Ginsenoside Re enhances the survival of H9c2 cardiac muscle cells through regulation of autophagy

J Asian Nat Prod Res. 2020 Aug;22(8):774-787. doi: 10.1080/10286020.2019.1632834. Epub 2019 Jun 22.

Abstract

We examined the effect of ginsenoside Re (G-Re) on autophagy in H9c2 cardiomyocytes cultured in glucose deprivation (GD). Levels of the membrane-bound autophagy-related microtubule-associated protein 1A/1B-light chain 3 (LC3) B-2 were measured via immunoblotting and immunofluorescence was conducted to assess autophagosome formation. GD H9c2 cells were treated with 100 μmol/l G-Re. Cell viability was determined in culture medium. Phosphorylated 5' AMP-activated protein kinase (AMPK)-α and mammalian target of rapamycin (mTOR) levels were measured to explore the mechanisms underlying the effects of G-Re on autophagy in GD cells. G-Re treatment inhibited autophagosome formation and may be beneficial to GD cardiomyocytes.

Keywords: AMPKα; Ginsenoside Re; H9c2 cells; autophagy; starvation.

MeSH terms

  • AMP-Activated Protein Kinases
  • Autophagy*
  • Cell Survival
  • Ginsenosides*
  • Molecular Structure
  • Myocytes, Cardiac

Substances

  • Ginsenosides
  • ginsenoside Re
  • AMP-Activated Protein Kinases