TLR4型
炎症
NF-κB
香烟烟雾
下调和上调
药理学
信号转导
医学
NFKB1型
免疫学
化学
生物化学
基因
转录因子
环境卫生
作者
Dan Wang,Kun Tao,Junjie Xion,Shuyun Xu,Yao‐Wen Jiang,Quan Chen,Sirong He
标识
DOI:10.1016/j.bbrc.2016.03.001
摘要
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-α in BAL fluid and lungs in a dose-dependent manner, except MCP-1, IL-1β and IFN-γ, 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-κB in lungs, suggesting that TAK-242-mediated inhibition occurred largely through the TLR4/NF-κB 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.
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