Journal of Capital Medical University ›› 2017, Vol. 38 ›› Issue (2): 268-276.doi: 10.3969/j.issn.1006-7795.2017.02.021

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Effect of epalrestat on liver injury in type 2 diabetic rats

Zhao Yuerong1,2, Hou Biyu2, Liu Chenge2, Wang Xiaobo1,2, Du Guanhua2, Zhang Li2, Guan Shuyu1   

  1. 1. School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China;
    2. Beijing Key Laboratory of Drug Target Research and Drug Screening, Institute of Materia Medica, Chinese Academy of Medical Sciences, Beijing 100050, China
  • Received:2016-12-15 Online:2017-03-21 Published:2017-04-17
  • Supported by:
    This study was supported by National Science and Technology Major Projects for “Major New Drugs Innovation and Development” (2013ZX09508104)

Abstract: Objective This study investigated the effect of epalrestat on liver injury in rats with type 2 diabetic mellitus (T2DM). Methods SD rats were fed with high-fat and high-sucrose diet for four weeks, then 45 mg·kg-1 Streptozotocin (STZ) was injected intraperitoneally to make the animal model of type 2 diabetes. Diabetic rats were divided into two groups as the model group and the epalrestat group (100 mg·kg-1), another 12 normal SD rats were served as the control group. The diabetic rats were treated with or without epalrestat by gavaging for 8 weeks. Body weight, food and water intake, blood glucose level, blood lipids were measured; liver function, liver pathological changes and oxidative stress were examined. Immunohistochemistry of α-smooth muscle actin (α-SMA)and transforming growth factor-β1 (TGF-β1) were conducted. Results Compared with the model group, epalrestat could reduce the concentration of fasting plasma glucose and blood lipids. The index for liver condition and oxidative stress were down regulated. Pathological examination showed that lesions of hepatic inflammation and fibrosis were significantly alleviated. The expressions of α-SMA and TGF-β1 were markedly reduced in liver tissues of type 2 diabetic rats with the treatment of epalrestat. Conclusion Epalrestat could alleviate liver inflammation and hepatic fibrosis of rats with T2DM via anti-oxidative stress and inhibiting the activation of hepatic stellate cell.

Key words: epalrestat, type 2 diabetic mellitus, oxidative stress, hepatic fibrosis

CLC Number: