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  2. Scutellarin ameliorates hepatic lipid accumulation by enhancing autophagy and suppressing IRE1α/XBP1 pathway

Scutellarin ameliorates hepatic lipid accumulation by enhancing autophagy and suppressing IRE1α/XBP1 pathway

  • Phytother Res. 2022 Jan;36(1):433-447. doi: 10.1002/ptr.7344.
Xueying Zhang 1 Zhaojiong Huo 1 Huiling Luan 1 Yihai Huang 1 Yanhui Shen 1 Liang Sheng 2 Jiangyu Liang 1 Feihua Wu 1
Affiliations

Affiliations

  • 1 School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.
  • 2 School of Basic Medical Science, Nanjing Medical University, Nanjing, China.
Abstract

Nonalcoholic fatty liver disease is the most prevalent liver disease characterized by excessive lipid accumulation in hepatocytes. Endoplasmic reticulum (ER) stress and Autophagy play an important role in lipid accumulation. In this study, scutellarin (Scu) was examined in palmitic acid-treated HepG2 cells and C57/BL6 mice fed a high-fat diet (HFD). Scu reduced intracellular lipid content and inhibited sterol regulatory element binding protein-1c (SREBP-1c)-mediated lipid synthesis and fatty acid translocase-mediated lipid uptake in HepG2 cells. Additionally, Scu restored impaired Autophagy and inhibited excessive activation of ER stress in vivo and in vitro. Moreover, Scu upregulated forkhead box O transcription factor 1-mediated Autophagy by inhibiting inositol-requiring Enzyme 1α (IRE1α)/X-box-binding protein 1 (XBP1) branch activation, while XBP1s overexpression exacerbated the lipid accumulation and impaired Autophagy in HepG2 cells and also weakened the positive effects of Scu. Furthermore, Scu attenuated ER stress by activating Autophagy, ultimately downregulating SREBP-1c-mediated lipid synthesis, and Autophagy inhibitors offset these beneficial effects. Scu inhibited the crosstalk between Autophagy and ER stress and downregulated saturated fatty acid-induced lipid accumulation in hepatocytes. These findings demonstrate that Scu ameliorates hepatic lipid accumulation by enhancing Autophagy and suppressing ER stress via the IRE1α/XBP1 pathway.

Keywords

XBP1s; autophagy; endoplasmic reticulum stress; nonalcoholic fatty liver disease; scutellarin.

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