钟丽萍, 李瑾, 王凤忠, 朱海波, 侯旭杰. 虫草素对ob/ob小鼠非酒精性脂肪肝的改善作用及机制研究J. 药学学报, 2017,52(1): 106-112. doi: 10.16438/j.0513-4870.2016-0886
引用本文: 钟丽萍, 李瑾, 王凤忠, 朱海波, 侯旭杰. 虫草素对ob/ob小鼠非酒精性脂肪肝的改善作用及机制研究J. 药学学报, 2017,52(1): 106-112. doi: 10.16438/j.0513-4870.2016-0886
ZHONG Li-ping, LI Jin, WANG Feng-zhong, ZHU Hai-bo, HOU Xu-jie. Protective effect and underlying mechanism of cordycepin on non-alcoholic fatty liver in ob/ob miceJ. Acta Pharmaceutica Sinica, 2017,52(1): 106-112. doi: 10.16438/j.0513-4870.2016-0886
Citation: ZHONG Li-ping, LI Jin, WANG Feng-zhong, ZHU Hai-bo, HOU Xu-jie. Protective effect and underlying mechanism of cordycepin on non-alcoholic fatty liver in ob/ob miceJ. Acta Pharmaceutica Sinica, 2017,52(1): 106-112. doi: 10.16438/j.0513-4870.2016-0886

虫草素对ob/ob小鼠非酒精性脂肪肝的改善作用及机制研究

Protective effect and underlying mechanism of cordycepin on non-alcoholic fatty liver in ob/ob mice

  • 摘要: 探讨虫草素对ob/ob小鼠非酒精性脂肪肝的改善作用及保护机制。将12周龄的雄性B6.V-Lepob/Lepob小鼠,按照血糖和体重分层后随机分为5组,并以C57BL/6J小鼠为对照组。每周监测一次体重和摄食,在给药2周和4周时,眼眶静脉取血测定血清中的各项生化指标,在给药5周时,进行胰岛素耐量实验,在给药7周后取肝脏组织对甘油三酯、胆固醇及炎症因子含量进行检测,并进行苏木精-伊红染色和油红O染色;提取肝组织的总RNA,采用实时定量PCR技术分析与脂质合成和炎症相关基因的表达。结果显示,虫草素可以有效降低ob/ob小鼠血脂水平,改善肝功能,明显降低肝脏组织脂质含量和炎症因子水平,而对胰岛素抵抗未见改善作用。实时定量PCR结果表明,虫草素可显著降低ob/ob小鼠肝脏组织中与脂质合成及炎症相关mRNA的表达。结果提示,虫草素对ob/ob小鼠非酒精性脂肪肝具有改善作用,其作用机制可能与下调脂质合成和炎症相关基因表达有关。

     

    Abstract: This study is designed to investigate the protective effect and mechanism of cordycepin on nonalcoholic fatty liver in ob/ob mice. Twelve-week-old male ob/ob mice were divided into 5 groups according to their body weight and blood glucose, and C57BL/6J mice were used in the control group. The animals were orally administered with cordycepin for 7 weeks. Body weight and food intake were measured once a week. Blood were collected from ophthalmic venous and biochemical indexes were determined at the 2nd and 4th week. Insulin tolerance test was performed at the 5th week. After 7 weeks of administration, liver tissues were collected to determine the contents of triglycerides and total cholesterol, and pro-inflammatory cytokines. Liver histology was performed by hematoxylin-eosin and oil-red O staining. Total RNA were extracted from liver tissues and the levels of lipid metabolism-related and inflammation-related genes were detected by real time PCR. Cordycepin effectively reduced the blood lipids level and improved liver function. Nevertheless, it did not improve insulin resistance in ob/ob mice. Cordycepin significantly reduced the contents of triglycerides and cholesterol, and the levels of pro-inflammatory cytokines in liver tissues. Moreover, cordycepin remarkably suppressed the expression of genes related to lipids synthesis and inflammation. These results indicate that cordycepin may improve non-alcoholic fatty liver in ob/ob mice, and the underlying mechanism may be associated with decreased expression of genes related to lipids synthesis and inflammation.

     

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