Cardiospecific Overexpression of ATPGD1 (Carnosine Synthase) Increases Histidine Dipeptide Levels and Prevents Myocardial Ischemia Reperfusion Injury

J Am Heart Assoc. 2020 Jun 16;9(12):e015222. doi: 10.1161/JAHA.119.015222. Epub 2020 Jun 9.

Abstract

BACKGROUND Myocardial ischemia reperfusion (I/R) injury is associated with complex pathophysiological changes characterized by pH imbalance, the accumulation of lipid peroxidation products acrolein and 4-hydroxy trans-2-nonenal, and the depletion of ATP levels. Cardioprotective interventions, designed to address individual mediators of I/R injury, have shown limited efficacy. The recently identified enzyme ATPGD1 (Carnosine Synthase), which synthesizes histidyl dipeptides such as carnosine, has the potential to counteract multiple effectors of I/R injury by buffering intracellular pH and quenching lipid peroxidation products and may protect against I/R injury. METHODS AND RESULTS We report here that β-alanine and carnosine feeding enhanced myocardial carnosine levels and protected the heart against I/R injury. Cardiospecific overexpression of ATPGD1 increased myocardial histidyl dipeptides levels and protected the heart from I/R injury. Isolated cardiac myocytes from ATPGD1-transgenic hearts were protected against hypoxia reoxygenation injury. The overexpression of ATPGD1 prevented the accumulation of acrolein and 4-hydroxy trans-2-nonenal-protein adducts in ischemic hearts and delayed acrolein or 4-hydroxy trans-2-nonenal-induced hypercontracture in isolated cardiac myocytes. Changes in the levels of ATP, high-energy phosphates, intracellular pH, and glycolysis during low-flow ischemia in the wild-type mice hearts were attenuated in the ATPGD1-transgenic hearts. Two natural dipeptide analogs (anserine and balenine) that can either quench aldehydes or buffer intracellular pH, but not both, failed to protect against I/R injury. CONCLUSIONS Either exogenous administration or enhanced endogenous formation of histidyl dipeptides prevents I/R injury by attenuating changes in intracellular pH and preventing the accumulation of lipid peroxidation derived aldehydes.

Keywords: acrolein; anserine; balenine; carnosine; carnosine synthase; intracellular pH; ischemia reperfusion.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acrolein / metabolism
  • Adenosine Triphosphate / metabolism
  • Aldehydes / metabolism
  • Animals
  • Carnosine / metabolism*
  • Carnosine / pharmacology
  • Cell Hypoxia
  • Disease Models, Animal
  • Energy Metabolism
  • Hydrogen-Ion Concentration
  • Lipid Peroxidation / drug effects
  • Male
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Myocardial Infarction / enzymology
  • Myocardial Infarction / genetics
  • Myocardial Infarction / pathology
  • Myocardial Infarction / prevention & control*
  • Myocardial Reperfusion Injury / enzymology
  • Myocardial Reperfusion Injury / genetics
  • Myocardial Reperfusion Injury / pathology
  • Myocardial Reperfusion Injury / prevention & control*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / enzymology*
  • Myocytes, Cardiac / pathology
  • Peptide Synthases / genetics
  • Peptide Synthases / metabolism*
  • Up-Regulation
  • beta-Alanine / pharmacology

Substances

  • Aldehydes
  • beta-Alanine
  • Acrolein
  • Carnosine
  • Adenosine Triphosphate
  • Peptide Synthases
  • carnosine synthetase
  • 4-hydroxy-2-nonenal