体内
免疫印迹
骨关节炎
体外
基质金属蛋白酶
化学
软骨
αBκ
药理学
肿瘤坏死因子α
NF-κB
分子生物学
免疫学
细胞凋亡
医学
病理
生物化学
生物
解剖
基因
生物技术
替代医学
作者
Xu Chen,Mengfei Wang,Hui Li,Xing Yuwen,Xiaochan He,You‐Zeng Hao,Chao Lu
标识
DOI:10.1016/j.imlet.2023.04.007
摘要
Osteoarthritis (OA) is a degenerative joint disease characterized by the destruction of articular cartilage. Tenacissoside G is a flavonoid isolated from the dry roots of Marsdenia tenacissima (Roxb) and has been shown to have anti-inflammatory effects. However, there is no report on the protective effects of Tenacissoside G on OA.To identify the effects and mechanism of Tenacissoside G on OA.In vitro, primary mouse chondrocytes were induced with IL-1β to establish OA model. mRNA expression of MMP-13, MMP-3, TNF-α, IL-6 and iNOS, was detected by PCR. Protein expression of Collagen-II, MMP-13, p65, p-p65, and IκBα was detected by Western blot. Collagen-II in chondrocytes was also detected by immunofluorescence. In vivo, we established DMM OA mice model. The preventive effect of Tenacissoside G on OA was observed by micro-CT and histological analysis.In vitro, Tenacissoside G significantly inhibited the expression of iNOS, TNF-α, IL-6, MMP-3, MMP-13 and the degradation of collagen-II, Tenacissoside G also significantly suppressed NF-κB activation in chondrocytes by IL-1β-stimulated. In vivo, we demonstrated Tenacissoside G can decrease articular cartilage damage and reduce OARSI score.These results suggest that Tenacissoside G may serve as a potential drug for the prevention and treatment of OA.
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