Department of Life Science, Gachon University, Sungnam, Gyeonggido 13120, Korea.
Department of Food Science and Biotechnology, Sejong University, Seoul 05006, Korea.
Nutrients. 2019 May 6;11(5):1015. doi: 10.3390/nu11051015.
Nonalcoholic fatty liver diseases (NAFLD) is characterized by accumulation of lipid droplets in the liver. The objective of this study was to evaluate protective effects of fermented extract by ON188 (ONE) against hepatosteatosis and obesity in mice fed a high-fat diet (HFD). Eight-week-old male C57BL/6J mice were fed HFD mixed with ONE for four weeks and its effects on hepatosteatosis and obesity were examined. Although ONE did not change food intake, it reduced body weights of mice at administration dose of 200 mg/kg/day. Activities of lactate dehydrogenase (LDH), aspartate transaminase (AST), and alanine transaminase (ALT) as plasma parameters were reduced by ONE in a dose-dependent manner. Hepatic lipid droplets and triglyceride (TG) levels were also reduced by ONE due to upregulation of fatty acid oxidizing genes such as carnithine palmitoyltransferase (CPT1) and peroxisomal proliferator activated receptor α(PPARα) mediated by induction of sphingosine kinase 2 (SPHK2). In epididymal fat tissue, sizes of adipocytes were significantly reduced by ONE in a dose-dependent manner. This is mainly due to suppression of lipogenesis and upregulation of adipocyte browning genes. Collectively, these results suggest that fermented ONE can activate fatty acid oxidation via SPHK2 in the liver. It can also suppress lipogenesis and activate browning in adipose tissue. Thus, ONE might have potential to be used for the development of functional foods against liver dysfunction and obesity.
非酒精性脂肪性肝病 (NAFLD) 的特征是肝脏中脂肪滴的积累。本研究的目的是评估发酵提取物 ON188 (ONE) 对高脂肪饮食 (HFD) 喂养小鼠肝脂肪变性和肥胖的保护作用。将 8 周龄雄性 C57BL/6J 小鼠用 HFD 与 ONE 混合喂养 4 周,并检查其对肝脂肪变性和肥胖的影响。虽然 ONE 没有改变食物摄入量,但它降低了 200mg/kg/天给药剂量的小鼠体重。乳酸脱氢酶 (LDH)、天冬氨酸转氨酶 (AST) 和丙氨酸转氨酶 (ALT) 的活性作为血浆参数,呈剂量依赖性降低。肝脂肪滴和甘油三酯 (TG) 水平也因 ONE 上调脂肪酸氧化基因,如肉碱棕榈酰转移酶 (CPT1) 和过氧化物酶体增殖物激活受体α (PPARα),而降低,这是通过诱导鞘氨醇激酶 2 (SPHK2) 介导的。在附睾脂肪组织中,脂肪细胞的大小也因 ONE 呈剂量依赖性显著减小。这主要是由于脂肪生成受到抑制和脂肪细胞褐变基因的上调。总之,这些结果表明,发酵的 ONE 可以通过 SPHK2 在肝脏中激活脂肪酸氧化。它还可以抑制脂肪生成并激活脂肪组织中的褐变。因此,ONE 可能具有作为开发功能性食品以对抗肝功能障碍和肥胖的潜力。