首页|CGF联合生物骨修复材料修复牙槽缺损对成骨的影响及作用机制分析

CGF联合生物骨修复材料修复牙槽缺损对成骨的影响及作用机制分析

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目的 探讨浓缩生长因子(CGF)联合生物骨修复材料Bio-Oss骨粉修复牙槽缺损对成骨的影响及CT评价.方法 选用8~12月龄的Beagle犬8只(雌雄不限)作为研究对象,每只犬上颌左右对称以人工造裂的方式建立牙槽嵴裂动物模型,分别随机给予动物模型左右侧植入自体骨髂骨松质修复(对照组)、CGF+Bio-Oss混合物修复(实验组),适当加压,充分填匀,保证黏膜瓣无张力的情况下严密缝合.分别于3、6个月通过CT测量计算各组骨吸收率.分别在手术后第3个月处死3只、第6个月处死5只犬,截取犬中切牙远中至尖牙近中侧之间的骨质,进行Micro CT拍摄,测量成骨质量[骨体积分数(BV/TV)、骨小梁厚度(Tb.Th)、骨小梁分离度(Tb.Sp)].按病理学标准制作切片,HE染色,镜下观察并拍照记录.比较两组术后3个月、6个月成骨标记基因、成骨细胞分化基因及成骨细胞凋亡相关基因表达.结果 实验组、对照组术后6个月骨吸收率均大于术后3个月[实验组(18.95±2.27)%比(11.26±1.52)%,对照组(21.99±3.01)%比(15.91±2.36)%](t=5.135、t=2.963,均P<0.05);实验组术后3个月骨吸收率均小于对照组(t=2.869,P<0.05);两组术后6个月骨吸收率比较,差异无统计学意义(t=1.803,P>0.05).实验组、对照组术后6个月BV/TV均大于术后3个月(实验组0.46±0.05比0.39±0.05,对照组0.40±0.04比0.34±0.04),Tb.Sp均小于术后3个月(实验组 0.14±0.02 比 0.18±0.02,对照组 0.17±0.02 比 0.21±0.03)(分别 t=2.215、t=2.304、t=2.311、t=2.237,P<0.05);实验组术后3个月BV/TV大于对照组,Tb.Sp小于对照组(分别t=2.209、t=2.372,P<0.05);术后6个月两组BV/TV、Tb.Sp比较差异无统计学意义(分别t=2.095、t=2.353,P>0.05);术后3个月、6个月两组Tb.Th差异无统计学意义(分别t=2.043、t=2.039,P>0.05).低倍显微镜下观察实验组与对照组的骨组织样本均展现出明显的成熟骨皮质层,这一层紧密地包裹着内部的骨小梁,这些骨小梁以一种杂乱无章方式排列,并被一种富含血液成分的脂肪组织所间隔,这种组织富含红细胞、白细胞等血细胞,并呈现出类似蜂巢的结构;高倍镜下能够更清晰地观察到骨细胞均匀地分布在骨质中,在这些活跃的骨细胞之间,还散布着处于非功能状态的破骨细胞.此外,骨小梁的周围附着有数量相对较少的成骨细胞,这些成骨细胞紧密地贴附在骨小梁表面,而骨小梁之间的空间则由前面提到的富含血细胞的脂肪组织所填充,在这些脂肪组织的交界处,可以观察到血管样的结构,这暗示着骨组织中的血液供应是充足的.术后3个月、6个月,研究组OC、OPG、Runx2 基因表达高于对照组(分别 t=2.526、t=3.046、t=3.660、t=3.941、t=2.933、t=3.145,P<0.05);术后 3个月、6个月,研究组PCNA、ki67基因表达高于对照组,BAX基因表达低于对照组(分别t=8.245、t=8.481、t=10.492、t=8.515、t=5.643、t=6.903,P<0.05).结论 CGF联合生物骨修复材料Bio-Oss骨粉修复牙槽缺损可获得比自体骨移植更好的效果,不仅能有效降低术后骨吸收率,还能促进成骨细胞分化和骨形成,减少成骨细胞异常凋亡.
Effect of CGF combined with biological bone repair materials on osteogenesis of alveolar defect and mecha-nism analysis of CT evaluation
Objective To explore the effect of concentrated growth factor(CGF)combined with Bio-Oss bone powder,a biologic bone repair material,on osteogenesis and CT evaluation of alveolar defect repair.Meth-ods Eight Beagle dogs(male and female)from 8~12 months of age were selected as the study subjects,and each dog was established as an animal model of alveolar crestal fissure by artificial fissure creation in the left and right side of the maxilla symmetrically,and the animal models were randomly given autogenous bone iliac cancellous re-pair(control group)and CGF+Bio-Oss mixture repair(experimental group)on the left and right side,respectively,with appropriate pressure and adequate filling to ensure that the mucosal flap was free of The sutures were tightly closed with no tension.The bone resorption rate was calculated by CT measurement at 3 and 6 months for each group,respectively.The animals were executed at month 6 after surgery,and the bone between the distal middle of the central incisor and the proximal middle of the cuspid was intercepted and fixed in 4%paraformaldehyde for 2 weeks,during which Micro CT was taken to measure the osteogenic quality[bone volume fraction(BV/TV),bone trabecular thickness(Tb.Th),and trabecular separation(Tb.Sp)].Sections were made according to pathological standards,HE stained,microscopically observed and photographed and recorded.The expressions of osteoblast marker genes,osteoblast differentiation genes and osteoblast apoptosis-related genes were compared between the two groups 3 months and 6 months after operation.Results The bone resorption rates of the experimental group and the control group were greater than that of the 3-month postoperative period(experimental group:18.95%±2.27%com-pared to 11.26%±1.52%,control group:21.99%±3.01%compared to 15.91%±2.36%)(t=5.135,2.963,respective-ly,both P<0.05);the bone resorption rates of the experimental group in the 3-month postoperative period were less than that of the control group(t=2.869,P<0.05);the difference in bone resorption rate at 6 months postoperatively between the two groups was not statistically significant(t=1.803,P>0.05).BV/TV was greater in the experimental and control groups at 6 months postoperatively than at 3 months postoperatively(experimental group:0.46±0.05 vs.0.39±0.05,control group:0.40±0.04 vs.0.34±0.04),and Tb.Sp was less than at 3 months postoperatively(experi-mental group:0.14±0.02 vs.0.18±0.02,control group:0.17±0.02 than 0.21±0.03)(t=2.215,2.304,2.311,2.237,respectively,P<0.05);BV/TV was greater than that of the control group in the experimental group at 3 months postoperatively,and Tb.Sp was less than that of the control group(t=2.209,2.372,respectively,P<0.05);and the differences in the BV/TV and Tb.Sp between the two groups at 6 months postoperatively were were not statis-tically significant(t=2.095,2.353,respectively,P>0.05);there was no statistical difference in Tb.Th between the two groups at 3 and 6 months after surgery(t=2.043,2.039,respectively,P>0.05).Under a low magnification mi-croscope,the bone tissue samples from both the experimental and control groups exhibited a distinct layer of mature bone cortex,which was tightly packed with internal bone trabeculae,which were arranged in a haphazard manner and were spaced by an adipose tissue rich in blood constituents,which was enriched with blood cells such as erythro-cytes and leukocytes,and showed a structure similar to a honeycomb.Under high magnification,it was possible to observe more clearly that the osteoblasts were uniformly distributed in the bone,and between these active osteo-blasts,osteoclasts in a non-functional state were scattered.In addition,a relatively small number of osteoblasts were attached around the bone trabeculae,which were tightly adhered to the surface of the trabeculae,whereas the space between the trabeculae was filled by the blood cell-rich adipose tissues mentioned earlier,and vascular-like struc-tures could be observed at the junction of these adipose tissues,which implied that the blood supply to the bone tis-sues was adequate.At 3 and 6 months after surgery,the expressions of OC,OPG and Runx2 genes in the study group were higher than those in the control group(t=2.526,3.046,3.660,3.941,2.933,3.145,respectively,P<0.05).At 3 and 6 months after surgery,PCNA and ki67 gene expressions in the study group were higher than those in the control group,while BAX gene expressions were lower than those in the control group(t=8.245,8.481,10.492,8.515,5.643,6.903,respectively,P<0.05).Conclusion CGF combined with Bio-Oss bone meal can achieve better results than autologous bone transplantation in repairing alveolar defects.It can not only effectively re-duce postoperative bone absorption rate,but also promote osteoblast differentiation and bone formation,and reduce abnormal apoptosis of osteoblasts.

Alveolar defectConcentrated growth factorBio-Oss bone powderRestoration

吕舒颖、焦雪峰、陈金玲、肖高天、阮召伟

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宁德师范学院附属宁德市医院口腔科,福建宁德 352100

牙槽缺损 浓缩生长因子 Bio-Oss骨粉 修复

福建省自然科学基金计划项目

2020J011345

2024

解剖学研究
广东省解剖学会 中国解剖学会

解剖学研究

CSTPCD
影响因子:0.327
ISSN:1671-0770
年,卷(期):2024.46(4)
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