Procyanidins extracted from the litchi pericarp attenuate atherosclerosis and hyperlipidemia associated with consumption of a high fat diet in apolipoprotein-E knockout mice

被引:30
|
作者
Rong, Shuang [1 ,2 ,3 ,4 ]
Zhao, Siqi [3 ,4 ]
Xu, Kai [3 ,4 ]
Zhang, Li [5 ,6 ]
Zhao, Yanting [1 ,2 ]
Xiao, Xiao [1 ,2 ]
Bao, Wei [1 ,2 ]
Liu, Liegang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Dept Nutr & Food Hyg, Hubei Key Lab Food Nutr & Safety, Sch Publ Hlth,Tongji Med Coll, Wuhan, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, MOE Key Lab Environm & Hlth, Sch Publ Hlth, Tongji Med Coll, Wuhan, Hubei, Peoples R China
[3] Wuhan Univ Sci & Technol, Dept Nutr & Food Hyg, Sch Publ Hlth, Med Coll, Wuhan, Hubei, Peoples R China
[4] Wuhan Univ Sci & Technol, Inst Nutr & Chron Dis, Wuhan, Hubei, Peoples R China
[5] Hubei Prov Hosp Chinese Med, Wuhan 430015, Hubei, Peoples R China
[6] Hubei Prov Hosp Western Med, Wuhan 430015, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Procyanidins; Atherosclerosis; Hyperlipidemia; Liver; ApoE KO mice; NUCLEAR-RECEPTOR; CELL-LINES; FXR; METABOLISM; DEFICIENT; DISEASE; HEALTH; RATS;
D O I
10.1016/j.biopha.2017.10.139
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The beneficial effects of red wine against cardiovascular disease are associated with the abundant antioxidant polyphenols such as procyanidins. Recently, procyanidins extracted from the litchi pericarp (LPPC), a new source of procyanidins showed strong antioxidant activities in vitro, have been isolated and identified in our laboratory. The aim of present study was to investigate the anti-atherosclerotic effects of LPPC on atherosclerosis and hyperlipidemia in apolipoprotein E knockout (ApoE KO) mice fed a high fat diet (HFD, 21% fat, 0.15% cholesterol) for 24 weeks. The results showed that LPPC intervention alleviated atherosclerosis, fat accumulation and hyperlipidemia in ApoE KO mice. Furthermore, real-time RT-PCR results showed that LPPC can regulate several key genes involved in hepatic lipid homeostasis, such as increasing mRNA levels of farnesoid X receptor (FXR) and small heterodimer partner (SHP) which emerge as key regulators of lipid homeostasis at the transcriptional level, decreasing mRNA levels of 3-hydroxy-3-Methylglutaryl (HMG)-CoA reductase which mediates cholestrol biosynthesis, and up-regulating the mRNA expressions of ATP-binding cassette transporter-1 (ABCA1) which modulates cholesterol efflux. Thus, these results elucidated that LPPC could alleviate the lipid disorder especially hypercholesteromia and ameliorate atherosclerosis in ApoE-KO mice fed a WTD via regulating gene expression involved in hepatic lipid homeostasis effectively.
引用
收藏
页码:1639 / 1644
页数:6
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