Bloch G, Chase J R, Meyer D B, Avison M J, Shulman G I, Shulman R G
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06510.
Am J Physiol. 1994 Jan;266(1 Pt 1):E85-91. doi: 10.1152/ajpendo.1994.266.1.E85.
Time courses of the glycogen synthesis rate and of the glucose 6-phosphate (G-6-P) concentration after an electrically induced exercise were followed in the anesthetized rat gastrocnemius by in vivo 13C and 31P nuclear magnetic resonance (NMR) spectroscopy, respectively. The ratio of glycogen synthase I to glycogen synthase I and D (I/I+D) and allosteric activation by G-6-P were also studied in vitro on muscles sampled at rest and 10 min (early recovery) and 100 min (late recovery) after exercise. From early recovery to late recovery, the in vivo glycogen synthesis rate dropped from 0.46 +/- 0.06 to 0.11 +/- 0.04 mmol.kg wet tissue-1.min-1, the G-6-P concentration from 0.83 +/- 0.08 to 0.32 +/- 0.05 mmol/kg wet tissue, and I/I+D from 83 +/- 4 to 47 +/- 1%. The combination of the changes in G-6-P concentration and in I/I+D quantitatively describes the fourfold decrease in glycogen synthesis rate from early to late recovery. These results demonstrate that phosphorylation, determining glycogen synthase I/I+D, and allosteric control of glycogen synthase by G-6-P contribute approximately equally to the regulation of the postexercise in vivo glycogen synthesis rate.
分别通过体内¹³C和³¹P核磁共振(NMR)光谱法,追踪麻醉大鼠腓肠肌在电刺激运动后糖原合成速率和6-磷酸葡萄糖(G-6-P)浓度的时间进程。还在体外研究了运动后静息时、10分钟(早期恢复)和100分钟(晚期恢复)采集的肌肉中糖原合酶I与糖原合酶I和D(I/I+D)的比例以及G-6-P的变构激活作用。从早期恢复到晚期恢复,体内糖原合成速率从0.46±0.06降至0.11±0.04 mmol·kg湿组织⁻¹·min⁻¹,G-6-P浓度从0.83±0.08降至0.32±0.05 mmol/kg湿组织,I/I+D从83±4降至47±1%。G-6-P浓度和I/I+D的变化相结合,定量描述了从早期恢复到晚期恢复糖原合成速率降低四倍的情况。这些结果表明,决定糖原合酶I/I+D的磷酸化作用以及G-6-P对糖原合酶的变构控制,对运动后体内糖原合成速率的调节作用大致相同。