Wiegand V, Stroh E, Henniges A, Lossnitzer K, Kreuzer H
Basic Res Cardiol. 1983 Nov-Dec;78(6):665-70. doi: 10.1007/BF01907213.
Myosin of the ventricular myocardium of the cardiomyopathic Syrian hamster and of control animals was analysed using non-dissociating pyrophosphate electrophoresis. Three different myosin isoenzymes exhibiting different Ca2+ activated ATPase activities were demonstrated in the ventricular myocardium of the Syrian hamster. As shown by peptide mapping, ventricular myosin isoenzymes differ in their heavy chain composition. In the cardiomyopathic hamster a shift to myosins of lower Ca2+-activated ATPase activities occurs in the stage of insufficiency (age 220 days), whereas no different isoenzyme pattern could be found at the age of 65 days compared to control animals. We conclude that this redistribution of myosin isoenzymes is the basis of reduced myosin ATPase activity in the ventricular myocardium of the cardiomyopathic Syrian hamster during the development of myocardial insufficiency.
采用非解离性焦磷酸电泳法分析了患心肌病的叙利亚仓鼠及对照动物心室肌的肌球蛋白。在叙利亚仓鼠的心室肌中证实存在三种不同的肌球蛋白同工酶,它们表现出不同的Ca2+激活的ATP酶活性。肽图分析表明,心室肌球蛋白同工酶的重链组成不同。在患心肌病的仓鼠中,在功能不全阶段(220日龄)出现了向较低Ca2+激活的ATP酶活性的肌球蛋白的转变,而在65日龄时,与对照动物相比未发现不同的同工酶模式。我们得出结论,这种肌球蛋白同工酶的重新分布是患心肌病的叙利亚仓鼠在心肌功能不全发展过程中心室肌肌球蛋白ATP酶活性降低的基础。