1-Deoxynojirimycin isolated from Bacillus subtilis improves hepatic lipid metabolism and mitochondrial function in high-fat-fed mice

被引:50
作者
Do, Hyun Ju [1 ]
Chung, Ji Hyung [2 ]
Hwang, Ji Won [1 ,3 ]
Kim, Oh Yoen [4 ]
Lee, Jae-Yeon [5 ]
Shin, Min-Jeong [1 ,3 ,6 ]
机构
[1] Korea Univ, Dept Food & Nutr, Seoul 136704, South Korea
[2] CHA Univ, Dept Appl Biosci, Gyeonggi Do 463400, South Korea
[3] Korea Univ, Grad Sch, Dept Publ Hlth Sci, Seoul 136703, South Korea
[4] Dong A Univ, Dept Food Sci & Nutr, Pusan, South Korea
[5] Biotopia Co Ltd, R&D Ctr Nat Sci, Chunchon 200883, South Korea
[6] Korea Univ, Korea Univ Guro Hosp, Seoul 152703, South Korea
基金
新加坡国家研究基金会;
关键词
DNJ; Obesity; Lipogenesis; Mitochondria; AMPK; BINDING-PROTEIN-BETA; INSULIN-RESISTANCE; ADIPOCYTE DIFFERENTIATION; ALPHA-GLUCOSIDASE; INHIBITOR; 1-DEOXYNOJIRIMYCIN; MULBERRY; TRANSCRIPTIONAL CONTROL; COACTIVATOR PGC-1; SKELETAL-MUSCLE; LIVER-DISEASE;
D O I
10.1016/j.fct.2014.11.001
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The aim of this study was to determine whether 1-deoxynojirimycin (DNJ) isolated from Bacillus subtilis MORI beneficially influences lipid metabolism and mitochondrial function in the liver of mice fed a high-fat diet in addition to the anti-obesity properties of DNJ. Male C57BL/6 mice (n = 29; 5 weeks old) were randomly assigned to three groups: normal control diet (CTL, n = 10), high-fat diet (HF, n = 10), and high-fat diet supplemented with DNJ (DNJ, n = 9). After 12 weeks, the HF group exhibited higher overall weight gain, of the liver, and of various fat pads than the CTL and DNJ groups did. The HF group also showed greater expression of C/EBP alpha and CD36 mRNA in the liver than that in the CTL and/or DNJ groups. In addition, mRNA expressions of AAC and FAS were lower, while mRNA expression of PGC-1 beta was higher in the liver of the DNJ group than that of the HF group. The hepatic expression of p-AMPK/AMPK was higher in the DNJ group than in the HF group. This study provides novel insight into the protective effect of DNJ supplementation against obesity-induced hepatic lipid abnormalities and mitochondrial dysfunction. (C) 2014 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 7
页数:7
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