Department of Food Science and Nutrition, Pukyong National University, 45 Yongso-ro, Nam-gu, Busan 48513, Republic of Korea.
School of Life Sciences, BK21 plus KNU Creative BioResearch Group, Kyungpook National University, 1370 San-Kyuk Dong, Puk-Ku, Daegu 41566, Republic of Korea.
Nutr Res. 2019 Apr;64:64-71. doi: 10.1016/j.nutres.2019.01.001. Epub 2019 Jan 11.
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 β-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.
我们假设五味子甲素(SCH)A,一种在五味子属果实中发现的木脂素,将通过调节脂质代谢和氧化应激对高脂肪和高胆固醇(HFHC)饮食诱导的非酒精性脂肪肝(NAFLD)发挥保护作用。为了验证我们的假设,雄性 C57BL/6J 小鼠用 HFHC 饮食或 HFHC 饮食加 SCH A 喂养 15 周。两组间的食物摄入量、体重、脂肪量和血浆总胆固醇水平没有显著差异。然而,SCH A 的补充显著降低了血浆游离脂肪酸和甘油三酯水平,而高脂饲料加 SCH A 的小鼠的血浆高密度脂蛋白胆固醇水平升高。此外,与对照组相比,SCH A 组的肝脏游离脂肪酸、甘油三酯和胆固醇含量以及肝内脂质滴积累明显降低。SCH A 补充显著降低了参与脂肪酸和甘油三酯合成的肝酶活性,而 SCH A 显著增加了肝脏β-氧化和脂肪酸氧化相关基因的表达以及游离脂肪酸和甘油三酯的粪便排泄。SCH A 还显著增加了肝脏胆固醇稳态(胆汁胆固醇排泄和胆固醇向高密度脂蛋白的流出)相关基因的表达。此外,SCH A 显著降低了肝脏脂质过氧化,同时增加了肝脏抗氧化酶的活性。这些结果表明,SCH A 可以通过调节肝脏脂质代谢和氧化应激以及粪便脂质排泄来减轻 HFHC 饮食诱导的 NAFLD。