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A novel naturally occurring salicylic acid analogue acts as an anti-inflammatory agent by inhibiting nuclear factor-kappaB activity in RAW264.7 macrophages

机译:一种新型的天然水杨酸类似物通过抑制RAW264.7巨噬细胞中的核因子-κB活性而充当抗炎药

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摘要

Methyl salicylate 2-O-β-d-lactoside (DL0309), is a molecule chemically related to salicylic acid that is isolated from Gaultheria yunnanensis (FRANCH.) REHDER (G. yunnanensis). G. yunnanensis, a traditional Chinese herbal medicine, is widely used for treating rheumatoid arthritis, swelling, pain, trauma, and chronic tracheitis. In the present study, we explored the mechanism whereby DL0309 exerts anti-inflammatory effects, using the model of lipopolysaccharide (LPS)-treated RAW264.7 cells. We examined the effects of DL0309 on LPS-induced nuclear factor-kappaB (NF-κB) activity by Western blot analysis, cell imaging analysis and an electrophoretic mobility shift assay (EMSA). Production of pro-inflammatory cytokines was also measured. Our observations indicate that DL0309 suppressed production of nitric oxide (NO), reactive oxygen species (ROS) and the pro-inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β), in a concentration-dependent manner. The phosphorylation of IKK-β and degradation of IκB-α by LPS were both inhibited by DL0309 in the cytoplasm. The increased protein level of NF-κB by LPS in the nucleus was also reduced by DL0309. Consistent with these results, we found that DL0309 prevents the nuclear translocation and DNA binding activity of NF-κB. Finally, our results demonstrate that DL0309 exerts anti-inflammatory effects, by inhibiting the production of pro-inflammatory cytokines and suppressing of the activation of the NF-κB signaling pathway in LPS-treated macrophage cells. Therefore, DL0309 may have therapeutic potential for treating inflammatory diseases by regulating the NF-κB pathway and pro-inflammatory cytokine production.
机译:水杨酸甲酯2-O-β-d-乳糖苷(DL0309)是与水杨酸化学相关的分子,该分子是从云南高地红(瑞香)中分离出来的。云南中药G. yunnanensis被广泛用于治疗类风湿关节炎,肿胀,疼痛,外伤和慢性气管炎。在本研究中,我们使用脂多糖(LPS)处理的RAW264.7细胞模型探索了DL0309发挥抗炎作用的机制。我们通过Western印迹分析,细胞成像分析和电泳迁移率变动分析(EMSA)检查了DL0309对LPS诱导的核因子-κB(NF-κB)活性的影响。还测量了促炎细胞因子的产生。我们的观察结果表明,DL0309抑制一氧化氮(NO),活性氧(ROS)和促炎细胞因子(例如肿瘤坏死因子-α(TNF-α),白介素6(IL-6)和白细胞介素-1β(IL-1β),呈浓度依赖性。 DL0309在细胞质中均抑制了IKK-β的磷酸化和LPS对IκB-α的降解。 DL0309也降低了LPS增强了核中NF-κB的蛋白质水平。与这些结果一致,我们发现DL0309阻止了NF-κB的核转运和DNA结合活性。最后,我们的结果表明,DL0309通过抑制促炎细胞因子的产生并抑制LPS处理的巨噬细胞中NF-κB信号通路的激活而发挥抗炎作用。因此,DL0309通过调节NF-κB途径和促炎性细胞因子的产生可能具有治疗炎性疾病的潜力。

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