A transient increase in lipid peroxidation primes preadipocytes for delayed mitochondrial inner membrane permeabilization and ATP depletion during prolonged exposure to fatty acids

Free Radic Biol Med. 2014 Feb:67:330-41. doi: 10.1016/j.freeradbiomed.2013.11.012. Epub 2013 Nov 22.

Abstract

Preadipocytes are periodically subjected to fatty acid (FA) concentrations that are potentially cytotoxic. We tested the hypothesis that prolonged exposure of preadipocytes of human origin to a physiologically relevant mix of FAs leads to mitochondrial inner membrane (MIM) permeabilization and ultimately to mitochondrial crisis. We found that exposure of preadipocytes to FAs led to progressive cyclosporin A-sensitive MIM permeabilization, which in turn caused a reduction in MIM potential, oxygen consumption, and ATP synthetic capacity and, ultimately, death. Additionally, we showed that FAs induce a transient increase in intramitochondrial reactive oxygen species (ROS) and lipid peroxide production, lasting roughly 30 and 120min for the ROS and lipid peroxides, respectively. MIM permeabilization and its deleterious consequences including mitochondrial crisis and cell death were prevented by treating the cells with the mitochondrial FA uptake inhibitor etomoxir, the mitochondrion-selective superoxide and lipid peroxide antioxidants MitoTempo and MitoQ, or the lipid peroxide and reactive carbonyl scavenger l-carnosine. FAs also promoted a delayed oxidative stress phase. However, the beneficial effects of etomoxir, MitoTempo, and l-carnosine were lost by delaying the treatment by 2h, suggesting that the initial phase was sufficient to prime the cells for the delayed MIM permeabilization and mitochondrial crisis. It also suggested that the second ROS production phase is a consequence of this loss in mitochondrial health. Altogether, our data suggest that approaches designed to diminish intramitochondrial ROS or lipid peroxide accumulation, as well as MIM permeabilization, are valid mechanism-based therapeutic avenues to prevent the loss in preadipocyte metabolic fitness associated with prolonged exposure to elevated FA levels.

Keywords: ATP; Bioenergetic; Fatty acids; Free radicals; H(2)O(2); Lipid peroxidation; Mitochondria; Mitochondrial inner membrane permeability; Mitochondrial inner membrane potential; Preadipocytes; Respiration; Superoxide.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / antagonists & inhibitors
  • Adenosine Triphosphate / metabolism*
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Carnosine / pharmacology
  • Cell Death / drug effects
  • Cell Differentiation
  • Cell Line, Transformed
  • Cyclosporine / pharmacology
  • Epoxy Compounds / pharmacology
  • Fatty Acids / pharmacology*
  • Gene Expression
  • Humans
  • Lipid Peroxidation / drug effects
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitochondrial Membranes / drug effects*
  • Mitochondrial Membranes / metabolism
  • Organophosphorus Compounds / pharmacology
  • Oxidative Stress
  • Permeability
  • Piperidines / pharmacology
  • Reactive Oxygen Species / metabolism
  • Superoxides / pharmacology
  • Ubiquinone / analogs & derivatives
  • Ubiquinone / pharmacology

Substances

  • Epoxy Compounds
  • Fatty Acids
  • MitoTEMPO
  • Organophosphorus Compounds
  • Piperidines
  • Reactive Oxygen Species
  • Superoxides
  • Ubiquinone
  • mitoquinone
  • Cyclosporine
  • Carnosine
  • Adenosine Triphosphate
  • etomoxir