Increasing fatty acid oxidation elicits a sex-dependent response in failing mouse hearts

J Mol Cell Cardiol. 2021 Sep:158:1-10. doi: 10.1016/j.yjmcc.2021.05.004. Epub 2021 May 12.

Abstract

Background: Reduced fatty acid oxidation (FAO) is a hallmark of metabolic remodeling in heart failure. Enhancing mitochondrial long-chain fatty acid uptake by Acetyl-CoA carboxylase 2 (ACC2) deletion increases FAO and prevents cardiac dysfunction during chronic stresses, but therapeutic efficacy of this approach has not been determined.

Methods: Male and female ACC2 f/f-MCM (ACC2KO) and their respective littermate controls were subjected to chronic pressure overload by TAC surgery. Tamoxifen injection 3 weeks after TAC induced ACC2 deletion and increased FAO in ACC2KO mice with pathological hypertrophy.

Results: ACC2 deletion in mice with pre-existing cardiac pathology promoted FAO in female and male hearts, but improved cardiac function only in female mice. In males, pressure overload caused a downregulation in the mitochondrial oxidative function. Stimulating FAO by ACC2 deletion caused unproductive acyl-carnitine accumulation, which failed to improve cardiac energetics. In contrast, mitochondrial oxidative capacity was sustained in female pressure overloaded hearts and ACC2 deletion improved myocardial energetics. Mechanistically, we revealed a sex-dependent regulation of PPARα signaling pathway in heart failure, which accounted for the differential response to ACC2 deletion.

Conclusion: Metabolic remodeling in the failing heart is sex-dependent which could determine the response to metabolic intervention. The findings suggest that both mitochondrial oxidative capacity and substrate preference should be considered for metabolic therapy of heart failure.

Keywords: Energy metabolism; Fatty acid oxidation; Heart failure.

Publication types

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

MeSH terms

  • Acetyl-CoA Carboxylase / genetics
  • Acetyl-CoA Carboxylase / metabolism*
  • Animals
  • Carnitine / analogs & derivatives
  • Carnitine / metabolism
  • Disease Models, Animal
  • Energy Metabolism / drug effects
  • Energy Metabolism / genetics
  • Fatty Acids / metabolism*
  • Female
  • Gene Deletion
  • Heart Failure / genetics
  • Heart Failure / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Myocardium / metabolism
  • Oxidation-Reduction
  • PPAR alpha / metabolism*
  • Sex Factors
  • Signal Transduction / drug effects
  • Signal Transduction / genetics*
  • Tamoxifen / administration & dosage

Substances

  • Fatty Acids
  • PPAR alpha
  • Ppara protein, mouse
  • acylcarnitine
  • Tamoxifen
  • Acacb protein, mouse
  • Acetyl-CoA Carboxylase
  • Carnitine