抄録
To understand the pathophysiology of hereditary cardiomyopathy, we measured the phosphorylation status of regulatory proteins, troponin I (TnI), troponin T (TnT), myosin light chain 2 (MLC2), and myosin-binding protein C (MyBP-C), and the Ca2+-dependence of tension development and ATPase activity in skinned right ventricular trabeculae obtained from cardiomyopathic (TO-2 strain, n = 8) and control (F1B strain, n = 8) hamsters. The Ca2+ sensitivities of tension development and ATPase activity (mean ± SD) were significantly (P < 0.0001) higher in the TO-2 strain (pCa50 5.64 ± 0.04 in tension and 5.65 ± 0.04 in ATPase activity) than in the F1B strain (pCa50 5.48 ± 0.03 in tension and 5.51 ± 0.03 in ATPase activity). No significant differences in their maximum values were observed between TO-2 (40.8 ± 7.4 mN/mm2 in tension and 0.52 ± 0.15 μmol/l/s in ATP consumption) and F1B (42.3 ± 8.5 mN/mm2 in tension and 0.58 ± 0.41 μmol/l/s in ATP consumption) preparations, indicating that the tension cost (ATPase activity/tension development) in TO-2 was quite similar to that in F1B. The phosphorylation levels of MLC2 and TnI were significantly (P < 0.01) lower in TO-2 than in F1B. These results suggest that the increase in the Ca2+ sensitivities of tension development and the ATPase activity in TO-2 hearts result from the decreased basal level of TnI phosphorylation, and these features can be considered to produce the incomplete diastolic relaxation and partly improve the systolic function in TO-2 hearts.
