Effects of MCI-154, a calcium sensitizer, on left ventricular systolic and diastolic function in pacing-induced heart failure in the dog

被引:22
|
作者
Teramura, S [1 ]
Yamakado, T [1 ]
Maeda, M [1 ]
Nakano, T [1 ]
机构
[1] MIE UNIV, DEPT INTERNAL MED 1, TSU, MIE 514, JAPAN
关键词
calcium; heart failure; systole; diastole; inotropic agents;
D O I
10.1161/01.CIR.95.3.732
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background MCI-154 is a positive inotropic agent that increases the myofilament response to Ca2+. Whether MCI-154 has beneficial effects on left ventricular dysfunction in chronic heart failure is not known. We examined the effects of MCI-154 on left ventricular systolic and diastolic function in pacing-induced heart failure in dogs. Methods and Results We studied eight anesthetized dogs before and 2 to 4 weeks after rapid right ventricular pacing. Left cineventriculograms with simultaneous left ventricular pressures (tip manometer) were obtained before and during intravenous administration of MCI-154 (1.0 mu g . kg(-1). min(-1) for 15 minutes) in the control and heart-failure states. Left ventricular volume dynamics was derived from frame-by-frame (20-ms) analyses of left ventricular angiograms. In heart failure, left ventricular contractility as assessed by shifts of the end-systolic pressure-volume ratio, evaluated by inferior vena cava occlusion, was improved by MCI-154 (+1.94 mm Hg/mL, P<.05) to an extent similar to that in the control state (+2.47 mm Hg/mL, P<.05). MCI-154 also accelerated left ventricular relaxation, assessed by the time constant of isovolumic pressure decay (T-1/2), in both states. The absolute decrease in T-1/2 With MCI-154 in heart failure was significantly greater than in the control state (-8.2 versus -3.1 ms, P<.05). In heart failure, MCI-154 shifted the left ventricular diastolic pressure-volume relation clearly downward, suggesting increased diastolic distensibility. Conclusions MCI-154 improved not only left ventricular systolic function but also diastolic relaxation and distensibility in a chronic heart failure model.
引用
收藏
页码:732 / 739
页数:8
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