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  2. Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms

Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms

  • Biomed Eng Online. 2021 Dec 14;20(1):125. doi: 10.1186/s12938-021-00965-6.
Jinlin Ge 1 Huanhuan Yang 1 Yufeng Zeng 1 Yunjie Liu 2
Affiliations

Affiliations

  • 1 Department of Pulmonary and Critical Care Medicine, Wenzhou Hospital of Integrated Traditional Chinese and Western Medicine, Wenzhou, 325000, Zhejiang Province, China.
  • 2 Department of Respiratory and Critical Care Medicine, The Second People's Hospital of Nantong, 298 Xinhua Road, Chongchuan District, Nantong, 226002, Jiangsu, China. liuyunjie18@126.com.
Abstract

Background: Wogonin (5, 7-dihydroxy-8-methoxyflavone) is a natural di-hydroxyl flavonoid extracted from the root of Scutellaria baicalensis Georgi. This paper was intended to investigate the mechanism of action of wogonin in alleviating the inflammation and Apoptosis in acute lung injury (ALI).

Materials and methods: Lipopolysaccharide (LPS) was used to establish the in vitro model of ALI. After wogonin treatment, the cell viability and Apoptosis of LPS-induced A549 cells were, respectively, measured by CCK-8, TUNEL assays and acridine orange/ethidium bromide dual staining, while the contents of inflammatory cytokines and oxidative stress markers were estimated by RT-qPCR, ELISA assay, western blot analysis and commercial kits. Western blot was also conducted to assess the expression of proteins involved. Subsequently, the effect of wogonin on the Sirtuin 1 (SIRT1)-mediated high-mobility group box 1 protein (HMGB1) deacetylation was investigated. SIRT1 Inhibitor EX527 was used to evaluate the regulatory effects of wogonin on SIRT1-mediated HMGB1 deacetylation in A549 cells under LPS stimulation.

Results: LPS induced inflammation, oxidative stress and Apoptosis of A549 cells, which was abolished by wogonin. It was also found that wogonin promoted the HMGB1 deacetylation, accompanied by upregulated SIRT1 expression. However, SIRT1 Inhibitor EX527 partially reversed the protective effects of wogonin on the inflammation and Apoptosis of LPS-induced A549 cells.

Conclusion: Wogonin alleviated the inflammation and Apoptosis in LPS-induced A549 cells by SIRT1-mediated HMGB1 deacetylation, which might represent the identification of a novel mechanism by which wogonin exerts protective effects on ALI and provide ideas for the application of wogonin to ALI treatment.

Keywords

Acute lung injury; HMGB1 deacetylation; Inflammation; SIRT1; Wogonin.

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