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正畸牙齿移动至植骨牙槽裂的生物学效应

Biological Effects of Orthodontic Tooth Movement Into the Grafted Alveolar Cleft.

作者信息

Sun Jian, Zhang Xiaoyue, Li Renmei, Chen Zhengxi, Huang Yuanliang, Chen Zhenqi

机构信息

Resident, Department of Stomatology, Shanghai East Hospital, Tong Ji University School of Medicine, Shanghai, China, and Department of Orthodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Resident, Department of Orthodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

J Oral Maxillofac Surg. 2018 Mar;76(3):605-615. doi: 10.1016/j.joms.2017.08.029. Epub 2017 Aug 24.

Abstract

PURPOSE

Functional stimulus during orthodontic tooth movement into the grafted bone can lead to better alveolar bone grafting outcomes. The aim of this study was to analyze the biological effects of orthodontic tooth movement into the grafted alveolar cleft area with histologic staining, fluorescence staining, and real-time polymerase chain reaction (PCR).

MATERIALS AND METHODS

An animal model of orthodontic tooth movement into the grafted alveolar cleft area was established in 8-week-old Sprague-Dawley rats. The animals were divided into the experimental group and the control group. Four checkpoints were observed: before orthodontic stimuli, day 1 after orthodontic stimuli, day 3 after orthodontic stimuli, and day 5 after orthodontic stimuli. The cleft bone formation conditions, including the collagen fibers and the activities of the osteoclasts and osteoblasts, were evaluated by histologic staining. The expression of tartrate-resistant acid phosphatase (TRAP), receptor activator nuclear factor κB ligand, and Runt-related transcription factor 2 was detected by real-time PCR in both groups.

RESULTS

Hematoxylin-eosin staining showed that the remodeling process of iliac autografts was completed when the orthodontic stress was applied, whereas the bone tissues first showed osteoclastogenesis and then osteogenesis. On the basis of TRAP staining, the osteoclasts increased to the maximal amount on day 3 and decreased thereafter. Evidence from tetracycline fluorescence staining indicated that no obvious changes in osteoblast activity were detected at the early stage; however, it gradually increased, especially in the region close to the root surface. According to real-time PCR, the expression of TRAP increased in both the early and middle stages, that of receptor activator nuclear factor κB ligand increased in the early stage, and that of Runt-related transcription factor 2 increased in the late stage. Moreover, the results showed significant differences between the experimental and control groups.

CONCLUSIONS

Orthodontic tooth movement into the alveolar cleft bone graft area promoted bone remodeling of embedded bone, thus inducing bone resorption and subsequent deposition.

摘要

目的

正畸牙齿移动至移植骨区域过程中的功能性刺激可带来更好的牙槽骨移植效果。本研究旨在通过组织学染色、荧光染色及实时聚合酶链反应(PCR)分析正畸牙齿移动至移植牙槽裂区域的生物学效应。

材料与方法

在8周龄的斯普拉格-道利大鼠中建立正畸牙齿移动至移植牙槽裂区域的动物模型。将动物分为实验组和对照组。观察四个时间点:正畸刺激前、正畸刺激后第1天、正畸刺激后第3天和正畸刺激后第5天。通过组织学染色评估裂隙骨形成情况,包括胶原纤维以及破骨细胞和成骨细胞的活性。两组均通过实时PCR检测抗酒石酸酸性磷酸酶(TRAP)、核因子κB受体活化因子配体及 runt相关转录因子2的表达。

结果

苏木精-伊红染色显示,施加正畸力时髂骨自体移植骨的重塑过程已完成,而骨组织先是出现破骨细胞生成,随后出现成骨。基于TRAP染色,破骨细胞在第3天增加至最大数量,此后减少。四环素荧光染色结果表明,早期未检测到成骨细胞活性有明显变化;然而,其逐渐增加,尤其是在靠近牙根表面的区域。根据实时PCR结果,TRAP的表达在早期和中期均增加,核因子κB受体活化因子配体的表达在早期增加,runt相关转录因子2的表达在后期增加。此外,结果显示实验组和对照组之间存在显著差异。

结论

正畸牙齿移动至牙槽裂骨移植区域可促进植入骨的骨重塑,从而诱导骨吸收及随后的骨沉积。

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