Myocardial expression of the arginine:glycine amidinotransferase gene is elevated in heart failure and normalized after recovery: Potential implications for local creatine synthesis

Martin E. Cullen, Ada H.Y. Yuen, Leanne E. Felkin, Ryszard T. Smolenski, Jennifer L Hall, Suzanne Grindle, Leslie W. Miller, Emma J. Birks, Magdi H. Yacoub, Paul J.R. Barton

Research output: Contribution to journalArticlepeer-review

80 Scopus citations

Abstract

BACKGROUND - Combination therapy consisting of mechanical unloading using a left ventricular assist device (LVAD) and pharmacological intervention can promote recovery from end-stage heart failure, but the mechanism is unknown. Preliminary microarray analysis revealed a significant and unexpected decrease in myocardial arginine:glycine amidinotransferase (AGAT) gene expression during recovery in these patients. The aim of this study was to evaluate the expression and role of AGAT expression in heart failure and recovery. METHODS AND RESULTS - We used quantitative real time (TaqMan) polymerase chain reaction to examine myocardial AGAT mRNA expression in implant and explant samples from recovering patients after combination therapy (n=12), end-stage heart failure (ESHF) samples from stable patients undergoing transplantation without LVAD support (n=10), and donor hearts with normal hemodynamic function (n=8). AGAT mRNA expression was significantly elevated in all heart failure patients relative to donors (4.3-fold [P<0.001] and 2.7-fold [P<0.005] in LVAD and ESHF relative to donors, respectively) and returned to normal levels after recovery. AGAT enzyme activity was detectable in both human and rat myocardia and was elevated in heart failure. CONCLUSIONS - Our data highlight local and potentially regulated expression of AGAT activity in the myocardium and suggest a specific response to heart failure involving elevated local creatine synthesis. These findings have implications both for the management of recovery patients undergoing combination therapy and for heart failure in general.

Original languageEnglish (US)
Pages (from-to)I16-I20
JournalCirculation
Volume114
Issue numberSUPPL. 1
DOIs
StatePublished - Jul 2006

Keywords

  • Genes
  • Heart-assist device
  • Metabolism
  • Myocardium
  • Remodeling

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