A novel pentacyclic triterpenoid, Ilexgenin A, shows reduction of atherosclerosis in apolipoprotein E deficient mice

被引:35
|
作者
Liu, Chang [1 ,2 ]
Zhao, Junxian [2 ]
Liu, YunXing [1 ]
Huang, Yi [3 ]
Shen, Yanjun [1 ]
Wang, Juan [2 ]
Sun, Weidong [2 ,4 ,5 ]
Sun, Yun [1 ,2 ]
机构
[1] Yangzhou Univ, Coll Med, Yangzhou 225001, Jiangsu, Peoples R China
[2] Yangzhou Univ, Med & Pharmaceut Inst, 11 Huaihai Rd, Yangzhou 225001, Jiangsu, Peoples R China
[3] Suzhou Vocat Hlth Coll, Suzhou 215009, Jiangsu, Peoples R China
[4] Chinese Med Hosp Yangzhou City, Yangzhou 225009, Jiangsu, Peoples R China
[5] Yangzhou Univ, Inst Clin Chinese Tradit Med, Yangzhou 225001, Jiangsu, Peoples R China
关键词
Ilexgenin A; Atherosclerosis; Lipid disorder; Inflammation; THP-1; Oxidized low-density lipoprotein; NF-KAPPA-B; HIGH-DENSITY-LIPOPROTEIN; CORONARY-HEART-DISEASE; STATIN THERAPY; CHOLESTEROL; ACTIVATION; MACROPHAGE; ATORVASTATIN; INHIBITORS; MONOCYTE;
D O I
10.1016/j.intimp.2016.08.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ilexgenin A (IA), a novel pentacyclic triterpenoid, is a compound extracted from leaves of Ilex hainanensis Merr. In this study, we explored the efficacy of IA on atherosclerosis and its underlying mechanism. We determined that treatment with IA attenuated atherosclerosis in high-fat diet-induced apolipoprotein E deficient mice via a series of effects involving regulation of lipid parameters, decrease of atherosclerosis-related indexes, inhibition of inflammatory cytokines secretion and pathological changes of main organs. Furthermore, the underlying mechanism of IA was investigated on oxidized low-density lipoprotein (Ox-LDL)-induced THP-1 cells. We showed that pre-treatment with IA decreased active inflammation cytokines involving interleukin-6 (IL-6), IL-1 and tumor necrosis factor-alpha (TNF-alpha) expression in a concentration-dependent manner. In addition, we confirmed that IA inhibited the phosphatidylinositol 3-kinase (PI3K), protein kinase B (Akt), IKK alpha phosphorylation and NF-kappa B activity induced by Ox-LDL Overall, these findings define IA as a novel drug candidate for anti-atherosclerotic therapy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 124
页数:10
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