King G N, Hughes F J
Department of Periodontology, St Bartholomew's and the Royal London School of Medicine and Dentistry, University of London, UK.
J Periodontol. 1999 Oct;70(10):1125-35. doi: 10.1902/jop.1999.70.10.1125.
The purpose of this study was to investigate the influence of occlusal loading on recombinant human bone morphogenetic protein-2 (BMP-2)-induced bone and cementum formation in a previously established rat model of periodontal regeneration during the early and late stages of wound healing.
64 Wistar rats were divided into 8 groups and had surgically created fenestrated defects on the right side of the mandible involving the removal of bone and exposure of the first and second molar roots. Four groups had their right maxillary molars extracted 2 weeks prior to surgery. Ten microl of 100 ug/ml BMP-2 in a collagen membrane was placed in extracted (hypofunctional) and non-extracted (functional) groups (BMPe and BMPf, respectively) while control groups had collagen membrane only (CONe and CONf). Groups were sacrificed at 10 (BMPe, BMPf, CONe, CONf) or 35 days (BMP35e, BMP35f, CON35e, CON35f) postoperatively and tissues processed for histological examination. Transverse 5 microm sections were stained for identification of new bone, ankylosis and cementum formation.
At 10 days, CONe developed greater bone growth compared with CONf (P<0.05), while both BMP groups developed greater bone compared with controls. However, BMPe developed more ankylosis compared with both CONe and CONf while BMPf was significantly greater than CONf only (P<0.05). BMPf only developed significantly greater new cementum compared with controls. At 35 days, BMP35f developed greater bone growth compared with all other groups including BMP35e (P<0.05) and unlike results at 10 days, no differences were apparent between CON35f and CON35e. Unwanted bone growth beyond the defect margin anteriorly was significantly greater in BMP35f.
Results suggest hypofunction stimulates early bone formation. Furthermore, hypofunction and BMP-2 increase the development of transient ankylosis. However, after wound healing is complete, function augments the early effects of BMP-2-induced new bone growth indicating remodeling to physiological levels does not occur. Finally, occlusal loading is both an important stimulus for remodeling and establishment of the periodontal ligament space during early wound healing as well as enhancing BMP-2-induced cementogenesis.
本研究的目的是在先前建立的大鼠牙周再生模型中,研究咬合负荷对重组人骨形态发生蛋白-2(BMP-2)诱导的骨和牙骨质形成在伤口愈合早期和晚期的影响。
64只Wistar大鼠分为8组,在右侧下颌骨手术制造开窗缺损,包括去除骨组织并暴露第一和第二磨牙牙根。四组在手术前2周拔除右上颌磨牙。将10微升含100微克/毫升BMP-2的胶原膜分别置于拔牙组(功能减退组)和未拔牙组(功能正常组)(分别为BMPe和BMPf),而对照组仅放置胶原膜(CONe和CONf)。术后10天(BMPe、BMPf、CONe、CONf)或35天(BMP35e、BMP35f、CON35e、CON35f)处死各组动物,对组织进行处理以进行组织学检查。制作5微米厚的横向切片,染色以鉴定新骨、骨粘连和牙骨质形成。
术后10天,与CONf相比,CONe的骨生长更多(P<0.05),而两个BMP组的骨生长均比对照组更多。然而,与CONe和CONf相比,BMPe的骨粘连更多,而BMPf仅显著大于CONf(P<0.05)。与对照组相比,仅BMPf形成的新牙骨质显著更多。术后35天,与包括BMP35e在内的所有其他组相比,BMP35f的骨生长更多(P<0.05),并且与10天时的结果不同,CON35f和CON35e之间没有明显差异。BMP35f中缺损边缘前方多余的骨生长明显更多。
结果表明功能减退刺激早期骨形成。此外,功能减退和BMP-2增加了短暂性骨粘连的发生。然而,伤口愈合完成后,功能增强了BMP-2诱导的新骨生长的早期效应,表明未发生向生理水平的重塑。最后,咬合负荷既是伤口愈合早期牙周膜间隙重塑和建立的重要刺激因素,也是增强BMP-2诱导的牙骨质生成的因素。