Fucosterol attenuates lipopolysaccharide-induced acute lung injury in mice

被引:27
|
作者
Li, Yuexia [1 ]
Li, Xiaohui [2 ]
Liu, Gang [1 ]
Sun, Rongqing [1 ]
Wang, Lirui [1 ]
Wang, Jing [3 ]
Wang, Hongmin [3 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Intens Care Unit, Zhengzhou 450052, Henan Province, Peoples R China
[2] Henan Prov Peoples Hosp, Dept Cardiovasc Surg, Zhengzhou, Henan Province, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Resp Med, Zhengzhou 450052, Henan Province, Peoples R China
关键词
Fucosterol; LPS; Acute lung injury; NF-kappa B; NF-KAPPA-B; RESPIRATORY-DISTRESS-SYNDROME; RAW264.7; MACROPHAGES; PELVETIA-SILIQUOSA; LPS; ACTIVATION; BINDING; PATHOPHYSIOLOGY; INFLAMMATION; INHIBITION;
D O I
10.1016/j.jss.2014.12.054
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Fucosterol has been reported to have antioxidant, antidiabetic, and anti-inflammatory effects. In this study, we investigated the protective effect and the possible mechanism of fucosterol on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice. Methods: Lung injury was assessed by a histologic study, pulmonary edema, and inflammatory cytokines production in bronchoalveolar lavage fluid. Alveolar macrophages were stimulated with LPS in the presence or absence of fucosterol. The expressions of inflammatory cytokines were determined by enzyme-linked immunosorbant assay. Nuclear factor-kappa B (NF-kappa B) expression was detected by Western blotting. Results: The results showed that fucosterol attenuated lung histopathologic changes, wet-to-dry ratio, and tumor necrosis factor-alpha, interleukin (IL)-6 and IL-1 beta production in LPS-induced ALI in mice. Meanwhile, fucosterol inhibited NF-kappa B activation and tumor necrosis factor-alpha, IL-6, and IL-1 beta production in LPS-stimulated alveolar macrophages. Conclusions: In conclusion, the present study demonstrated that fucosterol exhibited a protective effect on LPS-induced acute lung injury, and the possible mechanism is involved in inhibiting NF-kappa B activation, thereby inhibiting LPS-induced inflammatory response. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:515 / 521
页数:7
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