Kitazawa T
J Biochem. 1976 Nov;80(5):1129-47. doi: 10.1093/oxfordjournals.jbchem.a131369.
It was investigated whether mitochondria play a significant role in the physiological regulation of the contractile process by Ca2+ in cardiac muscle in comparison with the sarcoplasmic reticulum (SR). Ca uptake activities of chicken cardiac SR and rabbit cardiac mitochondria were measured by means of centrifugation, dual-wave-length spectrophotometric and Millipore filtration methods. The maximum Ca uptake capacity of cardiac SR was usually 50-60 nmoles/mg protein and the apparent binding constant was 2.0 X 10(6) M-1. The apparent Ca-binding constant of cardiac mitochondria under limited loading conditions was 2.4 X 10(5) M-1 at pH 7.4 and 5.9 X 10(4) M-1 at pH 6.8. In the presence of 100 muM Ca2+ at 28-29 degrees, the estimated initial rate of Ca uptake of cardiac SR ranged from 20 to 30 nmoles Ca/mg-sec, while that of mitochondria was 4.6 nmoles Ca/mg-sec under limited loading conditions at pH 7.4 and 0.64 nmoles Ca/mg-sec under massive loading conditions at pH 6.8, which was much closer to physiological conditions. In the presence of low Ca2+ concentrations, the initial rate of Ca uptake of cardiac SR was 0.5 nmoles Ca/mg-sec at 3.5 X 10(-7) M Ca2+ and that of mitochondria under massive loading conditions at 1 X 10(-6) M Ca2+ was 0.02 nmoles Ca/mg-sec at pH 7.4 and 0.004 nmoles Ca/mg-sec at pH 6.8. The Ca uptake activities were also examined using glycerol-extracted cardiac muscle fibers. Cardiac SR, 1.7 mg/ml, reduced the tension of maximally contracted cardiac muscle fibers to a level corresponding to about 30% of maximum tension, but in the presence of 14.3 mg/ml of mitochondria the maximum tensions of both skeletal muscle and cardiac muscle fibers were maintained for at least 3 min. From these results the time course of relaxation of cardiac muscle induced by cardiac SR or mitochondria was calculated. It was concluded that, in the physiological contraction of cardiac muscle, the SR plays a major role in controlling intracellular Ca2+ movement; the Ca uptake of mitochondria is relatively insignificant. When the cardiac muscle contracts maximally, SR alone cannot relax the cardiac muscle without the aid of other Ca removing system.
研究了与肌浆网(SR)相比,线粒体在心肌中Ca2+对收缩过程的生理调节中是否起重要作用。采用离心法、双波长分光光度法和微孔过滤法测定了鸡心肌SR和兔心肌线粒体的Ca摄取活性。心肌SR的最大Ca摄取能力通常为50 - 60纳摩尔/毫克蛋白质,表观结合常数为2.0×10(6) M-1。在有限负荷条件下,心肌线粒体在pH 7.4时的表观Ca结合常数为2.4×10(5) M-1,在pH 6.8时为5.9×10(4) M-1。在28 - 29℃存在100μM Ca2+时,心肌SR的估计初始Ca摄取速率为20 - 30纳摩尔Ca/毫克·秒,而线粒体在pH 7.4的有限负荷条件下为4.6纳摩尔Ca/毫克·秒,在pH 6.8的大量负荷条件下为0.64纳摩尔Ca/毫克·秒,后者更接近生理条件。在低Ca2+浓度存在时,心肌SR在3.5×10(-7) M Ca2+时的初始Ca摄取速率为0.5纳摩尔Ca/毫克·秒,而线粒体在pH 7.4时1×10(-6) M Ca2+的大量负荷条件下为0.02纳摩尔Ca/毫克·秒,在pH 6.8时为0.004纳摩尔Ca/毫克·秒。还使用甘油提取的心肌纤维检测了Ca摄取活性。1.7毫克/毫升的心肌SR可将最大收缩的心肌纤维张力降低至约最大张力30%的水平,但在存在14.3毫克/毫升线粒体时,骨骼肌和心肌纤维均可维持最大张力至少3分钟。根据这些结果计算了心肌SR或线粒体诱导的心肌松弛的时间进程。得出的结论是,在心肌的生理收缩中,SR在控制细胞内Ca2+运动中起主要作用;线粒体的Ca摄取相对不重要。当心肌最大收缩时,若无其他Ca清除系统的帮助,仅SR无法使心肌松弛。