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Daidzein attenuates lipopolysaccharide-induced acute lung injury via toll-like receptor 4/NF-kappaB pathway

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机构: [a]Department of Anesthesiology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, PR China [b]Department of Anesthesiology, The Affiliated Hospital of Xuzhou Medical College, Xuzhou 221002, PR China [c]Department of Anesthesiology, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, PR China [d]Department of Anesthesiology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China
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关键词: Acute lung injury Acute respiratory distress syndrome Daidzein Lipopolysaccharide Toll-like receptor 4 NF-kappaB

摘要:
Daidzein, a diphenolic isoflavone from many plants and herbs, has been reported to have anti-inflammatory properties. However, the effects of daidzein on lipopolysaccharide (LPS)-induced acute lung injury have not been determined. The aim of this study was to detect the effects of daidzein on LPS-induced acute lung injury and investigate the molecular mechanisms. Daidzein was intraperitoneally injected (2, 4, 8 mg/kg) 30 min after intratracheal instillation of LPS (5 mg/kg) in rats. The results showed that daidzein treatment remarkably improved the pulmonary histology and decreased the lung wet/dry weight ratios. We also found that daidzein significantly inhibited LPS-induced increases of macrophages and neutrophils infiltration of lung tissues, as well as markedly attenuated MPO activity. Moreover, daidzein effectively reduced the inflammatory cytokines release and total protein in bronchoalveolar lavage fluids (BALF). Furthermore, daidzein significantly inhibited LPS-induced toll-like receptor 4 (TLR4) and myeloid differentiation factor 88 (MyD88) protein up-expressions and NF-kappa B activation in lung tissues. In vitro, daidzein obviously inhibited the expressions of TLR4 and MyD88 and the activation of NF-kappa B in LPS-stimulated A549 alveolar epithelial cells. In conclusion, these data indicate that the anti-inflammatory effects of daidzein against LPS-induced ALI may be due to its ability to inhibit TLR4-MyD88-NF-kappa B pathway and daidzein may be a potential therapeutic agent for LPS-induced ALL (C) 2015 Elsevier B.V. All rights reserved.

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出版当年[2014]版:
大类 | 3 区 医学
小类 | 3 区 药学 4 区 免疫学
最新[2023]版:
大类 | 2 区 医学
小类 | 2 区 免疫学 2 区 药学
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出版当年[2013]版:
Q2 PHARMACOLOGY & PHARMACY Q3 IMMUNOLOGY
最新[2023]版:
Q1 PHARMACOLOGY & PHARMACY Q2 IMMUNOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2013版] 出版当年五年平均 出版前一年[2012版] 出版后一年[2014版]

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第一作者机构: [a]Department of Anesthesiology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, PR China [b]Department of Anesthesiology, The Affiliated Hospital of Xuzhou Medical College, Xuzhou 221002, PR China
通讯作者:
通讯机构: [*1]Party Secretary Office, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, PR China.
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