实用肝脏病杂志 ›› 2020, Vol. 23 ›› Issue (2): 163-166.doi: 10.3969/j.issn.1672-5069.2020.02.004

• 实验性肝炎 • 上一篇    下一篇

非酒精性脂肪性肝病小鼠肝组织与脂质代谢相关基因FAS、ACC和SREBP-1水平分析*

张猛, 陈晹, 刘娇, 李叶晟, 黄杨卿   

  1. 201508 上海市 复旦大学附属上海市公共卫生临床中心肝胆外科
  • 收稿日期:2019-04-19 出版日期:2020-03-10 发布日期:2020-04-20
  • 通讯作者: 黄杨卿,E-mail:eric_huangyq@163.com
  • 作者简介:张猛,男,29岁,医学硕士,主治医师。主要从事肝脏疾病诊断与治疗学研究。E-mail:zhangmeng152569@126.com
  • 基金资助:
    上海市卫生和计划生育委员会科研项目(编号:201840128)

Up-regulation of lipid metabolism related genes in liver tissues of mice with nonalcoholic fatty liver diseases

Zhang Meng, Chen Yi, Liu Jiao, et al   

  1. Department of Hepatobiliary Surgery , Public Health Clinical Center, Fudan University , Shanghai 201508, China
  • Received:2019-04-19 Online:2020-03-10 Published:2020-04-20

摘要: 目的 探讨非酒精性脂肪性肝病(NAFLD)小鼠肝组织脂质代谢相关基因水平变化。方法 采用高脂饲料喂养20小鼠,构建小鼠NAFLD动物模型,观察小鼠肝组织病理学变化,检测血清总胆固醇(TCH) 和甘油三酯(TG)含量,采用RT-PCR法检测小鼠肝组织胆固醇调节元件结合蛋白(SREBPs)、乙酰辅酶A羧化酶(ACC)和脂肪酸合成酶(fatty acid synthase, FAS)基因变化。结果 10只NAFLD模型小鼠肝细胞排列不整齐,肝细胞内出现大小不等的脂滴;NAFLD模型小鼠血清TG和TCH水平分别为(0.63±0.13)mmol/L和(7.23±0.7)mmol/L,显著高于10只对照组[(0.28±0.06)mmol/L和(2.78±0.6)mmol/L,P<0.001];在实验24 w末,NAFLD组小鼠肝组织FAS 和SREBP-1 mRNA水平分别为(3.9±1.1)和(1.8±0.7),对照组则分别为【(1.0±0.3)和(1.0±0.4),FAS: t = 6.231, P<0.001; SREBP-1: t =2.431, P =0.035】,差异显著,而NAFLD组小鼠肝组织ACC mRNA水平为(1.2±0.5),与对照组【(1.0±0.4), t=0.765, P=0.462】比,无显著差异。结论 NAFLD模型小鼠肝组织与脂质代谢相关基因显著上调,为进一步研究NAFLD的发生发展机制奠定了基础。

关键词: 非酒精性脂肪性肝病, 脂质代谢, 脂肪酸合成酶, 胆固醇调节元件结合蛋白, 小鼠

Abstract: Objective The aim of this experiment was to investigate the changes of lipid metabolism related genes in liver tissues of mice with nonalcoholic fatty liver diseases (NAFLD). Methods A NAFLD model was established in ten mice by feeding high-fat diet. The histopathological changes of the liver tissues were observed. Blood total cholesterol (TCH) and triglycerides (TG) levels were detected, and sterol regulatory element-binding proteins (SREBPs), acetyl coenzyme carboxylase (ACC) and fatty acid synthase (FAS) mRNA were detected by reverse transcription-polymerase chain reaction. Results The steatosis of liver cells was found in mice in NAFLD model group; blood TG and TCH levels in NAFLD model group were (0.63±0.13) mmol/L and (7.23±0.7) mmol/L, significantly higher than [(0.28± 0.06) mmol/L and (2.78±0.6) mmol/L, P<0.001] in ten mice in the control; at the end of 24 w experiment, hepatic FAS and SREBP-1 mRNA in NAFLD mice were (3.9±1.1) and (1.8±0.7), significantly higher than 【(1.0±0.3) and (1.0±0.4), FAS: t = 6.231, P<0.001; SREBP-1: t = 2.431, P =0.035】, while the ACC mRNA was (1.2±0.5), not significantly different as compared to 【(1.0±0.4), t = 0.765, P =0.462】 in the control. Conclusion The lipid metabolism related genes in liver tissue of mice with NAFLD are significantly up-regulated, which might play a pivotal role in the pathogenesis of NAFLD.

Key words: Nonalcoholic fatty liver, Lipid metabolism, Sterol regulatory element-binding proteins, Acetyl coenzyme carboxylase, Fatty acid synthase, Mice