Platycodon grandiflorus Root Extract Attenuates Body Fat Mass, Hepatic Steatosis and Insulin Resistance through the Interplay between the Liver and Adipose Tissue

被引:30
|
作者
Kim, Ye Jin [1 ,2 ]
Choi, Ji-Young [1 ,2 ]
Ryu, Ri [1 ,2 ]
Lee, Jeonghyeon [1 ,2 ]
Cho, Su-Jung [1 ,2 ]
Kwon, Eun-Young [1 ,2 ]
Lee, Mi-Kyung [3 ]
Liu, Kwang-Hyeon [4 ,5 ]
Rina, Yu [6 ]
Sung, Mi-Kyung [7 ]
Choi, Myung-Sook [1 ,2 ]
机构
[1] Kyungpook Natl Univ, Ctr Food & Nutr Genom Res, 1370 San Kyuk Dong, Daegu 41566, South Korea
[2] Kyungpook Natl Univ, Dept Food Sci & Nutr, 1370 San Kyuk Dong, Taegu 702701, South Korea
[3] Sunchon Natl Univ, Dept Food & Nutr, Sunchon 540950, South Korea
[4] Kyungpook Natl Univ, Coll Pharm, 1370 San Kyuk Dong, Taegu 702701, South Korea
[5] Kyungpook Natl Univ, Pharmaceut Sci Res Inst, 1370 San Kyuk Dong, Taegu 702701, South Korea
[6] Univ Ulsan, Dept Food Sci & Nutr, Ulsan 44610, South Korea
[7] Sookmyung Womens Univ, Dept Food & Nutr, Seoul 04310, South Korea
来源
NUTRIENTS | 2016年 / 8卷 / 09期
基金
新加坡国家研究基金会;
关键词
Platycodon grandiflorus root; obesity; free fatty acid oxidation; energy expenditure; thermogenesis; PPAR-GAMMA; OBESITY; INFLAMMATION; SIRT1; MICE; DISEASE; GLUCOSE; ALPHA; THERMOGENESIS; PGC-1-ALPHA;
D O I
10.3390/nu8090532
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The Platycodon grandiflorus root, a Korean medicinal food, is well known to have beneficial effects on obesity and diabetes. In this study, we demonstrated the metabolic effects of P. grandiflorus root ethanol extract (PGE), which is rich in platycodins, on diet-induced obesity. C57BL/6J mice (four-week-old males) were fed a normal diet (16.58% of kilocalories from fat), high-fat diet (HFD, 60% of kilocalories from fat), and HFD supplemented with 5% (w/w) PGE. In the HFD-fed mice, PGE markedly suppressed the body weight gain and white fat mass to normal control level, with simultaneous increase in the expression of thermogenic genes (such as SIRT1, PPAR, PGC1, and UCP1), that accompanied changes in fatty acid oxidation (FAO) and energy expenditure. In addition, PGE improved insulin sensitivity through activation of the PPAR expression, which upregulates adiponectin while decreasing leptin gene expression in adipocytes. Furthermore, PGE improved hepatic steatosis by suppressing hepatic lipogenesis while increasing expression of FAO-associated genes such as PGC1. PGE normalized body fat and body weight, which is likely associated with the increased energy expenditure and thermogenic gene expression. PGE can protect from HFD-induced insulin resistance, and hepatic steatosis by controlling lipid and glucose metabolism.
引用
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页数:10
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