Wilkinson Sarah B, Kim Paul L, Armstrong David, Phillips Stuart M
Exercise Metabolism Research Group, Department of Kinesiology, McMaster University, 1280 Main St. West, Hamilton, ON L8S 4K1, Canada.
Appl Physiol Nutr Metab. 2006 Oct;31(5):518-29. doi: 10.1139/h06-028.
We examined the effect of a post-exercise oral carbohydrate (CHO, 1 g.kg(-1).h(-1)) and essential amino acid (EAA, 9.25 g) solution containing glutamine (0.3 g/kg BW; GLN trial) versus an isoenergetic CHO-EAA solution without glutamine (control, CON trial) on muscle glycogen resynthesis and whole-body protein turnover following 90 min of cycling at 65% VO2 peak. Over the course of 3 h of recovery, muscle biopsies were taken to measure glycogen resynthesis and mixed muscle protein synthesis (MPS), by incorporation of [ring-2H5] phenylalanine. Infusion of [1-13C] leucine was used to measure whole-body protein turnover. Exercise resulted in a significant decrease in muscle glycogen (p < 0.05) with similar declines in each trial. Glycogen resynthesis following 3 h of recovery indicated no difference in total accumulation or rate of repletion. Leucine oxidation increased 2.5 fold (p < 0.05) during exercise, returned to resting levels immediately post-exercise,and was again elevated at 3 h post-exercise (p < 0.05). Leucine flux, an index of whole-body protein breakdown rate, was reduced during exercise, but increased to resting levels immediately post-exercise, and was further increased at 3 h post-exercise (p < 0.05), but only during the CON trial. Exercise resulted in a marked suppression of whole-body protein synthesis (50% of rest; p < 0.05), which was restored post-exercise; however, the addition of glutamine did not affect whole-body protein synthesis post-exercise. The rate of MPS was not different between trials. The addition of glutamine to a CHO + EAA beverage had no effect on post-exercise muscle glycogen resynthesis or muscle protein synthesis, but may suppress a rise in whole-body proteolysis during the later stages of recovery.
我们研究了运动后口服含谷氨酰胺的碳水化合物(CHO,1 g·kg⁻¹·h⁻¹)和必需氨基酸(EAA,9.25 g)溶液(谷氨酰胺试验,GLN试验)与不含谷氨酰胺的等能量CHO-EAA溶液(对照组,CON试验)对在65%最大摄氧量下进行90分钟骑行后肌肉糖原再合成及全身蛋白质周转率的影响。在3小时的恢复过程中,通过掺入[环-²H₅]苯丙氨酸进行肌肉活检,以测量糖原再合成和混合肌肉蛋白质合成(MPS)。输注[¹-¹³C]亮氨酸用于测量全身蛋白质周转率。运动导致肌肉糖原显著减少(p < 0.05),各试验中的下降情况相似。恢复3小时后的糖原再合成表明,总积累量或补充速率没有差异。亮氨酸氧化在运动期间增加了2.5倍(p < 0.05),运动后立即恢复到静息水平,并在运动后3小时再次升高(p < 0.05)。亮氨酸通量是全身蛋白质分解率的指标,在运动期间降低,但运动后立即增加到静息水平,并在运动后3小时进一步增加(p < 0.05),但仅在CON试验中如此。运动导致全身蛋白质合成显著抑制(为静息时的50%;p < 0.05),运动后恢复;然而,添加谷氨酰胺对运动后全身蛋白质合成没有影响。试验之间MPS速率没有差异。在CHO + EAA饮料中添加谷氨酰胺对运动后肌肉糖原再合成或肌肉蛋白质合成没有影响,但可能会抑制恢复后期全身蛋白水解的增加。