Bio-Organic Science Division, Korea Research Institute of Chemical Technology, 100, Jangdong, Yuseong, Daejeon 305-343, Republic of Korea.
J Ethnopharmacol. 2011 Mar 24;134(2):288-93. doi: 10.1016/j.jep.2010.12.020. Epub 2010 Dec 21.
The present study was performed to investigate the underlying mechanisms of anti-inflammatory effects with the extract of Euonymus alatus (EEA), and specially focused on nuclear factor κB (NF-κB) signaling pathway by targeting the IκB kinase β (IKKβ).
The effect of EEA for IKKβ activity was analyzed using an immobilized metal affinity for phosphochemicals (IMAP)-based time-resolved fluorescence resonance energy transfer (TR-FRET) assay. The effect of EEA on lipopolysaccharide (LPS)-induced NF-κB activation in murine macrophage RAW 264.7 cells with western blotting and immunofluorescent staining was evaluated.
IKKβ studies based on IMAP-TR-FRET showed that EEA possesses a potent IKKβ inhibitory activity with IC(50) value of 11.83μg/ml. EEA (10, 30μg/ml) also attenuated the LPS-induced IκBα phosphorylation/degradation, NF-κB translocation and subsequent NO synthesis in RAW 264.7 cells.
These results suggest that EEA abrogates LPS-induced NF-κB signaling pathway by targeting the IKKβ in RAW 264.7 cells and these properties may provide a molecular basis for understanding the inhibitory effects of EEA on LPS-mediated inflammation.
本研究旨在通过靶向 IκB 激酶β(IKKβ),探讨卫矛提取物(EEA)抗炎作用的潜在机制,特别是针对核因子κB(NF-κB)信号通路。
采用基于固定化金属亲和磷酸化学物质(IMAP)的时间分辨荧光共振能量转移(TR-FRET)分析,研究 EEA 对 IKKβ 活性的影响。通过 Western blot 和免疫荧光染色评估 EEA 对脂多糖(LPS)诱导的小鼠巨噬细胞 RAW 264.7 细胞 NF-κB 激活的影响。
基于 IMAP-TR-FRET 的 IKKβ 研究表明,EEA 具有较强的 IKKβ 抑制活性,IC50 值为 11.83μg/ml。EEA(10、30μg/ml)还可减弱 LPS 诱导的 RAW 264.7 细胞中 IκBα 磷酸化/降解、NF-κB 易位和随后的 NO 合成。
这些结果表明,EEA 通过靶向 RAW 264.7 细胞中的 IKKβ 阻断 LPS 诱导的 NF-κB 信号通路,这些特性可能为理解 EEA 对 LPS 介导的炎症的抑制作用提供分子基础。