Effects of Isorhapontigenin on Lipopolysaccharide-Induced Acute Lung Injury in Mice.
10.3881/j.issn.1000-503X.14799
- Author:
Peiyu YAO
1
;
Ruibing DENG
1
;
Zhenzhu LI
1
;
Zhuo ZHANG
1
Author Information
1. Department of Emergency,Tianjin Union Medical Center,Tianjin 300121,China.
- Publication Type:Journal Article
- Keywords:
acute lung injury;
autophagy;
inflammation;
isorhapontigenin;
oxidative stress
- MeSH:
Animals;
Mice;
Acute Lung Injury/pathology*;
Beclin-1/pharmacology*;
Cyclooxygenase 2/metabolism*;
Cytokines;
HMGB1 Protein/metabolism*;
Interleukin-6;
Lipopolysaccharides;
Lung/pathology*;
NF-kappa B/metabolism*;
Reactive Oxygen Species/metabolism*;
Tumor Necrosis Factor-alpha/metabolism*
- From:
Acta Academiae Medicinae Sinicae
2022;44(5):794-801
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effect and mechanism of isorhapontigenin (ISO) in the protection of mice from the lipopolysaccharide (LPS)-induced acute lung injury (ALI). Methods RAW264.7 cells were cultured in vitro with different concentrations of ISO and the viability of the cells was measured by CCK-8 assay.Further,RAW264.7 cells were induced with 200 ng/ml LPS and then treated with ISO and the autophagy inhibitor 3-methyladenine (3-MA).Western blotting was employed to determine the expression of inflammatory cytokines [interleukin (IL)-1β,IL-6,tumor necrosis factor-α (TNF-α),P65,phospho-P56 (p-P65),IκB,phospho-IκB (p-IκB),inducible nitric oxide synthase (iNOS),cyclooxygenase-2 (COX-2),and high mobility group box-1 (HMGB1)] and autophagy markers (LC3Ⅱ/Ⅰ,Beclin1,and P62).The reactive oxygen species (ROS) production of the cells was measured with the DCFH-DA probe.The mouse model of ALI was established by intraperitoneal injection of LPS (15 mg/kg).The pathological changes of the lung tissue were observed via HE staining.The expression of inflammatory cytokines and autophagy markers in the lung tissue was determined by Western blotting and the content of ROS in bronchoalveolar lavage fluid (BALF) by flow cytometry. Results ISO down-regulated the expression of IL-1β,IL-6,TNF-α,iNOS,COX-2,and HMGB1 and inhibited the ROS production in the LPS-induced RAW264.7 cells (all P<0.05).Furthermore,it promoted the expression of LC3Ⅱ/Ⅰ and Beclin1 and inhibited the expression of P62,thereby activating autophagy (all P<0.05).However,the addition of 3-MA up-regulated the expression of p-P65/P65,p-IκB,iNOS,COX-2,and HMGB1,down-regulated that of IκB (all P<0.001),and promote the production of ROS.ISO mitigated the pathological changes in the lung tissue of ALI mice.It down-regulated the expression of p-P65/P65,p-IκB,iNOS,COX-2,and HMGB1 and up-regulated that of IκB in the lung tissue (all P<0.001) and decreased the ROS production in BALF.However,such protective effect was reversed by 3-MA. Conclusion ISO may induce autophagy of macrophages to protect mice from LPS-induced ALI.
