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雷公藤提取物抑制人滑膜细胞中白细胞介素-1β诱导的环氧化酶-2表达的分子机制。

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

作者信息

Maekawa K, Yoshikawa N, Du J, Nishida S, Kitasato H, Okamoto K, Tanaka H, Mizushima Y, Kawai S

机构信息

Institute of Medical Science, St Marianna University School of Medicine, Miyamae, Kawasaki, Japan.

出版信息

Inflamm Res. 1999 Nov;48(11):575-81. doi: 10.1007/s000110050506.

Abstract

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 ofTWHF (GTW), a TWHF extract, on interleukin (IL)-1beta stimulated human rheumatoid synovial cells.

MATERIALS AND METHODS

IL-1beta-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 E2 production by IL-1beta-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-1beta-induced nuclear factor-kappaB 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 E2 production in human synovial cells due to suppression of COX-2 mRNA, possibly via inhibition of nuclear factor-kappaB activity.

摘要

目的

据报道,雷公藤多苷(TWHF)的几种提取物对类风湿性关节炎患者有效。我们研究了TWHF提取物雷公藤多苷(GTW)对白细胞介素(IL)-1β刺激的人类风湿性滑膜细胞的影响。

材料与方法

在使用各自报告质粒的实验中,用IL-1β刺激的滑膜细胞来检测GTW对环氧合酶(COX)-1和COX-2活性、COX蛋白和mRNA表达以及核转录因子的影响。

结果

GTW以浓度依赖的方式抑制IL-1β刺激的滑膜细胞产生前列腺素E2,并且以与地塞米松相似的方式抑制COX-2蛋白和mRNA表达。然而,GTW并非作为糖皮质激素激动剂起作用。GTW抑制IL-1β诱导的核因子-κB活性,但对激活蛋白-1活性没有显著影响。

结论

GTW或TWHF的抗风湿作用可能部分是通过抑制人滑膜细胞中前列腺素E2的产生介导的,这是由于COX-2 mRNA的抑制,可能是通过抑制核因子-κB活性实现的。

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