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Bio-Oss骨复合富血小板纤维蛋白修复兔牙周骨缺损 被引量:2

Repair of rabbit periodontal bone defect with Bio⁃Oss bone combined with platelet⁃rich fibrin
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摘要 目的探讨组织工程骨Bio⁃Oss骨复合富血小板纤维蛋白(PRF)修复牙周骨缺损中骨形成蛋白2(BMP⁃2)、骨保护素(OPG)和核因子κB受体活化因子配体(RANKL)的表达及意义。方法3月龄雄性新西兰大白兔36只,采用随机数表法分为4组,每组9只,制备单侧牙周骨缺损模型,于骨缺损处分别植入Bio⁃Oss骨(Bio⁃Oss组)、PRF(PRF组)和Bio⁃Oss/PRF复合物(Bio⁃Oss/PRF组),以未植入任何材料者作为空白对照。术后4、8和12周处死动物,行大体观察、Masson染色及BMP⁃2、OPG、RANKL免疫组化观察,并对其表达进行析因设计的方差分析。结果Masson染色结果显示,Bio⁃Oss/PRF组术后8周时见部分成熟骨,12周见骨板形成,骨成熟度较高。析因分析显示Bio⁃Oss组在4、8和12周时BMP⁃2表达量逐渐增高,差异有统计学意义(F=51.30,P<0.001);OPG表达量随时间延长先升高后减低,差异有统计学意义(F=167.03,P<0.001);RANKL表达量随时间延长逐渐减低,差异有统计学意义(F=5.39,P=0.046)。PRF组在4、8和12周时BMP⁃2表达量无统计学意义(F=0.68,P=0.544);OPG和RANKL表达量随时间延长逐渐减低,差异有统计学意义(FOPG=1070.93,POPG<0.001;FRANKL=2306.15,PRANKL<0.001)。Bio⁃Oss/PRF组在4、8和12周时BMP⁃2、OPG和RANKL表达量逐渐降低,差异有统计学意义(FBMP⁃2=13.29,PBMP⁃2<0.001;FOPG=237.91,POPG<0.001;FRANKL=132.48,PRANKL<0.001)。空白对照组在4、8和12周时BMP⁃2和OPG表达量先升高后减低,差异有统计学意义(FBMP⁃2=88.33,PBMP⁃2<0.001;FOPG=30.06,POPG<0.001),RANKL表达量随时间推移逐渐减低,差异有统计学意义(F=56.52,P<0.001)。结论Bio⁃Oss骨复合PRF应用可促进成骨以修复牙周骨缺损。 Objective To explore the effect of tissue⁃engineered bone Bio⁃Oss bone combined with platelet⁃rich fibrin(PRF)on repairing periodontal bone defects by examining the expression of bone morphogenetic protein 2(BMP⁃2),osteoprotegerin(OPG)and nuclear factorκB receptor activator ligand(RANKL).Methods A total of 36 three⁃month⁃old male New Zealand white rabbits were divided into four groups by random number table method,i.e.,Bio⁃Oss group,PRF group,Bio⁃Oss/PRF group and blank control group.For each group,there were nine rabbits.Unilateral periodontal was prepared.In the bone defect model,Bio⁃Oss bone,PRF and Bio⁃Oss/PRF composite were implanted in the bone defect,respectively,and the one without any material was used as a blank control.The animals were sacrificed at 4,8 and 12 weeks after the operation.Gross observation,Masson staining and immunohistochemical observation of BMP⁃2,OPG,RANKL were performed,and the expression of the animals was analyzed by factorial design.Results Masson staining results showed that in the Bio⁃Oss/PRF group,some mature bones were observed at 8 weeks after surgery,and bone plates were formed at 12 weeks,with a high bone maturity.Factorial analysis showed that the expression of BMP⁃2 in the Bio⁃Oss group gradually increased at 4,8 and 12 weeks,and the difference was statistically significant(F=51.30,P<0.001);the expression of OPG first rose then descended,and the difference was statistically significant(F=167.03,P<0.001);the expression of RANKL gradually decreased with time,and the difference was statistically significant(F=5.39,P=0.046).The expression of BMP⁃2 in the PRF group at 4,8 and 12 weeks was not statistically significant(F=0.68,P=0.544);the expression of OPG and RANKL decreased gradually over time,and the difference was statistically significant(FOPG=1070.93,POPG<0.001;FRANKL=2306.15,PRANKL<0.001).The expression of BMP⁃2,OPG and RANKL in the Bio⁃Oss/PRF group gradually decreased at 4,8 and 12 weeks,and the difference was statistically significant(FBMP⁃2=13.29,PBMP⁃2<0.001;FOPG=237.91,POPG<0.01;FRANKL=132.48,PRANKL<0.001).In the blank control group,the expression of BMP⁃2 and OPG increased first and then decreased at 4,8 and 12 weeks,and the difference was statistically significant(FBMP⁃2=88.33,PBMP⁃2<0.001;FOPG=30.06,POPG<0.001),while the expression of RANKL gradually decreased over time,and the difference was statistically significant(F=56.52,P<0.001).Conclusion The application of Bio⁃Oss bone composite PRF may promote osteogenesis and repair periodontal bone defects.
作者 张悦 董红宾 张玮 袁媛 周洋 郭涛 Zhang Yue;Dong Hongbin;Zhang Wei;Yuan Yuan;Zhou Yang;Guo Tao(Department of Stomatology,Fifth Affiliated Hospital of Xinjiang Medical University,Urumqi 830000,China;Department of Stomatology,First Affiliated Hospital of Xinjiang Medical University,Urumqi 830054,China)
出处 《中华口腔医学研究杂志(电子版)》 CAS 2020年第5期280-287,共8页 Chinese Journal of Stomatological Research(Electronic Edition)
基金 国家自然科学基金(81660177)。
关键词 富血小板纤维蛋白 骨形成蛋白2 骨保护素 核因子ΚB受体活化因子配体 Bio⁃Oss骨 牙周骨缺损 Platelet⁃rich fibrin Bone morphogenetic protein 2 Osteoprotegerin Receptor activator of nuclear factor kappaB ligand Bio⁃Oss bone Periodontal bone defect
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