Inhibition of acute lung injury by rubriflordilactone in LPS-induced rat model through suppression of inflammatory factor expression

被引:1
|
作者
Wang, Yan-Ying [1 ,2 ]
Qiu, Xin-Guang [1 ]
Ren, Hong-Liang [3 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Surg, 1 East Jianshe Rd, Zhengzhou 450000, Henan, Peoples R China
[2] Zhumadian City Cent Hosp, Zhumadian 463000, Peoples R China
[3] Zhumadian City Cent Hosp, Dept Surg, Zhumadian 463000, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2015年 / 8卷 / 12期
关键词
Edema; inflammation; interleukin; lung injury; silencer RNA; NF-KAPPA-B; IN-VIVO; MACROPHAGE; MICE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study demonstrates the effect of rubriflordilactone on lipopolysaccharide (LPS)-induced acute kidney injury in rats and MLE-15 cells. LPS administration in rats resulted in formation of edema which was inhibited by pretreatment with rubriflordilactone. The pulmonary tissues of LPS administered rats and MLE-15 cells showed a significant increase in the expression of matrix metalloproteinase-9, interleukin-6 and inducible nitric oxide synthase. However, rubriflordilactone treatment prior to LPS administration caused a significant reduction in the expression of these factors at a concentration of 10 nm/kg. Analysis of the Sirtuin 1 (Sirt1) expression revealed significant (P=0.002) reduction on exposure to LPS in MLE-15 cells. However, rubriflordilactone treatment at 10 nm/ml concentration before LPS exposure caused inhibition of LPS induced reduction in Sirt1 expression. Silencing of Sirt1 by siRNA in MLE-15 cells led to inhibition of increased Sirt1 expression by rubriflordilactone in LPS administered rats. These findings suggest that rubriflordilactone inhibits LPS induced acute lung injury in rats and MLE-15 cells through promotion of Sirt1 expression.
引用
收藏
页码:15954 / 15959
页数:6
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