Cassia tora (Leguminosae) seed extract alleviates high-fat diet-induced nonalcoholic fatty liver

被引:23
作者
Tzeng, Thing-Fong [1 ]
Lu, Hung-Jen [2 ]
Liou, Shorong-Shii [3 ,4 ]
Chang, Chia Ju [5 ]
Liu, I-Min [3 ,4 ]
机构
[1] Pao Chien Hosp, Dept Internal Med, Ping Tung City, Pingtung County, Taiwan
[2] Kaohsiung Vet Gen Hosp, Tradit Med Ctr, Kaohsiung, Taiwan
[3] Tajen Univ, Dept Pharm, Yanpu Shiang, Ping Tung Shien, Taiwan
[4] Tajen Univ, Grad Inst Pharmaceut Technol, Yanpu Shiang, Ping Tung Shien, Taiwan
[5] China Med Univ, Sch Chinese Pharmaceut Sci & Chinese Med Resource, Taichung, Taiwan
关键词
Cassia tora seeds; High-fat diet; AMP-activated protein kinase; Fatty liver; DENSITY-LIPOPROTEIN CHOLESTEROL; INHIBITORY-ACTIVITY; ANTHRAQUINONES; INSULIN; AMPK; STEATOHEPATITIS; METABOLISM; GLYCATION; DISEASE; PLASMA;
D O I
10.1016/j.fct.2012.09.024
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The aim of this study was to examine the effects of Cassia tora seeds on high-fat diet (HFD)-induced hepatic steatosis, and elucidate the molecular mechanisms behind its effects. After being fed a HFD for two weeks, rats were orally dosed with Cassia seed ethanol extract (CSEE) (100, 200, or 300 mg/kg) once daily for 8 weeks. CSEE induced dose-dependent reductions in plasma lipid levels, as well as decreased the over hepatic lipid accumulation. Furthermore, CSEE treatment improved HFD-induced hepatic histological lesions. CSEE enhanced the phosphorylation of AMP-activated protein kinase (AMPK) and its primary downstream targeting enzyme, acetyl-CoA carboxylase, up-regulated the gene expression of carnitine palmitoyl transferase 1, and down-regulated sterol regulatory element binding protein 1 and fatty acid synthase protein levels in the livers of HFD-fed rats. AMPK inhibition by compound C retarded CSEE-induced reduction in triglyceride accumulation in HepG2 cells stimulated by insulin. Our findings suggest that CSEE may regulate hepatic lipid homeostasis related with an AMPK-dependent signaling pathway. Targeting AMPK activation with CSEE may represent a promising approach for the prevention and treatment of obesity-related non-alcoholic fatty liver disease. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:194 / 201
页数:8
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