Chinese Journal of Tissue Engineering Research ›› 2022, Vol. 26 ›› Issue (14): 2161-2166.doi: 10.12307/2022.477

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Regulatory role of curcumin in hydrogen peroxide-induced autophagy in chondrocytes

Cao Shuxing1, Song Yongzhou1, Li Ming1, Zhang Hongliang1, Zhao Lihui2, Ma Wei1   

  1. 1Department of Orthopedics, Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei Province, China; 2Department of Radiology, Shenze County Hospital, Shenze 052560, Hebei Province, China
  • Received:2021-03-08 Revised:2021-03-09 Accepted:2021-04-28 Online:2022-05-18 Published:2021-12-21
  • Contact: Ma Wei, MD, Chief physician, Department of Orthopedics, Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei Province, China
  • About author:Cao Shuxing, Master, Attending physician, Department of Orthopedics, Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei Province, China
  • Supported by:
    the Scientific Research Fund of Hebei Provincial Health Department, No. 20190068 (to CSX); the Subject of Geriatric Diseases of Hebei Provincial Finance Department, No. 361004 (to LM)

Abstract: BACKGROUND: Curcumin has a good therapeutic effect on osteoarthritis, but the specific mechanism is still unclear. Activation of autophagy can reduce the severity of osteoarthritis. 
OBJECTIVE: To investigate the regulatory effect of curcumin on hydrogen peroxide (H2O2)-induced autophagy in chondrocytes. 
METHODS: C57 mouse articular chondrocytes were cultured in vitro and randomly divided into control group, model group (treated with H2O2) and curcumin low-, medium- and high-dose groups (10, 20, 40, 80 μmol/L). Model group was treated with H2O2 (1 mmol/L) to simulate oxidative stress in osteoarthritis. In the different curcumin groups, chondrocytes were treated with different concentrations of curcumin for 48 hours, followed by addition of H2O2. Twenty-four hours later, the cells were collected for detection. Cell counting kit-8 assay was used to detect cell viability in each group. Interleukin-6 and tumor necrosis factor-α levels were detected by ELISA. TUNEL staining was used to detect cell apoptosis. The apoptosis rate of each group was detected by flow cytometry. The expression levels of cleaved caspase-3, Bax/Bcl2, Beclin1, LC3-II/I, protein kinase B (Akt) and mammalian target of rapamycin (mTOR) were detected by western blot. The expression of cartilage matrix degradation related genes, including matrix metalloproteinase 13, ADAM metallopeptidase with thrombospondin type 1 motif 5, type II collagen α1, and Aggrecan, were detected by qRT-PCR.
RESULTS AND CONCLUSION: Compared with the model group, the activity of chondrocytes was significantly increased after curcumin intervention (P < 0.05). The expression of inflammatory cytokines was significantly decreased (P < 0.05). Apoptosis was significantly decreased (P < 0.05). Apoptosis-related markers, cleaved caspase-3 and Bax/Bcl2 ratio, were significantly decreased (P < 0.05). The expression of autophagy-related markers, LC3-I/II and Beclin1, was significantly increased (P < 0.05). The expression levels of Akt and mTOR were significantly decreased (P < 0.05). qRT-PCR showed that the mRNA expressions of matrix metalloproteinase 13 and ADAM metallopeptidase with thrombospondin type 1 motif 5 were decreased, while the expressions of type II collagen α1 and Aggrecan were increased (P < 0.05). It is suggested that curcumin can reduce the H2O2-induced apoptosis in chondrocytes by promoting autophagy, and this effect may be related to the Akt/mTOR signaling pathway.

Key words: curcumin, osteoarthritis, chondrocyte, autophagy, hydrogen peroxide

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