Department of Periodontology, Faculty of Dentistry, Cumhuriyet University, Sivas, Turkey.
Arch Oral Biol. 2012 Nov;57(11):1545-50. doi: 10.1016/j.archoralbio.2012.06.013. Epub 2012 Jul 12.
The aim of this study was to evaluate the effect of alendronate on osseous wound healing in an experimental model.
Critical size defects were created in calvaria of 40 male Wistar rats. The animals were divided into four groups of 10 animals each: autogenous bone graft group; autogenous bone graft with systemic alendronate group (0.01 mg/kg body weight per day for 8 weeks); autogenous bone graft with local alendronate group (1mg/mL for 5 min); non-treatment (control) group. Animals were sacrificed after 8 weeks; osteoblast number, lamellar bone formation, and area of newly formed bone were analysed.
The osteoblast number significantly increased in the autogenous bone graft with local alendronate group compared to the autogenous bone graft group (p<0.05). Both systemic and local application of the alendronate significantly increased the new bone formation compared to the autogenous bone graft group (p<0.05) with no significant difference between local or systemic use (p>0.05). Local alendronate and autogenous bone graft use significantly increased the total bone area compared to autogenous bone graft alone (p<0.05).
Alendronate enhances the new bone formation by autogenous bone graft in the rat calvarial defect model suggesting that the inhibition of the osteoclastic activity allows an increased rate of bone apposition, which could be applicable to the inflammation-induced destruction of the periodontal tissues during disease.
本研究旨在评估阿仑膦酸钠对实验模型中成骨创面愈合的影响。
在 40 只雄性 Wistar 大鼠的颅骨上创建临界尺寸缺陷。将动物分为 4 组,每组 10 只:自体骨移植物组;自体骨移植物加全身阿仑膦酸钠组(每天 0.01mg/kg 体重,持续 8 周);自体骨移植物加局部阿仑膦酸钠组(1mg/mL 作用 5 分钟);未治疗(对照)组。8 周后处死动物;分析成骨细胞数量、板层骨形成和新骨形成面积。
与自体骨移植物组相比,局部应用阿仑膦酸钠的自体骨移植物组成骨细胞数量显著增加(p<0.05)。全身和局部应用阿仑膦酸钠均显著增加了新骨形成,与自体骨移植物组相比(p<0.05),局部或全身应用之间无显著差异(p>0.05)。与单独使用自体骨移植物相比,局部阿仑膦酸钠和自体骨移植物的使用显著增加了总骨面积(p<0.05)。
阿仑膦酸钠增强了大鼠颅骨缺损模型中自体骨移植物的新骨形成,表明抑制破骨细胞活性可增加骨沉积率,这可能适用于疾病过程中牙周组织炎症诱导的破坏。