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Accueil > Publications > Recherche par années > Années 1990 > 1997

Stepanov, V ; Mateo, P ; Gillet, B ; Beloeil, JC ; Lechene, P ; Hoerter, JA

Kinetics of creatine kinase in an experimental model of low phosphocreatine and ATP in the normoxic heart

American Journal of Physiology-Cell Physiology 273 (4) C1397-C1408

par Administrateur - publié le

Abstract :

To study the dependence of the forward flux of creatine kinase (CK) on its substrates and products we designed an acute normoxic model of steady-state depletion of phosphocreatine (PCr) and adenylate in the isovolumic acetate-perfused rat heart. Various concentrations of PCr and ATP were induced by prior perfusion with 2 deoxy-D-glucose in the presence of insulin. The apparent rate constant (K-f) and the forward CK flux were measured under metabolic and contractile steady state by progressive saturation-transfer P-31 nuclear magnetic resonance (NMR). At high adenylate content CK flux was constant for a twofold reduction in PCr concentration ([PCr]) ; CK flux was 6.3 +/- 0.6 mM/s (vs. 6.5 +/- 0.2 mM/s in control) because of a doubling of k(f). Although, at the lowest ATP concentration and [PCr], CK flux was reduced by 50%, it nevertheless always remained higher than ATP synthesis estimated by parallel oxygen consumption measurement. NMR-measured flux was compared with the flux computed under the hypothesis of CK equilibrium. CK flux could not be fully predicted by the concentrations of CK metabolites. This is discussed in terms of metabolite and CK isozyme compartmentation.