Xuebijing alleviates LPS-induced acute lung injury by downregulating pro-inflammatory cytokine production and inhibiting gasdermin-E-mediated pyroptosis of alveolar epithelial cells

被引:0
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作者
ZHANG Cuiping [1 ]
CHEN Xiaoyan [1 ]
WEI Tianchang [1 ]
SONG Juan [1 ]
TANG Xinjun [1 ]
BI Jing [1 ]
CHEN Cuicui [1 ]
ZHOU Jian [1 ]
SU Xiao [2 ]
SONG Yuanlin [1 ,3 ,4 ,5 ,6 ]
机构
[1] Shanghai Key Laboratory of Lung Inflammation and Injury,Department of Pulmonary Medicine,Zhongshan Hospital,Fudan University
[2] The Unit of Respiratory Infection and Immunity,Institut Pasteur of Shanghai,Chinese Academy of Sciences
[3] Shanghai Institute of Infectious Disease and Biosecurity
[4] Shanghai Respiratory Research Institute
[5] National Clinical Research Center for Aging and Medicine,Huashan Hospital,Fudan University
[6] Department of Pulmonary Medicine,Jinshan Hospital of Fudan
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中图分类号
R285 [中药药理学];
学科分类号
摘要
Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) is characterized by diffuse alveolar injury primarily caused by an excessive inflammatory response.Regrettably,the lack of effective pharmacotherapy currently available contributes to the high mortality rate in patients with this condition.Xuebijing (XBJ),a traditional Chinese medicine recognized for its potent anti-inflammatory properties,exhibits promise as a potential therapeutic agent for ALI/ARDS.This study aimed to explore the preventive effects of XBJ on ALI and its underlying mechanism.To this end,we established an LPS-induced ALI model and treated ALI mice with XBJ.Our results demonstrated that pre-treatment with XBJ significantly alleviated lung inflammation and increased the survival rate of ALI mice by 37.5%.Moreover,XBJ substantially suppressed the production of TNF-α,IL-6,and IL-1β in the lung tissue.Subsequently,we performed a network pharmacology analysis and identified identified 109 potential target genes of XBJ that were mainly involved in multiple signaling pathways related to programmed cell death and anti-inflammatory responses.Furthermore,we found that XBJ exerted its inhibitory effect on gasdermin-E-mediated pyroptosis of lung cells by suppressing TNF-α production.Therefore,this study not only establishes the preventive efficacy of XBJ in ALI but also reveals its role in protecting alveolar epithelial cells against gasdermin-E-mediated pyroptosis by reducing TNF-α release.
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页码:576 / 588
页数:13
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