Cytotoxicity of Oleandrin Is Mediated by Calcium Influx and by Increased Manganese Uptake in Saccharomyces cerevisiae Cells

Molecules. 2020 Sep 17;25(18):4259. doi: 10.3390/molecules25184259.

Abstract

Oleandrin, the main component of Nerium oleander L. extracts, is a cardiotoxic glycoside with multiple pharmacological implications, having potential anti-tumoral and antiviral characteristics. Although it is accepted that the main mechanism of oleandrin action is the inhibition of Na+/K+-ATPases and subsequent increase in cell calcium, many aspects which determine oleandrin cytotoxicity remain elusive. In this study, we used the model Saccharomyces cerevisiae to unravel new elements accounting for oleandrin toxicity. Using cells expressing the Ca2+-sensitive photoprotein aequorin, we found that oleandrin exposure resulted in Ca2+ influx into the cytosol and that failing to pump Ca2+ from the cytosol to the vacuole increased oleandrin toxicity. We also found that oleandrin exposure induced Mn2+ accumulation by yeast cells via the plasma membrane Smf1 and that mutants with defects in Mn2+ homeostasis are oleandrin-hypersensitive. Our data suggest that combining oleandrin with agents which alter Ca2+ or Mn2+ uptake may be a way of controlling oleandrin toxicity.

Keywords: Saccharomyces cerevisiae; calcium; manganese; oleandrin.

MeSH terms

  • Calcium / metabolism*
  • Cardenolides / chemistry*
  • Cardenolides / pharmacology
  • Cardiac Glycosides / chemistry*
  • Cardiac Glycosides / metabolism*
  • Cardiac Glycosides / pharmacology
  • Cell Membrane Permeability
  • Cell Survival / drug effects
  • Cytosol / metabolism
  • Cytosol / ultrastructure
  • Enzyme Inhibitors / metabolism
  • Humans
  • Manganese / metabolism*
  • Saccharomyces cerevisiae / drug effects*
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Spectrometry, Fluorescence

Substances

  • Cardenolides
  • Cardiac Glycosides
  • Enzyme Inhibitors
  • Manganese
  • Sodium-Potassium-Exchanging ATPase
  • oleandrin
  • Calcium