Alisol A Alleviates Arterial Plaque by Activating AMPK/SIRT1 Signaling Pathway in apoE-Deficient Mice

被引:16
|
作者
Wang, Ke [1 ]
Zhang, Beibei [1 ]
Song, Dingzhong [1 ]
Xi, Jianqiang [1 ]
Hao, Wusi [1 ]
Yuan, Jie [1 ]
Gao, Chenyu [1 ]
Cui, Zhongbao [1 ]
Cheng, Zhihong [1 ]
机构
[1] China State Inst Pharmaceut Ind, Natl Pharmaceut Engn & Res Ctr, Shanghai, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2020年 / 11卷
关键词
Alisol A; AMPK/SIRT1; pathway; anti-atherogenesis; anti-inflammation; PPAR alpha/delta; APOLIPOPROTEIN-E; PPAR-ALPHA; ATHEROSCLEROSIS; METABOLISM; RECEPTOR; INFLAMMATION; REDUCE; SIRT1;
D O I
10.3389/fphar.2020.580073
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alismatis Rhizoma (zexie), an herb used in traditional Chinese medicine, exhibits hypolipemic, anti-inflammation and anti-atherosclerotic activities. Alisol A is one of the main active ingredients in Alismatis Rhizoma extract. In this study, we investigate the role of alisol A in anti-atherosclerosis (AS). Our study demonstrated that alisol A can effectively inhibit the formation of arterial plaques and blocked the progression of AS in ApoE(-/-) mice fed with high-fat diet and significantly reduced the expression of inflammatory cytokins in aorta, including ICAM-1, IL-6, and MMP-9. In addition, we found that alisol A increased the expression of PPAR alpha and PPAR delta proteins in HepG2 cells and in liver tissue from ApoE(-/-) mice. Alisol A activated the AMPK/SIRT1 signaling pathway and NF-kappa B inhibitor I kappa B alpha in HepG2 cells. Our results suggested that alisol A is a multi-targeted agent that exerts anti-atherosclerotic action by regulating lipid metabolism and inhibiting inflammatory cytokine production. Therefore, alisol could be a promising lead compound to develop drugs for the treatment of AS.
引用
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页数:10
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