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槲皮素,一种生物类黄酮,可抑制肿瘤坏死因子-α在培养的人滑膜细胞中诱导白细胞介素8和单核细胞趋化蛋白-1表达。

Quercetin, a bioflavonoid, inhibits the induction of interleukin 8 and monocyte chemoattractant protein-1 expression by tumor necrosis factor-alpha in cultured human synovial cells.

作者信息

Sato M, Miyazaki T, Kambe F, Maeda K, Seo H

机构信息

Department of Endocrinology and Metabolism, Nagoya University, Japan.

出版信息

J Rheumatol. 1997 Sep;24(9):1680-4.

PMID:9292787
Abstract

OBJECTIVE

Tumor necrosis factor (TNF)-alpha is present in synovial fluid of patients with rheumatoid arthritis. It induces the expression of proinflammatory cytokines in synovial cells. Based on our recent finding that reactive oxygen intermediates play important roles in mediating TNF-alpha action, we examined the effect of an antioxidant bioflavonoid, quercetin, on TNF-alpha induced expression of interleukin 8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) in cultured human synovial cells.

METHODS

The amounts of mRNA for IL-8 and MCP-1 were determined by Northern blot analysis. Electrophoretic mobility shift assays (EMSA) were performed for the detection of a transcription factor, nuclear factor-kappa B (NF-kappa B).

RESULTS

Addition of quercetin suppressed TNF-alpha induced increase in the mRNA for IL-8 and MCP-1 in a dose dependent manner. Quercetin did not affect the stability of these mRNA. H2O2 mediated induction of IL-8 and MCP-1 genes was also inhibited by quercetin. EMSA revealed that quercetin inhibited the activation of NF-kappa B by TNF-alpha.

CONCLUSION

Quercetin suppresses TNF-alpha mediated stimulation of IL-8 and MCP-1 expression, at least in part, by inhibiting the activation of NF-kappa B.

摘要

目的

肿瘤坏死因子(TNF)-α存在于类风湿性关节炎患者的滑液中。它可诱导滑膜细胞中促炎细胞因子的表达。基于我们最近发现活性氧中间体在介导TNF-α作用中起重要作用,我们研究了抗氧化生物类黄酮槲皮素对TNF-α诱导培养的人滑膜细胞中白细胞介素8(IL-8)和单核细胞趋化蛋白-1(MCP-1)表达的影响。

方法

通过Northern印迹分析确定IL-8和MCP-1的mRNA量。进行电泳迁移率变动分析(EMSA)以检测转录因子核因子-κB(NF-κB)。

结果

添加槲皮素以剂量依赖性方式抑制TNF-α诱导的IL-8和MCP-1 mRNA增加。槲皮素不影响这些mRNA的稳定性。槲皮素也抑制H2O2介导的IL-8和MCP-1基因诱导。EMSA显示槲皮素抑制TNF-α对NF-κB的激活。

结论

槲皮素至少部分地通过抑制NF-κB的激活来抑制TNF-α介导的IL-8和MCP-1表达的刺激。

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