Reduced Inotropic Reserve and Increased Susceptibility to Cardiac Ischemia/Reperfusion Injury in Phosphocreatine-Deficient Guanidinoacetate- N -Methyltransferase–Knockout Mice
ten Hove M., Lygate CA., Fischer A., Schneider JE., Sang AE., Hulbert K., Sebag-Montefiore L., Watkins H., Clarke K., Isbrandt D., Wallis J., Neubauer S.
Background— The role of the creatine kinase (CK)/phosphocreatine (PCr) energy buffer and transport system in heart remains unclear. Guanidinoacetate- N -methyltransferase–knockout (GAMT −/− ) mice represent a new model of profoundly altered cardiac energetics, showing undetectable levels of PCr and creatine and accumulation of the precursor (phospho-)guanidinoacetate (P-GA). To characterize the role of a substantially impaired CK/PCr system in heart, we studied the cardiac phenotype of wild-type (WT) and GAMT −/− mice. Methods and Results— GAMT −/− mice did not show cardiac hypertrophy (myocyte cross-sectional areas, hypertrophy markers atrial natriuretic factor and β-myosin heavy chain). Systolic and diastolic function, measured invasively (left ventricular conductance catheter) and noninvasively (MRI), were similar for WT and GAMT −/− mice. However, during inotropic stimulation with dobutamine, preload-recruitable stroke work failed to reach maximal levels of performance in GAMT −/− hearts (101±8 mm Hg in WT versus 59±7 mm Hg in GAMT −/− ; P <0.05). 31 P-MR spectroscopy experiments showed that during inotropic stimulation, isolated WT hearts utilized PCr, whereas isolated GAMT −/− hearts utilized P-GA. During ischemia/reperfusion, GAMT −/− hearts showed markedly impaired recovery of systolic (24% versus 53% rate pressure product recovery; P <0.05) and diastolic function (eg, left ventricular end-diastolic pressure 23±9 in WT and 51±5 mm Hg in GAMT −/− during reperfusion; P <0.05) and incomplete resynthesis of P-GA. Conclusions— GAMT −/− mice do not develop hypertrophy and show normal cardiac function at low workload, suggesting that a fully functional CK/PCr system is not essential under resting conditions. However, when acutely stressed by inotropic stimulation or ischemia/reperfusion, GAMT −/− mice exhibit a markedly abnormal phenotype, demonstrating that an intact, high-capacity CK/PCr system is required for situations of increased cardiac work or acute stress.