Protective effect of total saponins of Aralia elata (Miq) Seem on lipopolysaccharide-induced cardiac dysfunction via down-regulation of inflammatory signaling in mice

被引:11
作者
Chen, Rong-Chang [1 ]
Wang, Jian [2 ]
Yu, Ying-Li [1 ]
Sun, Gui-Bo [1 ]
Sun, Xiao-Bo [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll, Inst Med Plant Dev, Beijing 100094, Peoples R China
[2] Harbin Univ Commerce, Res Ctr Life Sci & Environm Sci, Harbin 150028, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; NECROSIS-FACTOR-ALPHA; ACUTE LUNG INJURY; NITRIC-OXIDE; DIABETIC CARDIOMYOPATHY; OLEANOLIC ACID; SEPSIS; FAILURE; CARDIOMYOCYTES; TRANSDUCTION;
D O I
10.1039/c4ra16353b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aralia elata (Miq) Seem is widely used in folk medicine for treating various types of diseases, including diabetes, gastric ulcers, hepatitis and rheumatoid arthritis. The present study investigates the therapeutic effects and possible mechanisms of the total saponins of A. elata (Miq) Seem (TAS) against lipopolysaccharide (LPS)-induced septic cardiac dysfunction and inflammation in mice. Mice were intragastrically administrated with TAS (35, 70 and 140 mg kg(-1)) for one week before LPS challenge (10 mg kg(-1), i.p.). Cardiac injury was evaluated 6 h after LPS induction. Six hours of LPS administration deteriorated cardiac function which was attenuated by TAS pretreatment. TAS attenuated LPS-induced the increase of LDH, CK, AST, and cTnI activities in mice. TAS also ameliorated the imbalance between iNOS and eNOS, as well as preventing NF-kappa B activation and the subsequent myocardial inflammatory responses in endotoxemic mice. TAS could significantly downregulate LPS-mediated NOX2 expression and ROS production, even though TAS had no effect on LPS-activated TLR-4. The effects of TAS were closely associated with PI3K/AKT and MAPK signaling pathways, as characterized by TAS-induced activation in phospho-Akt and inhibition in phospho-ERK1/2, phospho-JNK, and phospho-P38. Besides, TAS also extended the lifespan of the toxemic mice. These results showed that TAS significantly attenuated LPS-induced cardiac dysfunction and production of inflammatory mediators by inhibiting NFkB activation, indicating TAS as a potential therapeutic agent for septic cardiac dysfunction.
引用
收藏
页码:22560 / 22569
页数:10
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