骨关节炎
钙黄绿素
氧化应激
活性氧
化学
细胞凋亡
医学
药理学
癌症研究
内分泌学
病理
生物化学
膜
替代医学
作者
Qi He,Junzheng Yang,Zhaofeng Pan,Gangyu Zhang,Bai‐Hao Chen,Shaocong Li,Jiacong Xiao,Fengjin Tan,Zihao Wang,Peng Chen,Haibin Wang
标识
DOI:10.1016/j.biopha.2022.113915
摘要
Iron overload was shown to promote chondrocyte ferroptosis in vivo and in vitro. Moreover, iron overload suppressed the expression of collagen II and induced MMP expression by catalyzing ROS generation with mitochondrial dysfunction. Our results showed that BCA could directly reduce intracellular iron concentration by inhibiting TfR1 and promoting FPN but also target the Nrf2/system xc-/GPX4 signaling pathway to scavenge free radicals and prevent lipid peroxidation. The results of this research indicate that BCA regulates iron homeostasis during the progression of osteoarthritis, which can open a new field of treatment for KOA.
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