Effects of Yeast Hydrolysate on Hepatic Lipid Metabolism in High-Fat-Diet-Induced Obese Mice: Yeast Hydrolysate Suppresses Body Fat Accumulation by Attenuating Fatty Acid Synthesis

被引:20
|
作者
Jung, Eun Young [1 ]
Hong, Yang-Hee [2 ]
Kim, Jae Hwan [1 ]
Park, Yooheon [1 ]
Bae, Song Hwan [4 ]
Chang, Un Jae [3 ]
Suh, Hyung Joo [1 ]
机构
[1] Korea Univ, Dept Food & Nutr, Seoul 136703, South Korea
[2] Korea Univ, Res Inst Hlth & Sci, Seoul 136703, South Korea
[3] Dongduk Womens Univ, Dept Food & Nutr, Seoul, South Korea
[4] Hankyong Natl Univ, Dept Food & Biotechnol, Anseong, South Korea
关键词
Yeast hydrolysate; Ghrelin; Epididymal fat; Glucose-6-phosphate dehydrogenase; Malic enzyme; VISCERAL OBESITY; IMMUNOREACTIVITY; SUBSTRATE; LIVER;
D O I
10.1159/000338441
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: We observed whether the anti-obesity activity of yeast hydrolysate (YH) was due to the alteration of lipid-regulating enzyme activities. Methods: Male ICR mice were divided into four groups: a normal diet group (ND; 4.2% fat), a high-fat diet group (HF; 27.7% fat), an HF group treated orally with 0.5% or 1% YH in the drinking water (HF+YH0.5; 27.7% fat and HF+YH1; 27.7% fat). Results: After 5 weeks, the YH groups (HF+YH0.5 = 3.92 +/- 0.17 g/100 g BW and HF+YH1 = 3.76 +/- 0.13 g/100 g BW) had significantly lower levels of epididymal fats compared to the HF group (4.91 +/- 0.29 g/100 g BW; p<0.05). YH supplementation produced a decrease in serum triglycerides and low-density lipoprotein cholesterol concentrations and body weight gain, and produced a dose-dependent significant increase in serum ghrelin compared with the HF group (p<0.05). Hepatic glucose-6-phosphate dehydrogenase (G6PD) activity was inhibited by YH supplementation compared with the HF group, and mice treated orally with 1% YH exhibited a significant decrease in hepatic malic enzyme (ME) activity compared to obese mice treated with the vehicle (HF = 10.44 +/- 2.74 nmol/min/mg protein vs. HF+YH1 = 6.68 +/- 2.23 nmol/min/mg protein; p<0.05). Conclusions: YH supplementation suppressed body fat accumulation by attenuating fatty acid synthesis through the downregulation of hepatic G6PD and ME activities. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:89 / 94
页数:6
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