Vitexin ameliorates high fat diet-induced obesity in male C57BL/6J mice via the AMPK-mediated pathway

被引:0
|
作者
Peng, Ye [1 ]
Sun, Quancai [1 ]
Xu, Weidong [2 ]
He, Yuanqing [1 ]
Jin, Wengang [3 ]
Yuan, Li [1 ]
Gao, Ruichang [1 ,3 ]
机构
[1] Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Pharm, Zhenjiang, Jiangsu, Peoples R China
[3] Shaanxi Univ Technol, Bioresources Key Lab Shaanxi Prov, Sch Biol Sci & Engn, Hanzhong, Shaanxi, Peoples R China
关键词
ACTIVATED PROTEIN-KINASE; OXIDATIVE STRESS; PROMOTES ADIPOGENESIS; INDUCED ADIPOSITY; INFLAMMATION; MECHANISM; APOPTOSIS; EXTRACTS; INJURY;
D O I
10.1039/c9fo00148d
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitexin, a bioactive compound isolated from hawthorn leaf extracts, has been reported to exhibit many biological activities, such as anticancer, antioxidation, and adipogenesis inhibition activities. The current study explored the effects of vitexin on high fat diet (HFD)-induced obesity/adipogenesis in male C57BL/6J mice and 3T3-L1 adipocytes, as well as the underlying mechanisms thereof. Vitexin significantly mitigated HFD-induced body weight gain and adiposity. Vitexin also partially normalized serum, hepatic lipid contents, and decreased adipocyte size induced by the HFD. Consistently, there were significant effects of vitexin on important regulators of lipid metabolism, including AMP-activated protein kinase- (AMPK), CAATT element binding protein- (C/EBP), and fatty acid synthase (FAS) in white adipose tissue. Moreover, vitexin significantly inhibited fat accumulation in 3T3-L1 adipocytes, and this was totally abolished by compound C (an AMPK inhibitor). These results suggest that vitexin may prevent HFD-induced obesity/adipogenesis via the AMPK mediated pathway.
引用
收藏
页码:1940 / 1947
页数:8
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