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首页> 外文期刊>International immunopharmacology >Caffeic acid alleviates inflammatory response in rheumatoid arthritis fibroblast-like synoviocytes by inhibiting phosphorylation of I kappa B kinase alpha/beta and I kappa B alpha
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Caffeic acid alleviates inflammatory response in rheumatoid arthritis fibroblast-like synoviocytes by inhibiting phosphorylation of I kappa B kinase alpha/beta and I kappa B alpha

机译:通过抑制IκB激酶α/β和IκBα的磷酸化,通过抑制磷酸化,咖啡酸可减轻类风湿性关节炎成纤维细胞样Synociocytes的炎症反应

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摘要

Caffeic acid (CA) is a phenolic acid widely found in fruits and plants, which exhibits anti-oxidative, anti-inflammatory, anti-tumor and immunomodulatory properties. Because increased level of reactive oxygen species (ROS) is related to the pathogenesis of rheumatoid arthritis (RA), we treated RA-derived fibroblast-like synoviocytes (RA-FLS) with CA, and investigated its effects on cytokine production, expression levels of prostaglandin E2 (PGE2) and matrix metalloproteinases (MMP)-1. Our results showed that high level of CA induced cell apoptosis in RA-FLS. CA significantly reduced productions of interleukin (IL)-6 and tumor necrosis factor-alpha (TNF-alpha) in FLS. Moreover, PGE2 and MMP-1, which play vital roles in RA development, were significantly repressed by CA at both transcriptional and translational levels. To reveal the underlying mechanisms, we compared the levels of proteins involved in mitogen-activated protein kinase (MAPK) and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) signaling pathways between CA and vehicle treated groups, and found that CA exerted its regulatory function on cytokine production via inhibiting phosphorylation of NF-kappa B inhibitor kinase (I kappa B kinase/IKK) alpha/beta and I kappa B alpha. In conclusion, this study has, for the first time, demonstrated the effects of CA on repressing IL-6 and TNF-alpha to alleviate inflammation response in RA-FLS by blocking phosphorylation of I kappa B and I kappa B kinase. Clinical use of CA may be effective in RA treatment.
机译:咖啡酸(CA)是一种酚酸,广泛存在于水果和植物中,其具有抗氧化,抗炎,抗肿瘤和免疫调节性能。因为活性氧物质(ROS)水平增加与类风湿性关节炎(RA)的发病机制有关,所以我们用Ca处理Ra-衍生的成纤维细胞样Synoviocytes(RA-FL),并研究其对细胞因子产生的影响,表达水平前列腺素E2(PGE2)和基质金属蛋白酶(MMP)-1。我们的研究结果表明,RA-FLS中高水平的Ca诱导细胞凋亡。 CA显着降低了白细胞介素(IL)-6和肿瘤坏死因子-α(TNF-alpha)中的含量。此外,PGE2和MMP-1在转录和翻译水平上显着减轻了CA显着压抑。为了揭示潜在的机制,我们将参与丝裂原激活的蛋白激酶(MAPK)和核因子Kappa-Light-Chain-Enhancer的活化B细胞(NF-Kappa B)信号传导途径的核因子Kappa轻链增强剂的蛋白质水平进行了比较发现CA通过抑制NF-Kappa B抑制剂激酶(I Kappa B激酶/ IKK)α/β和I Kappa Bα的磷酸化对细胞因子产生的调节功能。总之,本研究首次证明了Ca对抑制IL-6和TNF-α的影响,通过阻断I Kappa B和I Kappa B激酶的磷酸化来缓解RA-FL中的炎症反应。 Ca的临床应用可能在RA治疗中有效。

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