冠突散囊菌来源的2-6-H-5-B化合物的抗炎作用及机制研究

    Study on Anti-inflammatory Activity and Mechanism of Compound 2-6-H-5-B from Eurotium Cristatum

    • 摘要: 目的 研究冠突散囊菌来源的苯甲醛衍生物(2-6-H-5-B)对脂多糖诱导的RAW264.7细胞的抗炎作用及机制。方法 RAW264.7细胞经不同浓度的苯甲醛衍生物(2-6-H-5-B)(25,50和100 μmol·L-1)及阳性对照药地塞米松(0.5 μmol·L-1)预处理1 h后,除对照组外,其余各组给予100 ng·mL-1 脂多糖刺激诱导24 h。采用Griess试剂法检测NO释放水平,ELISA法分析TNF-α、IL-6和MCP-1的表达水平,以及Western blotting检测AMPK、NF-κB和MAPK信号通路的蛋白表达情况。结果 化合物2-6-H-5-B可以显著抑制活化的巨噬细胞NO(P<0.01或P<0.05)、TNF-α(P<0.01)、IL-6(P<0.01)和MCP-1 (P<0.01)的产生,表现出较好的抗炎活性。研究表明,2-6-H-5-B未能明显阻断NF-κB和MAPK信号通路的活化,但可以显著增加p-AMPK的表达。结论 2-6-H-5-B是一个较有潜力的抗炎药物先导物,其抗炎活性可能与激活AMPK通路相关。

       

      Abstract: OBJECTIVE To study the effects and mechanisms of anti-inflammatory of benzaldehyde derivatives (2-6-H-5-B) derived from Eurotium cristatum in lipopolysaccharide stimulated RAW264.7 cells. METHODS RAW264.7 cells were pretreated with benzaldehyde derivative(compound 2-6-H-5-B)(25, 50, 100 μmol·L-1) and postive control drug dexamethasone(0.5 μmol·L-1) for 1 h, then cells were treated with 100 ng·mL-1 lipopolysaccharide for 24 h except control group. The nitrite concentration in the culture medium was measured as an indicator of NO production by the Griess reagent according to the manufacturer’s protocol. The expression levels of TNF-α, IL-6 and MCP-1 in the cultured supernatant were detected by ELISA kits, and the protein expressions of AMPK, NF-κB and MAPK signaling pathways were analyzed by Western blotting. RESULTS The expression of pro-inflammatory cytokines, including TNF-α(P<0.01), IL-6(P<0.01) and MCP-1(P<0.01), as well as the production of NO(P<0.01 or P<0.05) were inhibited by compound 2-6-H-5-B. Further mechanism studies showed that 2-6-H-5-B failed to inhibit the activation of NF-κB and MAPK signaling pathways, but increased the expression of p-AMPK significantly. CONCLUSION The 2-6-H-5-B is a potential anti-inflammatory drug, and its anti-inflammatory activity may be related to the activation of AMPK pathway.

       

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