Schizandrin A supplementation improves nonalcoholic fatty liver disease in mice fed a high-fat and high-cholesterol diet

被引:23
|
作者
Jeong, Mi Ji [1 ]
Kim, Sang Ryong [2 ]
Jung, Un Ju [1 ]
机构
[1] Pukyong Natl Univ, Dept Food Sci & Nutr, 45 Yongso Ro, Busan 48513, South Korea
[2] Kyungpook Natl Univ, Sch Life Sci, BK21 Plus KNU Creat BioRes Grp, 1370 San Kyuk Dong, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
Schizandrin A; Nonalcohol fatty liver disease; Lipid metabolism; Antioxidant activity; High-fat and high-cholesterol diet; OXIDATIVE STRESS; METABOLIC SYNDROME; ACID HOMEOSTASIS; GENE-EXPRESSION; ABCA1; INHIBITION; CHINENSIS; ASSAY; 7-ALPHA-HYDROXYLASE; PATHOGENESIS;
D O I
10.1016/j.nutres.2019.01.001
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
We hypothesized that schizandrin (SCH) A, a lignan found in the fruits of the Schisandra genus, would exert protective effects against high-fat and high-cholesterol (HFHC) diet-induced nonalcoholic fatty liver disease (NAFLD) via regulation of lipid metabolism and oxidative stress. To test our hypothesis, male C57BL/6J mice were fed an HFHC diet with or without SCH A for 15 weeks. There were no significant differences in food intake, body weight, fat mass, and plasma total cholesterol level between the 2 groups. However, supplementation of SCH A significantly decreased levels of plasma free fatty acid and triglyceride, whereas plasma high-density lipoprotein cholesterol level was increased in the SCH A-supplemented mice. Moreover, hepatic free fatty acid, triglyceride, and cholesterol content, as well as hepatic lipid droplet accumulation, were markedly lower in the SCH A group in contrast to the control group. Activity of hepatic enzymes involved in fatty acid and triglyceride synthesis was significantly decreased by SCH A supplementation, whereas SCH A markedly increased hepatic beta-oxidation and fatty acid oxidation-related gene expression as well as fecal excretion of free fatty acid and triglyceride. SCH A also significantly increased expression of genes involved in cholesterol homeostasis (biliary cholesterol excretion and cholesterol efflux to high-density lipoprotein) in the liver. Moreover, SCH A significantly decreased hepatic lipid peroxidation, which was accompanied by increased hepatic antioxidant enzymes activity. These results suggest that SCH A could alleviate HFHC diet-induced NAFLD by regulating hepatic lipid metabolism and oxidative stress as well as fecal lipid excretion. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:64 / 71
页数:8
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