基础医学与临床 ›› 2024, Vol. 44 ›› Issue (5): 699-704.doi: 10.16352/j.issn.1001-6325.2024.05.0699

• 研究论文 • 上一篇    下一篇

肥胖模型小鼠肝脏的病理变化及代谢组分析

丁宝锋, 王小爽, 王芳, 余佳*   

  1. 中国医学科学院基础医学研究所 北京协和医学院基础学院 重大疾病共性机制研究全国重点实验室,北京 100005
  • 收稿日期:2024-02-26 修回日期:2024-03-19 出版日期:2024-05-05 发布日期:2024-04-23
  • 通讯作者: *j-yu@ibms.pumc.edu.cn
  • 基金资助:
    国家重点研发计划(2019YFA0801800)

Pathological changes and metabolome analysis of liver in obese mouse models

DING Baofeng, WANG Xiaoshuang, WANG Fang, YU Jia*   

  1. State Key Laboratory of Common Mechanism Research for Major Diseases,Institute of Basic Medical Sciences CAMS, School of Basic Medicine PUMC,Beijing 100005,China
  • Received:2024-02-26 Revised:2024-03-19 Online:2024-05-05 Published:2024-04-23
  • Contact: *j-yu@ibms.pumc.edu.cn

摘要: 目的 检测肥胖模型小鼠的肝脏病理变化,并探究肥胖对肝脏代谢的影响。方法 通过24周的持续高脂饮食(HFD)喂养,建立肥胖模型小鼠,对照组为正常饮食(CD)喂养。24周后,解剖观察肝脏病变,利用苏木精-伊红(HE)染色和天狼猩红染色观察肝脏组织病理特点。取适量肝脏组织于80%甲醇中萃取后,利用超高效液相色谱-质谱(UPLC-MS)进行代谢组检测;并对所获得的代谢组数据进行主成分分析(PCA)、差异代谢物分析以及KEGG通路富集分析,探究肥胖小鼠肝脏的代谢改变。结果 高脂饮食24周后,HFD组小鼠的体质量和肝脏质量均显著高于正常饮食的CD组;HFD组小鼠肝脏脂肪变性程度严重,出现轻微纤维化;两组小鼠肝脏代谢物具有明显差异,且HFD组小鼠肝脏的代谢改变主要集中在苯丙氨酸代谢、柠檬酸循环(TCA循环)、鞘脂类代谢、精氨酸生物合成、初级胆汁酸的生物合成等代谢通路。结论 成功构建肥胖模型小鼠,阐明了肥胖小鼠肝脏的病理特征;对肥胖小鼠肝脏进行代谢组学分析,揭示了肥胖小鼠肝脏的主要代谢通路改变。

关键词: 肥胖, 肝脏, 代谢组, 饮食诱导

Abstract: Objective To detect the pathological changes in obese mice liver and explore the effects of obesity on hepatic metabolism. Methods Obese mouse model was successfully constructed by consecutive 24 weeks of high fat diet (HFD), while control group was fed with a standard chow diet (CD). After 24 weeks, mice liver was dissected, and the pathological characteristics of liver were observed with hematoxylin-eosin (HE) staining and Sirius red staining. The metabolome of liver was detected by ultra-high performance liquid chromatography-mass spectrometry(UPLC-MS) after extraction by 80% methanol. Principal component analysis (PCA), differential metabolite analysis and KEGG pathway enrichment analysis were performed to find the metabolic changes in the liver of obese mice. Results After 24 weeks of high fat diet, the body weight and liver weight of HFD group mice were much higher than that of CD group mice. Besides, HFD group mice liver showed severe steatosis and slight fibrosis. There were also significant differences in liver metabolites between HFD and CD groups, and the metabolic changes were mainly enriched in pathways of phenylalanine metabolism, citric acid cycle (TCA cycle), sphingolipid metabolism, arginine biosynthesis and primary bile acid biosynthesis. Conclusions The obese mouse model was successfully constructed, and the pathological characteristics of obese mice liver were elucidated. At the same time,the main metabolic pathway changes of obese mice liver were further revealed by metabonomics analysis.

Key words: obesity, liver, metabolome, diet induction

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