Pomegranate flower ameliorates fatty liver in an animal model of type 2 diabetes and obesity

被引:123
作者
Xu, Kevin Zhe-Yang [1 ]
Zhu, Chenchen [2 ]
Kim, Moon Sun [1 ]
Yamahara, Johji [3 ]
Li, Yuhao [1 ]
机构
[1] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
[2] Guangzhou Univ Chinese Med, Sch Pharm, Guangzhou, Peoples R China
[3] Pharmafood Inst, Kyoto, Japan
关键词
Pomegranate; Diabetes; Liver; Lipid metabolism; Peroxisome proliferator-activated receptor; ACTIVATED-RECEPTOR-ALPHA; STEAROYL-COA DESATURASE-1; CARDIAC LIPID-METABOLISM; NONALCOHOLIC STEATOHEPATITIS; SKELETAL-MUSCLE; OLEANOLIC ACID; ADIPOSE-TISSUE; INSULIN ACTION; PROTECTS MICE; URSOLIC ACID;
D O I
10.1016/j.jep.2009.03.035
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Aims of the study: Fatty liver is the most common cause of abnormal liver function tests. We investigated the effect and its underlying mechanism of pomegranate flower (PGF), a traditional antidiabetic medicine, on fatty liver. Materials and methods: At the endpoint of treatment of male Zucker diabetic fatty (ZDF) rats with PGF extract (500 mg/kg, p.o. x 6 weeks), liver weight index, hepatic lipid contents (enzymatic colorimetric methods) and droplet accumulation (Oil Red 0 staining) were determined. Gene profiles (RT-PCR) were analyzed in the liver of ZDF rats and in human liver-derived HepG2 cell line. Results: PGF-treated ZDF rats showed reduced ratio of liver weight to tibia length, hepatic triglyceride contents and lipid droplets. These effects were accompanied by enhanced hepatic gene expression of peroxisome proliferator-activated receptor (PPAR)-alpha, carnitine palmitoyltransferase-1 and acyl-CoA oxidase (ACO), and reduced stearoyl-CoA desaturase-1. In contrast, PGF showed minimal effects on expression of genes responsible for synthesis, hydrolysis or uptake of fatty acid and triglycerides. PGF treatment also increased PPAR-alpha and ACO mRNA levels in HepG2 cells. Conclusion: Our findings suggest that this Unani medicine ameliorates diabetes and obesity-associated fatty liver, at least in part, by activating hepatic expression of genes responsible for fatty acid oxidation. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:280 / 287
页数:8
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