山竹皮提取物(mpe)和dfdbbx应用于牙槽骨拔牙槽引导骨再生

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引用次数: 0

摘要

目的:研究山竹皮提取物(MPE)和脱矿冻干牛骨异种移植物(DFDBBX)联合应用对牙槽骨成纤维细胞生长因子-2 (FGF-2)表达、成骨细胞数量和破骨细胞数量的临床和微生物学影响。拔牙后牙槽嵴吸收是一个不可避免的生理过程。MPE和DFDBBX的结合有望主要提供骨传导性能,并加强移植物以刺激新骨形成。材料与方法:将56只鱼子狸分为两组,分别进行7 d (A组)和30 d (B组)的检验。每组28只动物接受4种治疗。在每个治疗中,使用7只海茱萸。右下切牙拔除。AI组和BI组牙槽内填充聚乙二醇(PEG) 25 g。AII组和BII组牙槽填充DFDBBX 0.5 g和PEG 24.5 g。AIII组和BIII组牙槽填充0.5 g MPE和24.5 g PEG。AIV组和BIV组牙槽内填充0.5 g DFDBBX、0.5 g MPE和24 g PEG的混合物。分别于第7、30天用乙二胺四乙酸(EDTA)脱钙。在此期间,还进行了组织病理学(HPA)和免疫组织化学(IHC)检测。统计分析:计算成骨细胞数量、破骨细胞数量和FGF-2表达数据采用单因素方差分析。结果:观察7天、30天后,FGF2表达及成骨细胞数量均明显增加。另一方面,破骨细胞数量减少。结论:MPE与DFDBBX联合使用可有效提高海胆牙槽嵴上FGF-2的表达和成骨细胞的数量,减少破骨细胞的数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mangosteen peel extract (mpe) and dfdbbx applied to cavia cobaya tooth extraction sockets for guided bone regeneration
Objectives: The objective of this study was to examine the clinical and microbiological effects of combining mangosteen peel extract (MPE) and demineralized freeze-dried bovine bone xenograft (DFDBBX) on the expression of fibroblast growth factor-2 (FGF-2), the amount of osteoblast, and the amount of osteoclast in the alveolar bone following Cavia cobaya tooth extraction. Tooth extraction followed by alveolar ridge resorption is an unavoidable physiological process. The combination of MPE and DFDBBX is expected to primarily provide osteoconductive properties as well as strengthen the graft in order to stimulate new bone formation. Materials and Methods: Fifty-six Cavia cobaya were divided into two groups for 7-day (group A) and 30-day (group B) examinations, respectively. Each group consisted of twenty-eight animals that received four treatments. In each treatment, seven Cavia cobaya were used. The bottom right incisor was extracted. In groups AI and BI, tooth sockets were filled with 25 grams of polyethylene glycol (PEG). Tooth sockets in groups AII and BII were filled with 0.5 grams of DFDBBX and 24.5 grams of PEG. Tooth sockets in groups AIII and BIII were filled with 0.5 grams of MPE and 24.5 grams of PEG. In groups AIV and BIV, tooth sockets were filled with a mixture of 0.5 grams of DFDBBX, 0.5 grams of MPE, and 24 grams of PEG. Cavia cobaya's mandible was decalcified with ethylene diamine tetraacetic acid (EDTA) at 7 and 30 days. During this time, histopathology (HPA) and immunohistochemistry (IHC) tests were also performed. Statistical analysis: The calculated amounts of osteoblasts, osteoclasts, and FGF-2 expression data were used in the one-way ANOVA test. Results: FGF2 expression and the number of osteoblasts increased significantly after 7-day and 30-day of examination. On the other hand, the number of osteoclasts decreased. Conclusion: The combination of MPE and DFDBBX effectively increases FGF-2 expression and the number of osteoblast cells while decreasing the number of osteoclast cells on the alveolar ridge of Cavia cobaya.
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