Korzeniewski Bernard, Zoladz Jerzy A
Faculty of Biotechnology, Jagiellonian University, ul. Gronostajowa 7, 30-387 Kraków, Poland.
Biophys Chem. 2005 Jul 1;116(2):129-36. doi: 10.1016/j.bpc.2005.03.004. Epub 2005 Apr 21.
It has been proposed recently that the phosphocreatine (PCr) overshoot (increase above the resting level) during muscle recovery after exercise is caused by a slow decay during this recovery of the direct activation of oxidative phosphorylation taking place during muscle work. In the present article the factors determining the appearance and size of the PCr overshoot are studied using the computer model of oxidative phosphorylation in intact skeletal muscle developed previously. It is demonstrated that the appearance and duration of this overshoot is positively correlated with the value of the characteristic decay time of the direct activation of oxidative phosphorylation. It is also shown that the size of PCr overshoot is increased by low resting PCr/Cr ratio (what is confirmed by our unpublished experimental data), by high intensity of the direct activation of oxidative phosphorylation, by high muscle work intensity and by low rate of the return of cytosolic pH to the resting value during muscle recovery.
最近有人提出,运动后肌肉恢复期间磷酸肌酸(PCr)超量(高于静息水平的增加)是由肌肉工作期间发生的氧化磷酸化直接激活在恢复过程中的缓慢衰减引起的。在本文中,使用先前开发的完整骨骼肌氧化磷酸化计算机模型研究了决定PCr超量出现和大小的因素。结果表明,这种超量的出现和持续时间与氧化磷酸化直接激活的特征衰减时间值呈正相关。还表明,低静息PCr/Cr比值(我们未发表的实验数据证实了这一点)、氧化磷酸化直接激活的高强度、高肌肉工作强度以及肌肉恢复期间胞质pH恢复到静息值的低速率会增加PCr超量的大小。