Abstract

Osteoarthritis (OA) is a common degenerative joint disorder that affects joint function, mobility, and pain. The release of proinflammatory cytokines stimulates matrix metalloproteinases (MMPs) and aggrecanase production which further induces articular cartilage degradation. Hypertrophy-like changes in chondrocytes are considered to be an important feature of OA pathogenesis. A Glycyrrhiza new variety, Wongam (WG), was developed by the Korea Rural Development Administration to enhance the cultivation and quality of Glycyrrhizae Radix et Rhizoma (licorice). This study examined the regulatory effect of WG against hypertrophy-like changes such as RUNX2, Collagen X, VEGFA, MMP-13 induction, and Collagen II reduction induced by IL-1β in SW1353 human chondrocytes. Additionally, in silico methods were performed to identify active compounds in licorice to target chondrocyte hypertrophy-related proteins. WG showed inhibitory effects against IL-1β-induced chondrocyte hypertrophy by regulating both HDAC4 activation via the PTH1R/PKA/PP2A pathway and the SOX9/β-catenin signaling pathway. In silico analysis demonstrated that 21 active compounds from licorice have binding potential with 11 targets related to chondrocyte hypertrophy. Further molecular docking analysis and in vivo studies elicited four compounds. Based on HPLC, isoliquiritigenin and its precursors were identified and quantified. Taken together, WG is a potential therapeutic agent for chondrocyte hypertrophy-like changes in OA.

Highlights

  • Osteoarthritis (OA), referred to as degenerative joint disorder, is caused by multiple factors including age, sex, obesity, genetics, joint injury, and diabetes [1]

  • Our results showed that the WG-induced nuclear translocation was decreased by the PKA inhibitor H89 (0.42-fold) and as well as the phosphatase 2A (PP2A) inhibitor okadiac acid (ODA) (0.61-fold) (Figure 3D–F)

  • The potential molecular mechanism involved in the protective effects of WG was HDAC4 activation via the PTH1R/PKA/PP2A pathway

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Summary

Introduction

Osteoarthritis (OA), referred to as degenerative joint disorder, is caused by multiple factors including age, sex, obesity, genetics, joint injury, and diabetes [1]. Hypertrophic chondrocytes, relevant to the terminal differentiation of chondrocytes, express elevated levels of type X collagen (Collagen X), runt-related transcription factor 2 (RUNX2), and MMP13, whereas markers for hyaline cartilage, such as type II collagen (Collagen II) and SRY-related high-mobility group-box gene 9 (SOX9) decrease in OA conditions [8]. Several signaling pathways such as Wnt/β-Catenin, Indian hedgehog (Ihh), parathyroid hormone-related peptide (PTHrP), transforming growth factor-beta (TGF-β), fibroblast growth factor (FGF), SOX9, and bone morphogenetic protein (BMP) signaling are involved in hypertrophy-like changes in chondrocytes [9]

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