Schisandrin B mitigates hepatic steatosis and promotes fatty acid oxidation by inducing autophagy through AMPK/mTOR signaling pathway

Metabolism. 2022 Jun:131:155200. doi: 10.1016/j.metabol.2022.155200. Epub 2022 Apr 8.

Abstract

Background: Schisandrin B (Sch B), which inhibits hepatic steatosis caused by non-alcoholic fatty liver disease (NAFLD), is one of the most active dibenzocyclooctadienes isolated from Schisandra chinensis (Turcz.) Baill with various pharmacological activities. In this study, the role of Sch B-induced autophagy in lipid-lowering activities of Sch B was examined and the underlying mechanisms were elucidated.

Methods: Free fatty acid (FFA)-stimulated HepG2 cells and mouse primary hepatocytes (MPHs) and high-fat diet (HFD)-fed mice were used as NAFLD models. The role of Sch B-induced autophagy in lipid-lowering effects of Sch B was assessed using ATG5/TFEB-deficient cells and 3-methyladenine (3-MA)-treated hepatocytes and mice.

Results: Sch B simultaneously active autophagy through AMPK/mTOR pathway and decreased the number of lipid droplets in FFA-treated HepG2 cells and MPHs. Additionally, siATG5/siTFEB transfection or 3-MA treatment mitigated Sch B-induced autophagy and activation of fatty acid oxidation (FAO) and ketogenesis in FFA-treated HepG2 cells and MPHs. Sch B markedly decreased hepatic lipid content and activated the autophagy through AMPK/mTOR pathway in HFD-fed mice. However, the activities of Sch B were suppressed upon 3-MA treatment. Sch B upregulated the expression of key enzymes involved in FAO and ketogenesis, which was mitigated upon 3-MA treatment. Moreover, changes in hepatic lipid components and amino acids may be related to the Sch B-induced autophagy pathway.

Conclusion: These results suggested that Sch B inhibited hepatic steatosis and promoted FAO by activation of autophagy through AMPK/mTOR pathway. Our study provides novel insights into the hepatic lipophagic activity of Sch B and its potential application in the management of NAFLD.

Keywords: Autophagy; Lipid metabolism; Non-alcoholic fatty liver disease; Schisandrin B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Animals
  • Autophagy
  • Cyclooctanes
  • Diet, High-Fat
  • Fatty Acids, Nonesterified / metabolism
  • Hepatocytes / metabolism
  • Ketone Bodies / metabolism
  • Lignans
  • Lipid Metabolism
  • Liver / metabolism
  • Mice
  • Non-alcoholic Fatty Liver Disease* / metabolism
  • Polycyclic Compounds
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Cyclooctanes
  • Fatty Acids, Nonesterified
  • Ketone Bodies
  • Lignans
  • Polycyclic Compounds
  • schizandrin B
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases