| Literature DB >> 32222871 |
Wenhan Wang1,2, Ruitong Yang1,2, Minfa Zhang3, Jiayi Li2, Jiangfan Peng2, Mingyang Xu2, Yunpeng Zhao1, Hao Li4, Xin Pan5.
Abstract
Osteoarthritis (OA), a chronic joint disease, is characterized by cartilage surface erosion, subchondral bone rebuilding, and formation of osteophytes. To date, the nosogenesis and underlying mechanisms of OA have not yet been elucidated. However, it is widely accepted that TNF-α is a crucial cytokine in the development of OA. Glycitin, a natural isoflavone extracted from legumes, affects physiological reactions and pathological responses. Recently, the anti-inflammatory effect of glycitin has been reported. However, the function of glycitin in cartilage degeneration in OA remains to be investigated. In the current study, primary murine chondrocytes were isolated and stimulated by TNF-α to evaluate the anti-inflammatory effects and protective function of glycitin in chondrocytes. In vivo, the ACLT mouse model, a frequently-used OA model, was used to further examine the therapeutic role of glycitin in cartilage degeneration and inflammation in OA. Consequently, glycitin functions were examined both in vivo and in vitro. Moreover, the underlying mechanism of action of glycitin was investigated and was found to involve the NF-κB signaling pathway. Collectively, this study suggests that glycitin can be potentially used for the treatment of joint degenerative diseases, including OA.Entities:
Keywords: NF-κB signaling pathway; glycitin; inflammation; osteoarthritis
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Year: 2020 PMID: 32222871 DOI: 10.1007/s10753-020-01210-3
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.657