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木犀草素对骨缺损成骨修复的作用及机制研究 被引量:6
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作者 汤胜尧 胡珉华 +4 位作者 周若愚 孙伟鹏 唐鑫陶 林海雄 姜自伟 《中国药房》 CAS 北大核心 2023年第7期807-813,共7页
目的探讨木犀草素对骨缺损成骨修复的作用及机制。方法通过网络药理学方法筛选木犀草素治疗骨缺损的作用靶点及潜在通路,利用Hub基因筛选排名前2位的靶点进行分子对接验证,以结合能作为评判标准。对大鼠骨髓间充质干细胞(BMSC)及脐静脉... 目的探讨木犀草素对骨缺损成骨修复的作用及机制。方法通过网络药理学方法筛选木犀草素治疗骨缺损的作用靶点及潜在通路,利用Hub基因筛选排名前2位的靶点进行分子对接验证,以结合能作为评判标准。对大鼠骨髓间充质干细胞(BMSC)及脐静脉内皮细胞(RUVEC)进行体外实验,采用碱性磷酸酶染色、茜素红S染色、体外血管形成实验进行表型验证,采用Western blot法检测磷脂酰肌醇3激酶(PI3K)、蛋白激酶B1(Akt1)蛋白的表达情况,以验证木犀草素对BMSC成骨分化及RUVEC体外血管形成的作用机制。结果网络药理学结果显示,木犀草素对骨缺损的血管形成和骨修复作用主要与Akt1、SRC蛋白、雌激素受体1、表皮生长因子受体、环加氧酶2、基质金属蛋白酶9靶点有关,且与PI3K/Akt信号通路关系密切。分子对接结果显示,木犀草素与Akt1、SRC蛋白结合稳定。体外实验结果表明,木犀草素能显著增高BMSC内碱性磷酸酶的表达水平和活性,增加钙盐沉积和钙化结节的数量,促进BMSC的钙化;与木犀草素0μmol/L组比较,木犀草素1、10μmol/L组的RUVEC血管形成能力显著增强、血管长度显著增加,PI3K、Akt1的蛋白表达水平显著提高(P<0.05或P<0.01),且浓度越高效果越好。结论木犀草素可能通过激活PI3K/Akt信号通路,促进PI3K、Akt1蛋白的表达来发挥增强骨折端的血管形成及骨修复的功能。 展开更多
关键词 木犀草素 缺损 成骨修复 血管形 网络药理学 分子对接
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Osteogenic capability of autologous rabbit adipose-derived stromal cells in repairing calvarial defects 被引量:2
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作者 CHENG Shao-wen LIN Zhong-qin +8 位作者 WANG Wei ZHANG Wei KOU Dong-quan YING Xiao-zhou CHEN Qing-yu SHEN Yue CHENG Xiao-jie PENG Lei LU Chuan-zhu 《Chinese Journal of Traumatology》 CAS 2011年第5期288-292,共5页
Objective: To evaluate the in vitro and in vivo osteogenic capability of adipose-derived stromal cells (ASCs).Methods: ASCs were isolated from New Zealand white rabbits and determined by alkaline phosphatase (ALP... Objective: To evaluate the in vitro and in vivo osteogenic capability of adipose-derived stromal cells (ASCs).Methods: ASCs were isolated from New Zealand white rabbits and determined by alkaline phosphatase (ALP)staining, von Kossa staining and alizarin red staining. Some specific markers ofosteogenic differentiation, including ALP,osteocalcin (OCN), osteopontin (OPN) were examined by reverse transcription-polymerase chain reaction (RT-PCR).In vivo, demineralized bone matrix (DBM)-ASCs composites were implanted into the rabbit calvarial defects created at each side of the longitudinal midline. After 6 weeks, histologic properties of the transplants were analyzed.Results: ASCs were successfully induced into osteogenesis. ALP staining, von Kossa staining and alizarin red staining showed positive results. The expressions of ALP, OCN and OPN were detected in ASCs after cultivation in osteogenic medium. Extensive new bone was observed in the defects transplanted with DBM-ASCs composites.Conclusion: ASCs have the potential to differentiate into osteogenic lineage and DBM-ASCs constructs are a promising method for regeneration in bone defects. 展开更多
关键词 Adipose tissue Bone regeneration OSTEOGENESIS
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