Antiinflammatory effects of matrine in LPS-induced acute lung injury in mice

被引:221
作者
Zhang, Bo [1 ]
Liu, Zhong-Yang [2 ]
Li, Yan-Yan [2 ]
Luo, Ying [1 ]
Liu, Man-Ling [1 ]
Dong, Hai-Ying [1 ]
Wang, Yan-Xia [1 ]
Liu, Yi [1 ]
Zhao, Peng-Tao [1 ]
Jin, Fa-Guang [2 ]
Li, Zhi-Chao [1 ]
机构
[1] Fourth Mil Med Univ, Dept Pathol & Pathophysiol, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Tangdu Hosp, Dept Resp Med, Xian 710038, Peoples R China
基金
中国国家自然科学基金;
关键词
Matrine; Lipopolysaccharide; Acute lung injury; Cytokine; Reactive oxygen species; RESPIRATORY-DISTRESS-SYNDROME; MOBILITY GROUP BOX-1; INFLAMMATORY CYTOKINES; ENDOTOXIN; EXPRESSION; LETHALITY; MEDIATOR; SEPSIS; RECEPTOR; THERAPY;
D O I
10.1016/j.ejps.2011.09.020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Matrine is one of the main active components of Chinese herb Sophora flavescens Ait (Kushen), which has been demonstrated to be effective in suppressing inflammation. The aim of the present study is to investigate the effect of matrine on LPS-induced lung injury. Lung injury was assessed by histological study and wet to dry weight ratios, as well as cell count and protein content in bronchoalveolar lavage fluid. We also detected MPO activity reflecting neutrophil infiltration and MDA activity examining oxidative stress in lung tissues. Cytokines and ROS production in cells were monitored by ELISA and flow cytometry, respectively. The results showed that high dose of matrine significantly reduced the mortality rate of mice with LPS administration. Treatment with matrine improved LPS-induced lung histopathologic changes, alleviated pulmonary edema and lung vascular leak, inhibited MPO and MDA activity,and reduced the production of inflammatory mediators including TNF-alpha, IL-6 and HMGB1. In vitro, matrine administration reduced the production of ROS and inflammatory factors, which was possibly associated with inhibition of NF-kappa B. In conclusion, the current study demonstrated that matrine exhibited a protective effect on LPS-induced acute lung injury by inhibiting of the inflammatory response, which may involve the suppression of ROS and tissue oxidative stress. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:573 / 579
页数:7
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