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TAK-242 attenuates acute cigarette smoke-induced pulmonary inflammation in mouse via the TLR4/NF-kappa B signaling pathway

机译:TAK-242通过TLR4 /NF-κB信号传导通路减轻小鼠的急性香烟烟雾诱发的肺部炎症

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The present study determined the effect of TAK-242 on attenuating acute cigarette smoke induced pulmonary inflammation and attempted to dissect its underlying mechanisms of action. When administered to the C57BL/6J mice after a 3 days period of cigarettes exposure,TAK-242 significantly decreased the accumulation of macrophages, neutrophils, lymphocytes and DCs, and upregulation of IL-6, IL-8 and TNF-alpha in BAL fluid and lungs in a dose-dependent manner, except MCP-1, IL-1 beta and IFN-gamma, which demonstrated that TAK-242 inhibits release of various inflammatory mediators induced by cigarette smoke. TAK-242 also significantly suppressed the expression of TLR4, MyD88 and the activation of NF-kappa B in lungs, suggesting that TAK-242-mediated inhibition occurred largely through the TLR4/NF-kappa B signal pathway. Our results support TAK-242 as a potent therapeutic agent in the treatment of cigarette smoke induced-pulmonary inflammation, and warrants further pharmaceutical investigation. (C) 2016 Elsevier Inc. All rights reserved.
机译:本研究确定了TAK-242对减轻急性香烟烟雾引起的肺部炎症的作用,并试图剖析其潜在的作用机制。在经过三天的香烟暴露后向C57BL / 6J小鼠给药时,TAK-242显着降低了巨噬细胞,嗜中性粒细胞,淋巴细胞和DC的积累,以及BAL液中IL-6,IL-8和TNF-α的上调除了MCP-1,IL-1β和IFN-γ外,它和肺部呈剂量依赖性,这表明TAK-242抑制香烟烟雾诱导的各种炎症介质的释放。 TAK-242还显着抑制肺中TLR4,MyD88的表达和NF-κB的激活,这表明TAK-242介导的抑制作用主要通过TLR4 /NF-κB信号途径发生。我们的研究结果支持TAK-242作为治疗香烟烟雾诱发的肺部炎症的有效治疗剂,值得进一步进行药物研究。 (C)2016 Elsevier Inc.保留所有权利。

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