4.6 Article

The effect of resveratrol on normal and osteoarthritic chondrocyte metabolism

期刊

BONE & JOINT RESEARCH
卷 3, 期 3, 页码 51-59

出版社

BRITISH EDITORIAL SOC BONE JOINT SURGERY
DOI: 10.1302/2046-3758.33.2000226

关键词

Resveratrol; SIRT1; Osteoarthritis; Chondrocyte; Longevity; Metabolism

资金

  1. Department of Orthopaedic Surgery

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Background Resveratrol is a polyphenolic compound commonly found in the skins of red grapes. Sirtuin 1 (SIRT1) is a human gene that is activated by resveratrol and has been shown to promote longevity and boost mitochondrial metabolism. We examined the effect of resveratrol on normal and osteoarthritic (OA) human chondrocytes. Methods Normal and OA chondrocytes were incubated with various concentrations of resveratrol (1 mu M, 10 mu M, 25 mu M and 50 mu M) and cultured for 24, 48 or 72 hours or for six weeks. Cell proliferation, gene expression, and senescence were evaluated. Results SIRT1 was significantly upregulated in normal chondrocytes with resveratrol concentrations of 25 mu M and 50 mu M on both two- (2D) (both p = 0.001) and three-dimensional (3D) cultures (p = 0.008 and 0.001, respectively). It was significantly upregulated in OA chondrocytes treated with 10 mu M, 25 mu M and 50 mu M resveratrol on 2D cultures (p = 0.036, 0.002 and 0.001, respectively) and at 50 mu M concentration on 3D cultures (p = 0.001). At 72 hours, the expression of collagen (COL)-10, aggrecan (AGG), and runt-related transcription factor 2 (RUNX2) was significantly greater in both 25 mu M (p = 0.011, 0.006 and 0.015, respectively) and 50 mu M (p = 0.019, 0.004 and 0.002, respectively) resveratrol-treated normal chondrocyte cultures. In OA chondrocytes, expression of COL10 and RUNX2 was significantly greater in 25 mu M (p = 0.004 and 0.024) and 50 mu M (p = 0.004 and 0.019) cultures at 72 hours on 3D cultures. Conclusions At concentrations of 25 mu M and/or 50 mu M, resveratrol treatment significantly upregulates SIRT1 gene expression in normal and osteoarthritic chondrocytes. Resveratrol induces chondrocytes into a hypertrophic state through upregulation of COL1, COL10, and RUNX2.

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