Omentin-1 mitigates non-alcoholic fatty liver disease by preserving autophagy through AMPKα/mTOR signaling pathway

Sci Rep. 2024 Dec 28;14(1):31464. doi: 10.1038/s41598-024-83112-0.

Abstract

Adipose tissue-derived adipokines facilitate inter-organ communication between adipose tissue and other organs. Omentin-1, an adipokine, has been implicated in the regulation of glucose and insulin metabolism. However, limited knowledge exists regarding the regulatory impact of endogenous omentin-1 on hepatic steatosis. C57BL/6J mice were fed with high-fat diet (HFD) for 8 weeks to induce nonalcoholic fatty liver disease (NAFLD), while HepG2 cells were exposed to a 0.1 mM free fatty acid (FFA) mixture for 24 h to induce hepatic steatosis. Both the mice and cells were treated with omentin-1, and the therapeutic effects as well as the underlying molecular mechanisms were investigated. Our data demonstrate that omentin-1 attenuates weight and fat mass gain, preserves glucose homeostasis, normalizes the expression of lipogenesis-related proteins, and alleviates hepatic lipid accumulation in HFD fed mice. Furthermore, omentin-1 normalized AMPKα/mTOR signaling and preserves autophagy in these mice. In vitro, omentin-1 also preserves autophagy and attenuates lipid accumulation by normalizing AMPKα/mTOR signaling in a cell model of FFA treated HepG2 cells. However, inhibition of AMPK with Compound C or AMPKα whole-body knockout reverses the above beneficial effects of omentin-1. The present study demonstrates that omentin-1 exerts a preventive effect on non-alcoholic fatty liver disease (NAFLD) by preserving autophagy through normalizing the AMPKα/mTOR pathway, thereby suggesting its potential as a promising therapeutic agent against NAFLD.

Keywords: AMPK; Autophagy; Nonalcoholic fatty liver disease; Omentin-1; mTOR.

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Animals
  • Autophagy*
  • Cytokines* / metabolism
  • Diet, High-Fat / adverse effects
  • Disease Models, Animal
  • GPI-Linked Proteins* / metabolism
  • Hep G2 Cells
  • Humans
  • Lectins* / metabolism
  • Lectins* / pharmacology
  • Lipid Metabolism
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Non-alcoholic Fatty Liver Disease* / metabolism
  • Non-alcoholic Fatty Liver Disease* / pathology
  • Signal Transduction*
  • TOR Serine-Threonine Kinases* / metabolism

Substances

  • Cytokines
  • AMP-Activated Protein Kinases
  • TOR Serine-Threonine Kinases
  • Lectins
  • GPI-Linked Proteins
  • Itln1 protein, mouse