Paeoniflorin improves survival in LPS-challenged mice through the suppression of TNF-α and IL-1β release and augmentation of IL-10 production

被引:84
作者
Cao, Wenjuan [1 ]
Zhang, Wei [1 ]
Liu, Jingjing [1 ]
Wang, Yuan [1 ]
Peng, Xuemei [2 ]
Lu, Daxiang [1 ]
Qi, Renbin [1 ]
Wang, Yanping [1 ]
Wang, Huadong [1 ]
机构
[1] Jinan Univ, Sch Med, Key Lab State Adm Tradit Chinese Med Peoples Repu, Dept Pathophysiol,Sch Med, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Sch Med, Affiliated Hosp 1, Dept Anesthesiol, Guangzhou 510632, Guangdong, Peoples R China
关键词
Peaoniflorin; Lipopolysaccharide; Mice; Mortality; Cytokines; TUMOR-NECROSIS-FACTOR; CARDIAC-FUNCTION; INDUCED LETHALITY; ENDOTOXEMIA; LIPOPOLYSACCHARIDE; MACROPHAGES; SEPSIS; LIVER; MODEL; SHOCK;
D O I
10.1016/j.intimp.2010.11.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lipopolysaccharide (LPS) plays an important role in Gram-negative bacteria-induced sepsis and multiple organ dysfunction syndrome, which are still the leading cause of high mortality in intensive care units. Although paeoniflorin (Pae) has reportedly exhibited anti-inflammatory effect and protection against immunological liver injury in mice, it is not known whether Pae improve survival in endotoxemic mice. The purpose of this study was to determine the effect of Pae on the mortality, multiple organ dysfunction and cytokine production in lipopolysaccharide (LPS)-treated mice. We found that pretreatment with Pae decreased mortality, reduced lung and kidney injury, decreased serum creatinine level and improve systolic function of heart in mice challenged with LPS. Further experiments showed that Pae inhibited LPS-stimulated tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) release and promoted LPS-induced interleukin-10 (IL-10) production. Our results indicate that Pae protects mice against lethal LPS challenge, at least in part, through inhibiting TNF-alpha and IL-1 beta production and accelerating IL-10 expression. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:172 / 178
页数:7
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