免疫印迹
TLR4型
NF-κB
信号转导
NFKB1型
药理学
免疫学
医学
αBκ
病毒
炎症
生物
生物化学
转录因子
基因
作者
Lanying Ma,Tong Wang,Meiyi Liu,Lingyun Ji,Yanan Wang,Shuting Li,Yanan Zhang,Yuan Wang,Wenxiao Zhao,Zhichun Wu,Huayun Yu,Haijun Zhao
标识
DOI:10.1016/j.jep.2024.118000
摘要
Xiaoer Niuhuang Qingxin Powder (XNQP) is a classic traditional Chinese medicine formula with significant clinical efficacy for treating febrile convulsions and influenza. This study aims to explore the potential mechanisms of XNQP in combating combating the influenza A virus, providing a theoretical basis for its clinical application. The present investigation employed network pharmacology and bioinformatics analysis to determine the TLR4/MYD88/NF-κB signaling pathway as a viable target for XNQP intervention in IAV infection.Subsequently, a mouse model of influenza A virus infection was established, and different doses of XNQP were used for intervention. The protein expression levels of TLR4/MYD88/NF-κB were detected using HE staining, Elisa, immunohistochemistry, immunofluorescence, and western blot. The results showed that treatment with XNQP after IAV infection reduced the mortality and prolonged the survival time of infected mice. It reduced the release of TNF-α and IFN-γ in the serum and alleviated pathological damage in the lung tissue following infection. Additionally, the levels of TLR4, MyD88, NF-κB, and p–NF–κB P65 proteins were significantly reduced in lung tissue by XNQP. The inhibitory effect of XNQP on the expression of MyD88 and NF-κB was antagonized when TLR4 signaling was overexpressed. Consequently, the expression levels of MyD88, NF-κB, and p–NF–κB P65 were increased in lung tissue. Conversely, the expression levels of the proteins MyD88, NF-κB, and p–NF–κB P65 were downregulated when TLR4 signaling was inhibited. XNQP alleviated lung pathological changes, reduced serum levels of inflammatory factors, reduced mortality, and prolonged survival time in mice by inhibiting the overexpression of the TLR4/MyD88/NF-κB signaling pathway in lung tissues after IAV infection.
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