王凯, 柳星峰, 李平平. 胰岛素抵抗状态下肝脏脂质合成增加的研究进展J. 药学学报, 2020,55(2): 189-194. doi: 10.16438/j.0513-4870.2019-0718
引用本文: 王凯, 柳星峰, 李平平. 胰岛素抵抗状态下肝脏脂质合成增加的研究进展J. 药学学报, 2020,55(2): 189-194. doi: 10.16438/j.0513-4870.2019-0718
WANG Kai, LIU Xing-feng, LI Ping-ping. Advances in molecular mechanisms for enhanced hepatic lipogenesis in insulin resistanceJ. Acta Pharmaceutica Sinica, 2020,55(2): 189-194. doi: 10.16438/j.0513-4870.2019-0718
Citation: WANG Kai, LIU Xing-feng, LI Ping-ping. Advances in molecular mechanisms for enhanced hepatic lipogenesis in insulin resistanceJ. Acta Pharmaceutica Sinica, 2020,55(2): 189-194. doi: 10.16438/j.0513-4870.2019-0718

胰岛素抵抗状态下肝脏脂质合成增加的研究进展

Advances in molecular mechanisms for enhanced hepatic lipogenesis in insulin resistance

  • 摘要: 肝脏选择性胰岛素抵抗是胰岛素抵抗状态下,胰岛素在肝脏不能抑制糖异生进而导致葡萄糖产生增加,但同时脂质合成过程保持亢进的状态。正是这种亢进状态导致2型糖尿病患者除高血糖外还伴随高血脂。本文通过固醇调节因子结合蛋白1c(SREBP1c)、哺乳动物雷帕霉素靶复合体1(mTORC1)、内质网应激、FOXO1、脂质合成底物等促进肝脏脂质合成的相关研究,综述胰岛素抵抗状态下肝脏脂质合成增加的分子机制研究进展。

     

    Abstract: Hepatic selective insulin resistance refers to that insulin fails to suppress hepatic glucose production but continues to promote hepatic lipogenesis in insulin resistance. Therefore, type 2 diabetes mellitus is characterized with dyslipidemia apart from hyperglycemia. This review highlights the roles and molecular mechanisms of the key hepatic lipogenesis factors such as sterol regulatory factor binding protein 1c (SREBP1c), mammalian rapamycin target complex 1 (mTORC1), endoplasmic reticulum stress (ER stress), FoxO1, lipid synthesis substrate, etc.

     

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