Hwang Jin-Taek, Shin Eun Ju, Chung Min-Yu, Park Jae Ho, Chung Sangwon, Choi Hyo-Kyoung
Korea Food Research Institute, 245 Nongsaengmyeong-ro, Jeonbuk 55365, Korea.
Department of Food Biotechnology, Korea University of Science & Technology, Daejeon 34113, Korea.
Nutr Res Pract. 2018 Apr;12(2):110-117. doi: 10.4162/nrp.2018.12.2.110. Epub 2018 Mar 22.
BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease and is closely associated with metabolic syndrome. In the present study, we observed the effect of ethanol extract of (EAF) on NAFLD and have suggested the possibility of using EAF as a natural product for application in the development of a treatment for NAFLD.
MATERIALS/METHODS: The preventive effect on hepatic lipid accumulation was estimated by using an oleic acid (OA)-induced NAFLD model and a Western diet (high-fat high-sucrose; WD)-induced obese mouse model. Animals were divided into three groups (n = 7): normal diet group (ND), WD group, and WD plus 1% EAF group.
EAF reduced OA-stimulated lipid accumulation in HepG2 cells in the absence of cellular cytotoxicity and significantly blocked transcriptional activation of sterol regulatory element-binding protein 1 and fatty acid synthase genes. Subsequently, we investigated these effects in mice fed either ND or WD in the presence or absence of EAF supplementation. In comparison to the ND controls, the WD-fed mice exhibited increases in body weight, liver weight, epididymal fat weight, and accumulation of fat in hepatocytes, and these effects were significantly attenuated by EAF supplementation.
attenuates the development of NAFLD, and EAF elicits anti-lipogenic activity in liver. Therefore, EAF represents a promising candidate for use in the development of novel therapeutic drugs or drug combinations for the prevention and treatment of NAFLD.
背景/目的:非酒精性脂肪性肝病(NAFLD)是慢性肝病的主要病因,与代谢综合征密切相关。在本研究中,我们观察了[具体植物名称]乙醇提取物(EAF)对NAFLD的影响,并提出了将EAF作为天然产物用于开发NAFLD治疗方法的可能性。
材料/方法:通过油酸(OA)诱导的NAFLD模型和西方饮食(高脂肪高蔗糖;WD)诱导的肥胖小鼠模型评估对肝脏脂质积累的预防作用。将动物分为三组(n = 7):正常饮食组(ND)、WD组和WD加1% EAF组。
EAF在无细胞毒性的情况下减少了HepG2细胞中OA刺激的脂质积累,并显著阻断了固醇调节元件结合蛋白1和脂肪酸合酶基因的转录激活。随后,我们在补充或不补充EAF的情况下,对喂食ND或WD的小鼠研究了这些作用。与ND对照组相比,喂食WD的小鼠体重、肝脏重量、附睾脂肪重量增加,肝细胞中脂肪积累增加,而补充EAF可显著减轻这些作用。
[具体植物名称]可减轻NAFLD的发展,EAF在肝脏中具有抗脂肪生成活性。因此,EAF是开发用于预防和治疗NAFLD的新型治疗药物或药物组合的有希望的候选物。