Jeong Hyeneui, Kim Jong-Won, Yang Myeon-Sik, Park Chul, Kim Jong Hoon, Lim Chae Woong, Kim Bumseok
1 Biosafety Research Institute and Laboratory of Pathology, (BK21 Plus Program), College of Veterinary Medicine, Chonbuk National University, Iksan, Republic of Korea.
Am J Chin Med. 2018 Oct 9:1-27. doi: 10.1142/S0192415X18500817.
Korean red ginseng (KRG) is a traditional herbal medicine used to prevent several geriatric diseases due to its therapeutic effects on metabolic disorder, including type 2 diabetes and fatty liver disease. In this study, we investigated the effects of KRG on the progression of nonalcoholic steatohepatitis (NASH) in mice. NASH was induced by feeding a methionine- and choline-deficient high-fat or high-fat/high-sucrose diet for 6 or 13 weeks, respectively. Each diet group was also orally administered saline (group G0) or KRG extract (100, 200, or 400 mg/kg/day; groups G1, G2, and G4, respectively). KRG showed anti-inflammatory and antifibrogenic effects in the diet-induced NASH models. Furthermore, the expression levels of lipid metabolism-related genes were markedly decreased with KRG treatment in both diet-induced NASH groups. We next confirmed the expression levels of FABP4 in the liver and its ability to regulate inflammation and/or oxidative stress. We observed decreased levels of FABP4 mRNA and protein in the KRG-treated groups indicating that KRG affects the pathogenesis of NASH-related inflammatory responses by modulating FABP4 expression. Results of in vitro experiments showed similar patterns in cells treated with KRG, indicating that KRG treatment regulates the expression of FABP4 and subsequently reduces NASH related inflammation. Our findings suggest a novel role of KRG in NASH-related inflammatory responses via modulation of FABP4 expression in the liver. KRG may be a safe alternative therapy to prevent NASH progression.
韩国红参(KRG)是一种传统草药,因其对包括2型糖尿病和脂肪肝疾病在内的代谢紊乱具有治疗作用,可用于预防多种老年疾病。在本研究中,我们研究了KRG对小鼠非酒精性脂肪性肝炎(NASH)进展的影响。分别通过喂食蛋氨酸和胆碱缺乏的高脂肪或高脂肪/高糖饮食6周或13周来诱导NASH。每个饮食组还口服生理盐水(G0组)或KRG提取物(分别为100、200或400mg/kg/天;G1、G2和G4组)。KRG在饮食诱导的NASH模型中显示出抗炎和抗纤维化作用。此外,在两个饮食诱导的NASH组中,KRG处理后脂质代谢相关基因的表达水平均显著降低。接下来,我们证实了肝脏中脂肪酸结合蛋白4(FABP4)的表达水平及其调节炎症和/或氧化应激的能力。我们观察到KRG处理组中FABP4 mRNA和蛋白水平降低,表明KRG通过调节FABP4表达影响NASH相关炎症反应的发病机制。体外实验结果显示,用KRG处理的细胞呈现相似模式,表明KRG处理可调节FABP4的表达,进而减轻NASH相关炎症。我们的研究结果表明,KRG通过调节肝脏中FABP4的表达在NASH相关炎症反应中发挥新作用。KRG可能是预防NASH进展的一种安全替代疗法。