Bufei Yishen formula protects the airway epithelial barrier and ameliorates COPD by enhancing autophagy through the Sirt1/AMPK/Foxo3 signaling pathway

被引:2
|
作者
Jia, Lidan [1 ,2 ]
Liu, Xuefang [1 ,2 ,3 ]
Liu, Xinguang [1 ,2 ,3 ]
Guan, Qingzhou [1 ,2 ,3 ]
Tian, Yange [1 ,2 ,3 ]
Li, Jiansheng [1 ,2 ,4 ]
Zhao, Peng [1 ,2 ,3 ]
机构
[1] Henan Univ Chinese Med, Henan Key Lab Chinese Med Resp Dis, Zhengzhou 450046, Henan Province, Peoples R China
[2] Collaborat Innovat Ctr Chinese Med & Resp Dis Coco, Zhengzhou 450046, Henan Province, Peoples R China
[3] Henan Univ Chinese Med, Acad Chinese Med Sci, Zhengzhou 450000, Peoples R China
[4] Henan Univ Chinese Med, Dept Resp Dis, Affiliated Hosp 1, Zhengzhou 450000, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic obstructive pulmonary disease; Bufei Yishen formula; Airway epithelial barrier; SIRT1/AMPK/FOXO3; signals; Autophagy; OBSTRUCTIVE PULMONARY-DISEASE; IMPAIRMENT; CELLS;
D O I
10.1186/s13020-024-00905-1
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
ObjectBufei Yishen formula (BYF), a traditional Chinese medicine alleviates COPD symptoms and suppresses airway epithelial inflammation. In this study, we determined whether BYF protects the airway epithelial barrier from destruction in COPD rats.MethodsThe protective effects of BYF on the airway epithelial barrier were examined in a rat COPD model. BEAS-2B epithelial cells were exposed to cigarette smoke extract (CSE) to determine the effect of BYF on epithelial barrier function. Transcriptomic and network analyses were conducted to identify the protective mechanisms.ResultsOral BYF reduced the severity of COPD in rats by suppressing the decline in lung function, pathological changes, inflammation, and protected airway epithelial barrier function by upregulating apical junction proteins, including occludin (OCLN), zonula occludens (ZO)-1, and E-cadherin (E-cad). BYF treatment reduced epithelial permeability, and increased TEER as well as the apical junction proteins, OCLN, ZO-1, and E-cad in BEAS-2B cells exposed to CSE. Furthermore, 58 compounds identified in BYF were used to predict 421 potential targets. In addition, the expression of 572 differentially expressed genes (DEGs) was identified in CSE-exposed BEAS-2B cells. A network analysis of the 421 targets and 572 DEGs revealed that BYF regulates multiple pathways, of which the Sirt1, AMPK, Foxo3, and autophagy pathways may be the most important with respect to protective mechanisms. Moreover, in vitro experiments confirmed that nobiletin, one of the active compounds in BYF, increased apical junction protein levels, including OCLN, ZO-1, and E-cad. It also increased LC3B and phosphorylated AMPK levels and decreased the phosphorylation of FoxO3a.ConclusionsBYF protects the airway epithelial barrier in COPD by enhancing autophagy through regulation of the SIRT1/AMPK/FOXO3 signaling pathway.
引用
收藏
页数:15
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