Treatment with oligonol, a low-molecular polyphenol derived from lychee fruit, attenuates diabetes-induced hepatic damage through regulation of oxidative stress and lipid metabolism

被引:62
作者
Noh, Jeong Sook [1 ]
Park, Chan Hum [1 ]
Yokozawa, Takako [1 ]
机构
[1] Toyama Univ, Inst Nat Med, Toyama 9300194, Japan
关键词
Oligonol; Type; 2; diabetes; Oxidative stress; Dyslipidaemia; Steatosis; GLYCATION END-PRODUCTS; INSULIN-RESISTANCE; COMPLICATIONS; ACTIVATION; MECHANISMS; GLUCOSE; BINDING; TISSUES; GLUTATHIONE; PROGRESSION;
D O I
10.1017/S0007114511001322
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
We have identified the effects of oligonol, a low-molecular polyphenol derived from lychee fruit, on oxidative stress and lipid metabolism in a type 2 diabetic model. Oligonol was orally administered at 10 or 20 mg per kg body weight per d for 8 weeks to db/db mice, and its effects were compared with those of the vehicle in db/db and m/m mice. Serum and hepatic biochemical factors, and protein and mRNA expression related to lipid metabolism were measured. In the oligonol-administered group, there were significant reductions of reactive oxygen species (ROS), lipid peroxidation, and the TAG and total cholesterol concentrations in both the serum and liver. Additionally, oligonol attenuated oxidative stress through the inhibition of advanced glycation endproduct formation and its receptor expression. Furthermore, augmented expressions of NF-kappa Bp65 and inducible NO synthase were down-regulated to the levels of m/m mice in the group treated with oligonol at 20 mg/kg. Regarding lipid metabolism, lower hepatic lipid resulted from the down-regulation of sterol regulatory element-binding protein-1 and its target gene of lipogenic enzymes in the liver of db/db mice. The present results suggest that oligonol has protective effects against ROS-related inflammation and excess lipid deposition in the type 2 diabetic liver.
引用
收藏
页码:1013 / 1022
页数:10
相关论文
共 35 条
[1]   Advanced glycation endproducts - role in pathology of diabetic complications [J].
Ahmed, N .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2005, 67 (01) :3-21
[2]  
ALI SF, 1992, NEUROTOXICOLOGY, V13, P637
[3]   Selective binding of sterol regulatory element-binding protein isoforms and co-regulatory proteins to promoters for lipid metabolic genes in liver [J].
Bennett, Mary K. ;
Datta, Young-Kyo Seo Shrimati ;
Shin, Dong-Ju ;
Osborne, Timothy F. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (23) :15628-15637
[4]   Molecular mediators of hepatic steatosis and liver injury [J].
Browning, JD ;
Horton, JD .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (02) :147-152
[5]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[6]   Free fatty acids and insulin resistance [J].
Delarue, Jacques ;
Magnan, Christophe .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2007, 10 (02) :142-148
[7]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[8]   Acute, subchronic and genotoxicity studies conducted with Oligonol, an oligomerized polyphenol formulated from lychee and green tea extracts [J].
Fujii, Hajime ;
Nishioka, Hiroshi ;
Wakame, Koji ;
Magnuson, Bernadene A. ;
Roberts, Ashley .
FOOD AND CHEMICAL TOXICOLOGY, 2008, 46 (12) :3553-3562
[9]   The role of advanced glycation end products in progression and complications of diabetes [J].
Goh, Su-Yen ;
Cooper, Mark E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (04) :1143-1152
[10]   Tea catechins and polyphenols: Health effects, metabolism, and antioxidant functions [J].
Higdon, JV ;
Frei, B .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 2003, 43 (01) :89-143