The molecular mechanism of inhibition of interleukin-1β-induced cyclooxygenase-2 expression in human synovial cells by Tripterygium wilfordii Hook F extract

被引:32
作者
Maekawa, K
Yoshikawa, N
Du, J
Nishida, S
Kitasato, H
Okamoto, K
Tanaka, H
Mizushima, Y
Kawai, S
机构
[1] St Marianna Univ, Sch Med, Inst Med Sci, Kawasaki, Kanagawa 2168512, Japan
[2] Asahikawa Med Coll, Dept Internal Med 2, Asahikawa, Hokkaido 0788510, Japan
关键词
Tripterygium wilfordii Hook F; cyclooxygenase-2; glucocorticoid receptor; nuclear factor-kappa B; synovial cells;
D O I
10.1007/s000110050506
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Several extracts of Tripterygium wilfordii Hook F (TWHF) have been reported to be effective in patients with rheumatoid arthritis. We investigated the effect of multi-glycosides of TWHF (GTW), a TWHF extract, on interleukin (TL)-1 beta-stimulated human rheumatoid synovial cells. Materials and Methods. IL-1 beta-stimulated synovial cells were used to detect the effects of GTW on cyclooxygenase (COX)-1 and COX-2 activities, expression of COX protein and mRNA, and nuclear transcription factors in experiments using respective reporter plasmids. Results: GTW inhibited prostaglandin E-2 production by IL-1 beta-stimulated synovial cells in a concentration-dependent manner, and also inhibited COX-2 protein and mRNA expression in a similar fashion to dexamethasone. However, GTW did not act as a glucocorticoid agonist. GTW repressed IL-1 beta-induced nuclear factor-kappa B activity, but did not have a significant influence on activating protein-1 activity. Conclusion: The anti-rheumatic effect of GTW or TWHF may be partly mediated through the inhibition of prostaglandin E-2 production in human synovial cells due to suppression of COX-2 mRNA, possibly via inhibition of nuclear factor-kappa B activity.
引用
收藏
页码:575 / 581
页数:7
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