Int J Oral Maxillofac Implants. 2020 Jan/Feb;35(1):70-78. doi: 10.11607/jomi.7745.
The purpose of this study was to evaluate bone repair with two bone substitutes, deproteinized bovine bone and biphasic calcium phosphate ceramics, associated with autogenous bone.
The experimental groups were as follows: autogenous bone only (AB), autogenous bone/deproteinized bovine bone (1:1), and autogenous bone/biphasic calcium phosphate ceramic (1:1). After 30, 60, and 90 days, animals were euthanized and samples were collected for microcomputed tomography (micro-CT), histologic, histomorphometric, and expression analyses of VEGFA, RUNX2, ALP, COL1A1, OCN, PHEX, RANKL, and OPG genes by real-time polymerase chain reaction (PCR) array.
Histomorphometric analysis showed no difference in the amount of immature bone between AB and AB/biphasic calcium phosphate ceramic at 30 and 60 days. There was less mature bone formation in the AB/deproteinized bovine bone at 60 days compared with AB/biphasic calcium phosphate ceramic and AB, and a lower amount of immature bone in the AB/deproteinized bovine bone at 30 and 60 days compared with the AB (P ≤ .05). Micro-CT analysis showed higher immature bone volume (BVI) in the AB/biphasic calcium phosphate ceramic at 60 days and lower BVI at 90 days (P ≤ .05). Molecular analysis showed a lower expression of all genes in the AB/deproteinized bovine bone and AB/biphasic calcium phosphate ceramic compared with AB at all time points. A greater expression of RANKL was found in the AB/deproteinized bovine bone compared with AB/biphasic calcium phosphate ceramic at 30 days (P ≤ .05), and a lower expression of the OC, RUNX2, and ALP genes in AB/deproteinized bovine bone and AB/biphasic calcium phosphate ceramic was found compared with AB at all time points (P ≤ .05).
The use of biphasic calcium phosphate ceramic resulted in greater immature bone formation than deproteinized bovine bone at an early assessment. The studied bone regeneration genes were downregulated in comparison to the control.
本研究旨在评估两种骨替代物(脱蛋白牛骨和双相磷酸钙陶瓷)与自体骨联合应用的骨修复效果。
实验组如下:自体骨(AB)、自体骨/脱蛋白牛骨(1:1)和自体骨/双相磷酸钙陶瓷(1:1)。30、60 和 90 天后,处死动物并采集样本,进行微计算机断层扫描(micro-CT)、组织学、组织形态计量学以及血管内皮生长因子 A(VEGFA)、核心结合因子 α1(RUNX2)、碱性磷酸酶(ALP)、Ⅰ型胶原(COL1A1)、骨钙素(OCN)、肽酶 X(PHEX)、核因子 κB 受体活化因子配体(RANKL)和骨保护素(OPG)基因的实时聚合酶链反应(PCR)分析。
组织形态计量学分析显示,30 和 60 天时,AB 与 AB/双相磷酸钙陶瓷之间未成熟骨量无差异。60 天时,AB/脱蛋白牛骨中的成熟骨形成较少,与 AB/双相磷酸钙陶瓷和 AB 相比,AB/脱蛋白牛骨中的未成熟骨较少(P≤0.05)。micro-CT 分析显示,60 天时 AB/双相磷酸钙陶瓷中的未成熟骨体积(BVI)较高,90 天时 BVI 较低(P≤0.05)。分子分析显示,在所有时间点,AB/脱蛋白牛骨和 AB/双相磷酸钙陶瓷中的所有基因表达均低于 AB。30 天时,AB/脱蛋白牛骨中 RANKL 的表达高于 AB/双相磷酸钙陶瓷(P≤0.05),AB/脱蛋白牛骨和 AB/双相磷酸钙陶瓷中 OC、RUNX2 和 ALP 基因的表达均低于 AB(P≤0.05)。
在早期评估中,双相磷酸钙陶瓷的应用导致未成熟骨形成多于脱蛋白牛骨。与对照组相比,研究中的骨再生基因表达下调。