Persistent overexpression of phosphoglycerate mutase, a glycolytic enzyme, modifies energy metabolism and reduces stress resistance of heart in mice

PLoS One. 2013 Aug 12;8(8):e72173. doi: 10.1371/journal.pone.0072173. eCollection 2013.

Abstract

Background: Heart failure is associated with changes in cardiac energy metabolism. Glucose metabolism in particular is thought to be important in the pathogenesis of heart failure. We examined the effects of persistent overexpression of phosphoglycerate mutase 2 (Pgam2), a glycolytic enzyme, on cardiac energy metabolism and function.

Methods and results: Transgenic mice constitutively overexpressing Pgam2 in a heart-specific manner were generated, and cardiac energy metabolism and function were analyzed. Cardiac function at rest was normal. The uptake of analogs of glucose or fatty acids and the phosphocreatine/βATP ratio at rest were normal. A comprehensive metabolomic analysis revealed an increase in the levels of a few metabolites immediately upstream and downstream of Pgam2 in the glycolytic pathway, whereas the levels of metabolites in the initial few steps of glycolysis and lactate remained unchanged. The levels of metabolites in the tricarboxylic acid (TCA) cycle were altered. The capacity for respiration by isolated mitochondria in vitro was decreased, and that for the generation of reactive oxygen species (ROS) in vitro was increased. Impaired cardiac function was observed in response to dobutamine. Mice developed systolic dysfunction upon pressure overload.

Conclusions: Constitutive overexpression of Pgam2 modified energy metabolism and reduced stress resistance of heart in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiotonic Agents / pharmacology
  • Dobutamine / pharmacology
  • Echocardiography
  • Energy Metabolism / genetics*
  • Enzyme Activation
  • Fibrosis
  • Gene Expression*
  • Glucose / metabolism
  • Glycolysis / genetics
  • Heart / diagnostic imaging
  • Heart / drug effects
  • Heart / physiopathology
  • Magnetic Resonance Spectroscopy
  • Male
  • Metabolome
  • Metabolomics / methods
  • Mice
  • Mice, Transgenic
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Organ Specificity / genetics
  • Phosphoglycerate Mutase / genetics*
  • Phosphoglycerate Mutase / metabolism
  • Radionuclide Imaging
  • Reactive Oxygen Species / metabolism
  • Stress, Physiological / genetics*

Substances

  • Cardiotonic Agents
  • Reactive Oxygen Species
  • Dobutamine
  • Phosphoglycerate Mutase
  • Glucose

Grants and funding

This work was supported by the Japan Society for the Promotion of Science, the Vehicle Racing Commemorative Foundation, and the Innovative Techno-Hub for Integrated Medical Bio-imaging Project of the Special Coordination Funds for Promoting Science and Technology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.