Suppression by licorice flavonoids of abdominal fat accumulation and body weight gain in high-fat diet-induced obese C57BL/6J mice

被引:96
作者
Aoki, Fumiki
Honda, Shinichi
Kishida, Hideyuki
Kitano, Mitsuaki
Arai, Naoki
Tanaka, Hozumi
Yokota, Shinichi
Nakagawa, Kaku
Asakura, Tomiko
Nakai, Yuji
Mae, Tatsumasa
机构
[1] Kaneka Corp, Funct Food Ingredients Div, Takasago, Hyogo 6768688, Japan
[2] Kaneka Corp, Life Sci Res Labs, Life Sci RD Ctr, Takasago, Hyogo 6768688, Japan
[3] Atomi Univ, Fac Management, Niiza, Saitama 3528501, Japan
[4] Univ Tokyo, Agr Bioinformat Res Unit, Grad Sch Agr & LIfe Sci, Bunkyo Ku, Tokyo 1138657, Japan
关键词
licorice flavonoid; diet-induced obesity; DNA microarray; metabolic syndrome;
D O I
10.1271/bbb.60463
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
We applied licorice. flavonoid oil (LFO) to high-fat diet-induced obese C57BL/6J mice and investigated its effect. LFO contains hydrophobic flavonoids obtained from licorice by extraction with ethanol. The oil is a mixture of medium-chain triglycerides, having glabridin, a major flavonoid of licorice, concentrated to 1.2% (w/w). Obese mice were fed on a high-fat diet containing LFO at 0 (control), 0.5%, 1.0%, or 2.0% for 8 weeks. Compared with mice in the control group, those in the 1% and 2% LFO groups efficiently reduced the weight of abdominal white adipose tissues and body weight gain. A histological examination revealed that the adipocytes became smaller and the fatty degenerative state of the hepatocytes was improved in the 2% LFO group. A DNA microarray analysis of the liver showed up-regulation of those genes for beta-oxidation and down-regulation of those for fatty acid synthesis in the 2% LFO group. These findings suggest that LFO prevented and ameliorated diet-induced obesity via the regulation of lipid metabolism-related gene expression in the liver.
引用
收藏
页码:206 / 214
页数:9
相关论文
共 34 条
[1]   Sesamin, a sesame lignan, is a potent inducer of hepatic fatty acid oxidation in the rat [J].
Ashakumary, L ;
Rouyer, I ;
Takahashi, Y ;
Ide, T ;
Fukuda, N ;
Aoyama, T ;
Hashimoto, T ;
Mizugaki, M ;
Sugano, M .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1999, 48 (10) :1303-1313
[2]   The antioxidative effects of the isoflavan glabridin on endogenous constituents of LDL during its oxidation [J].
Belinky, PA ;
Aviram, M ;
Fuhrman, B ;
Rosenblat, M ;
Vaya, J .
ATHEROSCLEROSIS, 1998, 137 (01) :49-61
[3]   Structural aspects of the inhibitory effect of glabridin on LDL oxidation [J].
Belinky, PA ;
Aviram, M ;
Mahmood, S ;
Vaya, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (09) :1419-1429
[4]   The adipocyte-secreted protein Acrp30 enhances hepatic insulin action [J].
Berg, AH ;
Combs, TP ;
Du, XL ;
Brownlee, M ;
Scherer, PE .
NATURE MEDICINE, 2001, 7 (08) :947-953
[5]   Genetic vulnerability to diet-induced obesity in the C57BL/6J mouse: physiological and molecular characteristics [J].
Collins, S ;
Martin, TL ;
Surwit, RS ;
Robidoux, J .
PHYSIOLOGY & BEHAVIOR, 2004, 81 (02) :243-248
[6]   Transcript profiling suggests that differential metabolic adaptation of mice to a high fat diet is associated with changes in liver to muscle lipid fluxes [J].
de Fourmestraux, V ;
Neubauer, H ;
Poussin, C ;
Farmer, P ;
Falquet, L ;
Burcelin, R ;
Delorenzi, M ;
Thorens, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :50743-50753
[7]   Regulation of adipocytokines and insulin resistance [J].
Fasshauer, M ;
Paschke, R .
DIABETOLOGIA, 2003, 46 (12) :1594-1603
[8]  
Folin O, 1927, J BIOL CHEM, V73, P627
[9]   Licorice extract and its major polyphenol glabridin protect low-density lipoprotein against lipid peroxidation: In vitro and ex vivo studies in humans and in atherosclerotic apolipoprotein E-deficient mice [J].
Fuhrman, B ;
Buch, S ;
Vaya, J ;
Belinky, PA ;
Coleman, R ;
Hayek, T ;
Aviram, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1997, 66 (02) :267-275
[10]   Antinephritis and radical scavenging activity of prenylflavonoids [J].
Fukai, T ;
Satoh, K ;
Nomura, T ;
Sakagami, H .
FITOTERAPIA, 2003, 74 (7-8) :720-724