Nobiletin improves obesity and insulin resistance in high-fat diet-induced obese mice

被引:163
作者
Lee, Young-Sil [2 ]
Cha, Byung-Yoon [2 ]
Choi, Sun-Sil [2 ]
Choi, Bong-Keun [2 ]
Yonezawa, Takayuki [2 ]
Teruya, Toshiaki [3 ]
Nagai, Kazuo [1 ,2 ]
Woo, Je-Tae [1 ,2 ,4 ]
机构
[1] Chubu Univ, Dept Biol Chem, Kasugai, Aichi 4878501, Japan
[2] Chubu Univ, Res Inst Biol Funct, Kasugai, Aichi 4878501, Japan
[3] Univ Ryukyus, Fac Educ, Nishihara, Okinawa 9030213, Japan
[4] Erina Co Inc, Dept Res & Dev, Minato Ku, Tokyo 1050021, Japan
关键词
Nobiletin; High-fat diet-induced obese mice; Obesity; Insulin resistance; KAPPA-B; ADIPONECTIN; ADIPOCYTE; SENSITIVITY; ALPHA; GAMMA; DIFFERENTIATION; ANTICANCER; MOUSE;
D O I
10.1016/j.jnutbio.2012.03.014
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
Nobiletin (NOB) is a polymethoxylated flavone present in citrus fruits and has been reported to have antitumor and anti-inflammatory effects. However, little is known about the effects of NOB on obesity and insulin resistance. In this study, we examined the effects of NOB on obesity and insulin resistance, and the underlying mechanisms, in high-fat diet (HFD)-induced obese mice. Obese mice were fed a HFD for 8 weeks and then treated without (HFD control group) or with NOB at 10 or 100 mg/kg. NOB decreased body weight gain, white adipose tissue (WAT) weight and plasma triglyceride. Plasma glucose levels tended to decrease compared with the HFD group and improved plasma adiponectin levels and glucose tolerance. Furthermore, NOB altered the expression levels of several lipid metabolism-related and adipokine genes. NOB increased the mRNA expression of peroxisome proliferator-activated receptor (PPAR)-gamma, sterol regulatory element-binding protein-1c, fatty acid synthase, stearoyl-CoA desaturase-1, PPAR-alpha, carnitine palmitoyltransferase-1, uncoupling protein-2 and adiponectin, and decreased the mRNA expression of tumor necrosis factor-alpha and monocyte chemoattractant protein-1 in WAT. NOB also up-regulated glucose transporter-4 protein expression and Akt phosphorylation and suppressed I kappa B alpha degradation in WAT. Taken together, these results suggest that NOB improves adiposity, dyslipidemia, hyperglycemia and insulin resistance. These effects may be elicited by regulating the expression of lipid metabolism-related and adipokine genes, and by regulating the expression of inflammatory makers and activity of the insulin signaling pathway. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
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