Shulman R G, Rothman D L
Departments of Molecular Biophysics and Biochemistry and Diagnostic Radiology, Yale University School of Medicine, New Haven, CT 06510, USA.
Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):457-61. doi: 10.1073/pnas.98.2.457.
Stimulated by recent (13)C and (31)P NMR studies of exercising muscle, we propose a model of the energetics of contraction. Previous studies of energetics have followed energy consumption. However, the rapidity of contraction, in 10-40 msec, requires that energy be delivered rapidly, so that the muscle has power requirements of rapid energy expenditure that are ultimately met by the slower averaged consumption of carbon and oxygen from blood. We propose that energy is supplied in milliseconds by glycogenolysis and that between contractions, glycogenesis refills the pools. The energy for glycogenesis is supplied by oxidative phosphorylation. This mechanism utilizes the rapid conversion of glycogen phosphorylase, the "fight-or-flight" enzyme, to its active form. Lactate is necessarily generated by this pathway to serve as a time buffer between fast and slow energy needs, which resolves the paradoxical generation of lactate in well oxygenated tissue. Consequences of the glycogen shunt are compatible with numerous biochemical and physiological experiments. The model provides a possible mechanism for muscle fatigue, suggesting that at low but nonzero glycogen concentrations, there is not enough glycogen to supply millisecond energy needs.
受近期对运动肌肉的¹³C和³¹P核磁共振研究的启发,我们提出了一个收缩能量学模型。先前的能量学研究关注的是能量消耗。然而,收缩过程在10 - 40毫秒内迅速发生,这就要求能量快速供应,以至于肌肉对能量快速消耗有功率需求,而这最终由血液中碳和氧较慢的平均消耗来满足。我们提出能量在数毫秒内由糖原分解供应,并且在收缩之间,糖原合成会补充糖原储备。糖原合成的能量由氧化磷酸化提供。这种机制利用了糖原磷酸化酶(“应急”酶)迅速转化为其活性形式。该途径必然会产生乳酸,以作为快速和缓慢能量需求之间的时间缓冲,这解决了在充分氧合的组织中乳酸产生的矛盾现象。糖原分流的结果与众多生化和生理学实验相符。该模型为肌肉疲劳提供了一种可能的机制,表明在低但非零的糖原浓度下,没有足够的糖原供应毫秒级的能量需求。