Specnuezhenide Decreases Interleukin-1β-Induced Inflammation in Rat Chondrocytes and Reduces Joint Destruction in Osteoarthritic Rats

  • Front Pharmacol. 2018 Jun 28;9:700. doi: 10.3389/fphar.2018.00700.
Chiyuan Ma  1 Xiaopeng Zhou  1 Kai Xu  1 Linyan Wang  2 Yute Yang  1 Wei Wang  1 An Liu  1 Jisheng Ran  1 Shigui Yan  1 Haobo Wu  1 Lidong Wu  1
Affiliations
  • 1. Department of Orthopedics Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • 2. Department of Ophthalmology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Abstract

As a chronic disease, osteoarthritis (OA) leads to the degradation of both cartilage and subchondral bone, its development being mediated by proinflammatory cytokines like interleukin-1β. In the present study, the anti-inflammatory effect of specnuezhenide (SPN) in OA and its underlying mechanism were studied in vitro and in vivo. The results showed that SPN decreases the expression of cartilage matrix-degrading Enzymes and the activation of NF-κB and Wnt/β-catenin signaling, and increases chondrocyte-specific gene expression in IL-1β-induced inflammation in chondrocytes. Furthermore, SPN treatment prevents the degeneration of both cartilage and subchondral bone in a rat model of OA. To the best of our knowledge, this study is the first to report that SPN decreases interleukin-1β-induced inflammation in rat chondrocytes by inhibiting the activation of the NF-κB and Wnt/β-catenin pathways, and, thus, has therapeutic potential in the treatment of OA.

Keywords
NF-κB; chondrocyte; osteoarthritis; specnuezhenide; wnt/β-catenin.
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