Ethyl pyruvate can alleviate alcoholic liver disease through inhibiting Nrf2 signaling pathway

被引:12
作者
Shen, Fei [1 ]
Wang, Zhaohong [1 ]
Liu, Wei [2 ]
Liang, Yuji [3 ]
机构
[1] Jinan Infect Dis Hosp, Dept Liver Dis, Jinan 250000, Shandong, Peoples R China
[2] Rizhao Peoples Hosp, Dept Infect Dis, Rizhao 276800, Shandong, Peoples R China
[3] Shandong Acad Med Sci, Inst Mat Med, 22029 Jingshi Rd, Jinan 250062, Shandong, Peoples R China
关键词
ethyl pyruvate; alcoholic liver disease; Nrf2; DENSITY LIPOPROTEIN RECEPTOR; FREE FATTY-ACIDS; OXIDATIVE STRESS; INSULIN-RESISTANCE; CANCER-CELLS; MICE; INJURY; EXPRESSION; PROTEIN; INFLAMMATION;
D O I
10.3892/etm.2018.5925
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The effects of ethyl pyruvate (EP) on alcoholic liver disease and its related mechanism were investigated. Thirty male C57/BL6 mice were randomly divided to three groups: Control (n=10), alcoholic liver disease (ALD, n=10) and ethyl pyruvate group (EP, n=10). EP group was treated with gavage using EP (100 mg/kg) for 15 consecutive days. Control and ALD group were treated with the same volume of normal saline. After the last gavage, EP and ALD group were treated with the intraperitoneal injection of 50% alcoholic solution (10 ml/kg). After that, ALD and EP group received the gavage using alcohol for 4 weeks, while Control group received the same volume of normal saline, and blood and liver tissues were taken for detection. Results showed that in this experimental study that EP could effectively alleviate the alcoholic liver disease. The levels of alanine aminotransferase (AST), triglycerides (TG), free fally acid (FFA) and FBG in EP group were significantly lower than those in ALD group, but the number of platelets was reversed, and the differences were statistically significant; the levels of anti-inflammatory factors (TGE-beta/IL-10) and superoxide dismutase (SOD) in EP were significantly higher than those in ALP group, but the levels of pro-inflammatory factors (IL-6/TNF-alpha) and MDA were significantly lower than those in ALP group. EP upregulated CYP2E1, downregulated PPAR-alpha, nuclear factor 2 (Nrf2) and very-low density lipoprotein receptor (VLDLR), positively regulated the CYP2E1-PPAR-alpha-ROS signaling pathway and negatively regulated the ROS-Nrf2-VLDER signatiling pathway. EP can increase anti-inflammatory factors and decrease proinflammatory factors, enhance the activity of SOD and reduce FFA and TG. Moreover, it can upregulate the PPAR-alpha expression by negative regulation of CYP2E1-PPAR-alpha signaling pathway and downregulate the Nrf2 expression by negative regulation of Nrf2-VLDLR signaling pathway, thus alleviating the alcoholic liver disease.
引用
收藏
页码:4223 / 4228
页数:6
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