[Zexie Decoction regulates Akt/TFEB signaling pathway to promote lipophagy in hepatocytes]

Zhongguo Zhong Yao Za Zhi. 2022 Nov;47(22):6183-6190. doi: 10.19540/j.cnki.cjcmm.20220706.702.
[Article in Chinese]

Abstract

Taking lipophagy as the breakthrough point, we explored the mechanism of Zexie Decoction(ZXD) in improving lipid metabolism in the hepatocyte model induced by palmitic acid(PA) and in the animal model induced by high-fat diet(HFD) on the basis of protein kinase B(Akt)/transcription factor EB(TFEB) signaling pathway. Co-localization was carried out for the microtubule-associated protein light chain 3(LC3) plasmid labeled with green fluorescent protein(GFP) and lipid droplets(LDs), and immunofluorescence co-localization for liver LC3 of HFD mice and perilipin 2(PLIN2). The results showed that ZXD up-regulated the expression of LC3, reduced lipid accumulation in hepatocytes, and increased the co-localization of LC3 and LDs, thereby activating lipo-phagy. Western blot results confirmed that ZXD increased autophagy-related protein LC3Ⅱ/LC3Ⅰ transformation ratio and lysosome-associated membrane protein 2(LAMP2) in vivo and in vitro and promoted the degradation of sequestosome-1(SQSTM1/p62)(P<0.05). The results above jointly explained that ZXD regulated lipophagy. Furthermore, ZXD activated TFEB expression(P<0.05) and reversed the PA-and HFD-induced decrease of TFEB nuclear localization in hepatocytes(P<0.05). Meanwhile, ZXD activated liver TFEB to up-regulate the expression of the targets Lamp2, Lc3 B, Bcl2, and Atg5(P<0.05). Additionally, ZXD down-regulated the protein level of p-Akt upstream of TFEB in vivo and in vitro. In conclusion, ZXD may promote lipophagy by regulating the Akt/TFEB pathway.

Keywords: Akt/TFEB pathway; Zexie Decoction; lipophagy.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Autophagy* / drug effects
  • Drugs, Chinese Herbal* / pharmacology
  • Hepatocytes* / drug effects
  • Hepatocytes* / metabolism
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Proto-Oncogene Proteins c-akt* / genetics
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Signal Transduction

Substances

  • Microtubule-Associated Proteins
  • Proto-Oncogene Proteins c-akt
  • Drugs, Chinese Herbal