黄芩素
上睑下垂
药理学
医学
免疫印迹
肺
脂多糖
蛋白激酶B
免疫学
炎症
化学
细胞凋亡
内科学
炎症体
生物化学
基因
作者
Zhi-dan Gao,Haidong Yan,Ning‐hua Wu,Qing Yao,Bin-bin Wan,Xiufen Liu,Zhen-wang Zhang,Qingjie Chen,Huang Cui-ping
标识
DOI:10.1016/j.pupt.2022.102121
摘要
Acute lung injury is an acute progressive respiratory failure caused by several of non-cardiogenic factors which involves in excessive amplification or uncontrolled inflammatory response.In this study, we investigated the protective effect of baicalein against acute lung injury induced by LPS and explored the underlying mechanisms.Forty-eight SPF male C57BL/6 mice were randomly divided into normal group, model group, dexamethasone group and baicalein low-dose, medium-dose and high-dose groups. After 5 days of adaptive feeding, the mice were intraperitoneally injected with LPS and dissected after 12 h. Hematoxylin-eosin staining, ELISA assay, immunofluorescence assay and Western-Blot were applied to appraise microstructural changes and protein expressions of lung tissues. Systems pharmacology study was used to evaluate the protection of baicalein on acute lung injury.The results showed that baicalein administration could significantly inhibit LPS-induced lung morphological changes, inhibit inflammatory response and pyroptosis. A total of forty-three potential targets of baicalein and acute lung injury were obtained. And PI3K-Akt, TNF and NF-κB were mainly signaling pathways. It is worth mentioning that this experiment also confirmed that NLRP3, caspase-1 and other inflammasome are involved in pyroptosis.Baicalein has protected against LPS-induced lung tissues injury via inhibiting inflammatory response and pyroptosis.
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