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糖肾方通过AMPK/SIRT1通路诱导自噬减轻肝脂肪变性。

Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway.

作者信息

Wang Yan, Zhao Hailing, Li Xin, Li Nan, Wang Qian, Liu Yanzhen, Liang Qionglin, Shao Zixing, Zhang Nannan, Zhao Tingting, Peng Liang, Li Ping

机构信息

Beijing Key Laboratory for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing, China.

Graduate School of Peking Union Medical College, Chinese Academy of Medical Science & Peking Union Medical College, Beijing, China.

出版信息

Front Physiol. 2019 Apr 26;10:494. doi: 10.3389/fphys.2019.00494. eCollection 2019.

Abstract

Tangshen formula (TSF), a formula of Chinese herbal medicine, improves lipid metabolism in humans and animals with diabetic kidney disease. However, the effect and mechanism of TSF on nonalcoholic fatty liver disease (NAFLD) remain unclear. The activation of autophagy appears to be a potential mechanism for improving NAFLD. In the present study, we examined the therapeutic effect of TSF on hepatic steatosis and sought to explore whether its effect is related to activating autophagy. Here, we showed that TSF treatment significantly attenuated hepatic steatosis in both high-fat diet (HFD) and methionine choline-deficient diet (MCDD)-fed mice. Meanwhile, TSF reduced lipid accumulation in palmitate (PA)-stimulated HepG2 cells and primary mouse hepatocytes. Furthermore, TSF increased Sirtuin 1 (SIRT1) expression and promoted autophagy activation . TSF also improved PA-induced suppression of both SIRT1 expression and SIRT1-dependent autophagy, thereby alleviating intracellular lipid accumulation . In addition, TSF increased SIRT1 expression and induced autophagy in an adenosine monophosphate-activated protein kinase (AMPK)-dependent manner. Moreover, SIRT1 knockdown abolished the autophagy-inducing and lipid-lowering effects of TSF. In conclusion, TSF improved lipid accumulation and hepatic steatosis by inducing the AMPK/SIRT1 pathway-mediated autophagy.

摘要

糖肾方(TSF)是一种中药配方,可改善糖尿病肾病患者和动物的脂质代谢。然而,TSF对非酒精性脂肪性肝病(NAFLD)的作用及机制尚不清楚。自噬的激活似乎是改善NAFLD的潜在机制。在本研究中,我们检测了TSF对肝脂肪变性的治疗效果,并试图探讨其作用是否与激活自噬有关。在此,我们发现TSF治疗显著减轻了高脂饮食(HFD)和蛋氨酸胆碱缺乏饮食(MCDD)喂养小鼠的肝脂肪变性。同时,TSF减少了棕榈酸(PA)刺激的HepG2细胞和原代小鼠肝细胞中的脂质积累。此外,TSF增加了沉默调节蛋白1(SIRT1)的表达并促进了自噬激活。TSF还改善了PA诱导的SIRT1表达抑制和SIRT1依赖性自噬,从而减轻细胞内脂质积累。此外,TSF以腺苷单磷酸激活蛋白激酶(AMPK)依赖性方式增加SIRT1表达并诱导自噬。此外,SIRT1基因敲低消除了TSF的自噬诱导和降脂作用。总之,TSF通过诱导AMPK/SIRT1途径介导的自噬改善脂质积累和肝脂肪变性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e07/6498888/fe77d1b32380/fphys-10-00494-g001.jpg

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