-radius was fractured. X-rays were taken and blood samples were collected preoperatively and at 2, 3, 4, 5, 6, 7, 8, 10 and 12 weeks after the surgical procedure. The serum concentrations of osteocalcin (OC) and bone-specific alkaline phosphatase (BSAP) served as markers of bone formation, and those of C-terminal telopeptide of type I collagen (CTX), N-terminal telopeptide of type I collagen (NTX) and tartrate-resistant acid phosphatase 5b (TRACP 5b) served as markers of bone resorption. The concentration levels of the markers were measured using a biotin double-antibody sandwich enzyme-linked immunosorbent assay. In the bone defect group, bone callus was observed on X-ray at 2 weeks in three rabbits and the bone calluses stabilized at 5 weeks; however, none of the bones had healed at 8 weeks. In the bone fracture group, the fracture line was distorted at 2 weeks and bone calluses formed at 6-8 weeks. In the bone defect group, the serum BSAP and TRACP 5b concentrations increased following the surgical procedure, peaked at 4 weeks, began to decrease at 5 weeks and stabilized after 6 weeks. The serum OC concentrations did not change significantly following the surgical procedure. The serum CTX concentrations fluctuated during the first 4 weeks, peaked at 5 weeks, then decreased and stabilized after 6 weeks. The serum NTX concentrations fluctuated during the first 4 weeks, were significantly lower at 5 weeks compared with the other time points and stabilized after 6 weeks. These results suggested that a bone nonunion model can be established in New Zealand rabbits by resecting a 15-mm section of bone from the mid-radius prior to bone wax blocking. Measurement of the serum BSAP, CTX, NTX, and TRACP 5b concentrations may be useful for the early detection of bone nonunion. The serum NTX concentrations changed significantly in rabbits with bone nonunion. Further studies are required in order to determine the feasibility of using serum NTX concentrations for the early diagnosis of bone nonunion.
本研究的目的是建立骨折不愈合的实验动物模型,并研究骨折不愈合时血清生物标志物浓度的变化。总共20只纯种新西兰兔被分为两组:骨缺损组和骨折组。在骨缺损组中,从桡骨中段切除15毫米长的一段骨(包括骨膜),并用骨蜡封闭髓腔。在骨折组中,将桡骨中段骨折。在术前以及手术后2、3、4、5、6、7、8、10和12周拍摄X线片并采集血样。血清骨钙素(OC)和骨特异性碱性磷酸酶(BSAP)的浓度作为骨形成的标志物,而I型胶原C端肽(CTX)、I型胶原N端肽(NTX)和抗酒石酸酸性磷酸酶5b(TRACP 5b)的浓度作为骨吸收的标志物。使用生物素双抗体夹心酶联免疫吸附测定法测量标志物的浓度水平。在骨缺损组中,3只兔子在2周时X线片上观察到骨痂,骨痂在5周时稳定;然而,8周时所有骨头均未愈合。在骨折组中,骨折线在2周时变形,6 - 8周时形成骨痂。在骨缺损组中,血清BSAP和TRACP 5b浓度在手术后升高,在4周时达到峰值,5周时开始下降,6周后稳定。血清OC浓度在手术后无明显变化。血清CTX浓度在最初4周内波动,5周时达到峰值,然后下降并在6周后稳定。血清NTX浓度在最初4周内波动,5周时与其他时间点相比显著降低,6周后稳定。这些结果表明,通过在骨蜡封闭前从桡骨中段切除15毫米长的一段骨,可以在新西兰兔中建立骨折不愈合模型。测量血清BSAP、CTX、NTX和TRACP 5b浓度可能有助于早期检测骨折不愈合。骨折不愈合兔的血清NTX浓度变化显著。需要进一步研究以确定使用血清NTX浓度早期诊断骨折不愈合的可行性。