连俊江, 程彬峰, 高尧鑫, 张亚平, 马双平, 张彬彬, 郭丹丹, 薛寒, 冯志伟. 齐墩果酸对IL-1β诱导的SW982细胞炎症反应的抑制作用J. 药学学报, 2016,51(11): 1711-1716. doi: 10.16438/j.0513-4870.2016-0610
引用本文: 连俊江, 程彬峰, 高尧鑫, 张亚平, 马双平, 张彬彬, 郭丹丹, 薛寒, 冯志伟. 齐墩果酸对IL-1β诱导的SW982细胞炎症反应的抑制作用J. 药学学报, 2016,51(11): 1711-1716. doi: 10.16438/j.0513-4870.2016-0610
LIAN Jun-jiang, CHENG Bin-feng, GAO Yao-xin, ZHANG Ya-ping, MA Shuang-ping, ZHANG Bin-bin, GUO Dan-dan, XUE Han, FENG Zhi-wei. Inhibitory effect of oleanolic acid on inflammatory response in IL-1β-stimulated human synovial sarcoma SW982 cellsJ. Acta Pharmaceutica Sinica, 2016,51(11): 1711-1716. doi: 10.16438/j.0513-4870.2016-0610
Citation: LIAN Jun-jiang, CHENG Bin-feng, GAO Yao-xin, ZHANG Ya-ping, MA Shuang-ping, ZHANG Bin-bin, GUO Dan-dan, XUE Han, FENG Zhi-wei. Inhibitory effect of oleanolic acid on inflammatory response in IL-1β-stimulated human synovial sarcoma SW982 cellsJ. Acta Pharmaceutica Sinica, 2016,51(11): 1711-1716. doi: 10.16438/j.0513-4870.2016-0610

齐墩果酸对IL-1β诱导的SW982细胞炎症反应的抑制作用

Inhibitory effect of oleanolic acid on inflammatory response in IL-1β-stimulated human synovial sarcoma SW982 cells

  • 摘要: 在SW982细胞中,研究齐墩果酸对白细胞介素(interleukin,IL)-1β刺激的炎症因子表达的作用,并探讨其抗炎作用机制。采用MTT的方法检测齐墩果酸对SW982细胞的毒性作用;酶联免疫吸附实验(enzyme linked immunosorbent assay,ELISA)和实时荧光定量PCR(real-time PCR)实验在蛋白及mRNA水平上检测不同浓度的齐墩果酸(5、10、20 μmol·L-1)对IL-1β刺激炎症因子IL-6、IL-8和基质金属蛋白酶-1(matrix metallopeptidase-1,MMP-1)表达水平的影响;免疫印迹实验分析齐墩果酸对丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)、磷脂酰肌醇(-3)激酶/Akt(phosphatidylinositol-3-kinase/Akt,PI3K/Akt)和核转录因子-κB(nuclear transcription factor-κB,NF-κB)信号通路相关蛋白表达水平的影响。结果显示,不同浓度的齐墩果酸(≤40 μmol·L-1)对SW982细胞几乎无毒性;对IL-6、IL-8和MMP-1等炎症因子的表达有明显的抑制作用;能明显地抑制细胞外信号调节激酶(extracellular signal-related kinase,ERK)、p38、c-jun N末端激酶(c-jun N-terminal kinase,JNK)和Akt蛋白的磷酸化,并且抑制IκB-α蛋白的降解。齐墩果酸可能是通过MAPK、PI3K/Akt和NF-κB信号通路而抑制IL-1β刺激的炎症因子的表达。

     

    Abstract: To study the role of oleanolic acid on interleukin (IL)-1β-stimulated expression of inflammatory cytokines, and to explore its anti-inflammatory mechanism in SW982 cells, the toxicity of oleanolic acid on SW982 cells was detected by MTT; effects of different concentrations of oleanolic acid (5, 10, 20 μmol·L-1) on the expression of inflammatory factors IL-6, IL-8 and matrix metalloproteinase-1 (MMP-1) was tested at protein and mRNA levels. The study was performed in IL-1β-stimulated SW982 cells together with enzyme-linked immunosorbent assay (ELISA) and real-time fluorescence quantitative PCR (real-time PCR) methods; the influence of oleanolic acid on the phosphorylation of mitogen-activated protein kinase (MAPK), phosphatidyl inositol-3-kinase/Akt (PI3K/Akt) and nuclear transcription factor-κB (NF-κB) signaling pathways related protein was analyzed by Western blot. Results showed that different concentrations of oleanolic acid (≤ 40 μmol·L-1) were almost non-toxicity to SW982 cells; oleanolic acid significantly inhibited the expression of inflammatory factors in a dose-dependent manner; oleanolic acid restrained extracellular signal-related kinase (ERK), p38, c-jun N-terminal kinase (JNK) and Akt protein phosphorylation and IκB-α protein degradation obviously. The inhibition effect of oleanolic acid on inflammatory factors stimulated by IL-1β may be worked through MAPK, PI3K/Akt and NF-κB signaling pathways.

     

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