Curcumin analog CUR5-8 ameliorates nonalcoholic fatty liver disease in mice with high-fat diet-induced obesity

被引:74
作者
Lee, Eun Soo [1 ]
Kwon, Mi-Hye [2 ]
Kim, Hong Min [1 ]
Woo, Ho Bum [3 ]
Ahn, Chan Mug [3 ]
Chung, Choon Hee [1 ]
机构
[1] Yonsei Univ, Dept Internal Med, Wonju Coll Med, Wonju 220701, South Korea
[2] Gangneung Wonju Natl Univ, East Coast Res Inst Life Sci, Kangnung, South Korea
[3] Yonsei Univ, Dept Basic Sci, Wonju Coll Med, Wonju 220701, South Korea
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2020年 / 103卷
基金
新加坡国家研究基金会;
关键词
Autophagy; Curcumin; Diabetes; Nonalcoholic fatty liver disease; Lipid metabolism; INSULIN-RESISTANCE; AUTOPHAGY; ANTIOXIDANT; APOPTOSIS; ACTIVATION; GAMMA;
D O I
10.1016/j.metabol.2019.154015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Nonalcoholic fatty liver disease (NAFLD) occurs when excess fat storage in the liver and it is strongly linked with metabolic syndrome including obesity, insulin resistance, dyslipidemia and hypertension. Curcumin5-8 (CUR5-8) is a synthetic derivative of naturally active curcumin (CUR) that has anti-oxidative and anti-inflammatory properties. In the present study, we investigated the effects of CUR5-8, a novel CUR analog, on hepatic steatosis in mice with high-fat diet (HFD)-induced obesity. Methods: Based on their diets for 13 weeks, the mice were categorized into the following six groups: regular diet (RD, n = 10), RD with CUR (RD + CUR, 100 mg/kg/day, n = 10), RD with CUR5-8 (RD + CUR5-8, 100 mg/kg/day, n = 10), high-fat diet-induced obese mice (HFD, n = 10), HFD with CUR (HFD + CUR, 100 mg/kg/day, n = 10), and HFD with CUR5-8 (HFD + CUR5-8, 100 mg/kg/day, n = 10) for 13 weeks. Hematoxylin and eosin (H&E) staining of the sections revealed hepatic steatosis. Results: CUR5-8 administration prevented increase in body and liver weights in mice with HFD-induced obesity. Compared to the HFD group, insulin resistance was significantly improved in the HFD + CUR5-8 group. Serum alanine aminotransferase level, which is an indicator of liver damage, was also decreased after CUR5-8 administration. H&E staining revealed that CUR5-8 treatment decreased hepatic steatosis in mice with HFD-induced obesity. Interestingly, CUR5-8, and not CUR, decreased the elevated liver triglyceride level induced by the HFD. Conclusions: These findings suggest that CUR5-8 ameliorates insulin resistance and hepatic steatosis in mice with HFD-induced obesity. (C) 2019 The Authors. Published by Elsevier Inc.
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页数:9
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