Morin inhibits interleukin-1β-induced nitric oxide and prostaglandin E2 production in human chondrocytes

被引:48
作者
Chen, Wei-Ping [1 ]
Wang, Yu-Lu [1 ]
Tang, Jing-Li [1 ]
Hu, Peng-Fei [1 ]
Bao, Jia-Peng [1 ]
Wu, Li-Dong [1 ]
机构
[1] Zhejiang Univ, Dept Orthoped Surg, Coll Med, Affiliated Hosp 2, Hangzhou 310009, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Morin; Nitric oxide; Prostaglandin E2; Inducible NO synthase; Cyclooxygenase; Chondrocyte; NF-KAPPA-B; HUMAN OSTEOARTHRITIC CARTILAGE; GENE-EXPRESSION; ANTIINFLAMMATORY ACTIVITY; ARTICULAR CHONDROCYTES; TNF-ALPHA; INFLAMMATION; CELLS; COX-2; JOINT;
D O I
10.1016/j.intimp.2011.12.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
It is well known that the inflammatory cytokines play important roles in osteoarthritis (OA). In the present study, we investigated the anti-inflammatory properties of morin in chondrocytes. The nitric oxide (NO) production was determined by Griess method, the prostaglandin E2 (PGE(2)) production was detected by Enzyme-linked immunosorbent assay (ELISA). The expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2 were investigated by quantitative real-time PCR and western blot. In addition, western blotting and immunofluorescence staining were performed to investigate the protein level of inhibitor of nuclear factor-kappa B (I kappa B-alpha) and the translocation of nuclear factor kappa B (NF-kappa B). For the in vivo study, morin was administered by intra-articular injection in rats, and the gene expression of iNOS and COX-2 was assessed. We showed that morin inhibited the production of NO and PGE(2) as well as the expression of iNOS and COX-2 in interleukin-l-beta (IL-1 beta)-induced chondrocytes. In addition, morin suppressed the degradation of I kappa B-alpha as well as the translocation of NF-kappa B. In vivo study, morin exerted anti-inflammatory properties in an IL-1 beta-induced rat OA model. Our data suggest that morin possess potential value in the treatment of OA. (C) 2012 Elsevier B.V.. All rights reserved.
引用
收藏
页码:447 / 452
页数:6
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