Wuxi School of Medicine, Jiangnan University, Wuxi, China.
Food Funct. 2018 Feb 21;9(2):906-916. doi: 10.1039/c7fo01051f.
Hepatic lipid accumulation and oxidative stress (OS) lead to non-alcoholic fatty liver disease (NAFLD). Thus, we hypothesized that antihyperlipidemic and antioxidant activities of niga-ichigoside F1 (NI) would ameliorate events leading to NAFLD. Lanbuzheng (Geum japonicum Thunb. var. chinense), a type of wild vegetable found in Southwest China, was used to extract NI. Male C57BL/6J mice were fed a standard diet (Con) or a high-fat diet (HFD) (denoted as diet) with or without 40 mg kg NI (defined as treatment) for 12 weeks. Diet-treatment interactions were observed in the final body weight, fat pad mass, respiratory exchange ratio (RER) in the daytime, and energy expenditure during the whole day. Moreover, NI alleviated hepatic steatosis, possibly by significantly interacting with HFD to regulate lipid metabolism genes (including Srebp1c, Acc1, Fasn, Scd1, Cpt1a and Fabp5). We also found significant diet-treatment interactions on superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT) activities, and thiobarbituric acid reactive substance (TBARS) levels, as well as the nuclear and cellular Nrf2 protein levels. Significant free fatty acid (FFA)-treatment interactions on Nrf2 nuclear translocation, antioxidant enzymes activities, genes in lipogenesis (Srebp1c, Acc1, Fasn, and Scd1), and fatty acid oxidation (Pparα) and transport (Fabp5 and Cd36) were also detected in 1 mM FFA-treated HepG2 cells with or without 20 μM NI. These beneficial effects of NI on oxidative stress and lipid accumulation were abolished by Nrf2 siRNA. Our data revealed that dietary NI could prevent HFD-induced hepatic steatosis, possibly via interacting with HFD to activate Nrf2 nuclear translocation to maintain a redox status, thus regulating lipid metabolism genes expressions.
肝脂质积累和氧化应激(OS)导致非酒精性脂肪性肝病(NAFLD)。因此,我们假设 niga-ichigoside F1(NI)的降血脂和抗氧化活性将改善导致 NAFLD 的事件。蓝布正(Geum japonicum Thunb. var. chinense)是中国西南地区的一种野生蔬菜,用于提取 NI。雄性 C57BL/6J 小鼠喂食标准饮食(Con)或高脂肪饮食(HFD)(表示为饮食),同时或不给予 40 mg kg NI(定义为治疗)12 周。在最终体重、脂肪垫质量、白天呼吸交换率(RER)和全天能量消耗方面观察到饮食-治疗相互作用。此外,NI 减轻肝脂肪变性,可能通过与 HFD 显著相互作用来调节脂质代谢基因(包括 Srebp1c、Acc1、Fasn、Scd1、Cpt1a 和 Fabp5)。我们还发现超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)、过氧化氢酶(CAT)活性和硫代巴比妥酸反应物质(TBARS)水平以及核和细胞 Nrf2 蛋白水平存在显著的饮食-治疗相互作用。在 1 mM FFA 处理的 HepG2 细胞中,也检测到 Nrf2 核易位、抗氧化酶活性、脂肪生成(Srebp1c、Acc1、Fasn 和 Scd1)和脂肪酸氧化(Pparα)和转运(Fabp5 和 Cd36)基因的显著游离脂肪酸(FFA)-治疗相互作用,同时给予或不给予 20 μM NI。NI 对氧化应激和脂质积累的这些有益作用被 Nrf2 siRNA 消除。我们的数据表明,饮食中的 NI 可以预防 HFD 诱导的肝脂肪变性,可能通过与 HFD 相互作用激活 Nrf2 核易位以维持氧化还原状态,从而调节脂质代谢基因的表达。