Xie Tian-Hong, Li Jun-Xiang, Mao Tang-You, Guo Yi, Chen Chen, Han Ya-Fei, Tan Xiang, Chen Run-Hua
Beijing University of Chinese Medicine, No. 11, North Third Ring East Road, Beijing 100029, China.
Gastroenterology Department, Dongfang Hospital, Beijing University of Chinese Medicine, No. 6, 1st Section, Fangxingyuan, Fangzhuang, Beijing 100078, China.
Evid Based Complement Alternat Med. 2017;2017:4603701. doi: 10.1155/2017/4603701. Epub 2017 Jun 7.
ErChen and YinChen decoction (ECYCD) is an effective traditional Chinese medicine and has been widely used in traditional Chinese medicine to treat nonalcoholic steatohepatitis (NASH), with good curative effects. However, the specific mechanisms underlying these effects are unclear. In this study, we determined the efficacy of ECYCD in a high-fat diet-induced NASH rat model, established by 8-week administration of a high-fat diet. ECYCD was administered daily for 4 weeks, after which the rats were euthanized. The results demonstrated that ECYCD ameliorated high-fat diet-induced NASH, as evidenced by decreased liver indexes, reduced hepatic lipid deposition and liver injury, lower serum biochemistry markers (including low-density lipoprotein), and reduced HOMA-IR scores. Moreover, levels of free fatty acids, tumor necrosis factor, and malondialdehyde were decreased, whereas glutathione was increased in the liver. Serum high-density lipoprotein was also increased in the liver, and ECYCD regulated the c-Jun N-terminal kinase 1 (JNK1) signaling pathway by decreasing the levels of JNK1 protein, mRNA, activator protein- (AP-) 1 protein, mRNA, and phospho-insulin receptor substrate- (IRS-) 1 and increasing phopsho-PKB levels. These results suggested that ECYCD could ameliorate high-fat diet-induced NASH in rats through JNK1 signaling. ECYCD may be a safe therapeutic option for the treatment of NASH.
二陈茵陈汤(ECYCD)是一种有效的中药,在中医领域已被广泛用于治疗非酒精性脂肪性肝炎(NASH),疗效良好。然而,这些作用的具体机制尚不清楚。在本研究中,我们在通过8周高脂饮食建立的高脂饮食诱导的NASH大鼠模型中确定了ECYCD的疗效。ECYCD每日给药4周,之后对大鼠实施安乐死。结果表明,ECYCD改善了高脂饮食诱导的NASH,表现为肝脏指数降低、肝脏脂质沉积和肝损伤减轻、血清生化标志物(包括低密度脂蛋白)降低以及HOMA-IR评分降低。此外,肝脏中游离脂肪酸、肿瘤坏死因子和丙二醛水平降低,而谷胱甘肽增加。肝脏中血清高密度脂蛋白也增加,并且ECYCD通过降低JNK1蛋白、mRNA、活化蛋白-(AP-)1蛋白、mRNA以及磷酸化胰岛素受体底物-(IRS-)1的水平并增加磷酸化蛋白激酶B(PKB)水平来调节c-Jun氨基末端激酶1(JNK1)信号通路。这些结果表明,ECYCD可通过JNK1信号通路改善高脂饮食诱导的大鼠NASH。ECYCD可能是治疗NASH的一种安全的治疗选择。