Citrus unshiu peel extract ameliorates hyperglycemia and hepatic steatosis by altering inflammation and hepatic glucose- and lipid-regulating enzymes in db/db mice

被引:79
|
作者
Park, Hae-Jin [1 ,2 ]
Jung, Un Ju [1 ,2 ]
Cho, Su-Jung [1 ,2 ]
Jung, Hee-Kyung [3 ]
Shim, Sangphil [4 ]
Choi, Myung-Sook [1 ,2 ]
机构
[1] Kyungpook Natl Univ, Dept Food Sci & Nutr, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Ctr Food & Nutr Genom Res, Taegu 702701, South Korea
[3] Bio Ind Ctr, Taegu, South Korea
[4] Foodwell Corp, Taegu, South Korea
来源
JOURNAL OF NUTRITIONAL BIOCHEMISTRY | 2013年 / 24卷 / 02期
基金
新加坡国家研究基金会;
关键词
Citrus unshiu peel extract; Type 2 diabetic db/db mice; Anti-diabetic; Lipid metabolism; Inflammation; FATTY LIVER-DISEASE; PHOSPHOENOLPYRUVATE CARBOXYKINASE GTP; DEPENDENT DIABETES-MELLITUS; INSULIN-RESISTANCE; METABOLIC SYNDROME; C57BL/KSJ-DB/DB MICE; TRANSGENIC MICE; OBESE MICE; ROSIGLITAZONE; ADIPONECTIN;
D O I
10.1016/j.jnutbio.2011.12.009
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
Insulin resistance in Type 2 diabetes leads to hepatic steatosis that can accompanied by progressive inflammation of the liver. Citrus unshiu peel is a rich source of citrus flavonoids that possess anti-inflammatory, anti-diabetic and lipid-lowering effects. However, the ability of citrus unshiu peel ethanol extract (CPE) to improve hyperglycemia, adiposity and hepatic steatosis in Type 2 diabetes is unknown. Thus, we evaluated the effects of CPE on markers for glucose, lipid metabolism and inflammation in Type 2 diabetic mice. Male C57BL/KsJ-db/db mice were fed a normal diet with CPE (2 g/100 g diet) or rosiglitazone (0.001 g/100 g diet) for 6 weeks. Mice supplemented with the CPE showed a significant decrease in body weight gain, body fat mass and blood glucose level. The antihyperglycemic effect of CPE appeared to be partially mediated through the inhibition of hepatic gluconeogenic phosphoenolpyruvate carboxykinase mRNA expression and its activity and through the induction of insulin/glucagon secretion. CPE also ameliorated hepatic steatosis and hypertriglyceridemia via the inhibition of gene expression and activities of the lipogenic enzymes and the activation of fatty acid oxidation in the liver. These beneficial effects of CPE may be related to increased levels of anti-inflammatory adiponectin and interleukin (IL)-10, and decreased levels of pro-inflammatory markers (IL-6, monocyte chemotactic protein-1, interferon-gamma and tumor necrosis factor-alpha) in the plasma or liver. Taken together, we suggest that CPE has the potential to improve both hyperglycemia and hepatic steatosis in Type 2 diabetes. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:419 / 427
页数:9
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