Burgomaster Kirsten A, Howarth Krista R, Phillips Stuart M, Rakobowchuk Mark, Macdonald Maureen J, McGee Sean L, Gibala Martin J
Exercise Metabolism Research Group, Department of Kinesiology, McMaster University, Hamilton, Ontario, Canada.
J Physiol. 2008 Jan 1;586(1):151-60. doi: 10.1113/jphysiol.2007.142109. Epub 2007 Nov 8.
Low-volume 'sprint' interval training (SIT) stimulates rapid improvements in muscle oxidative capacity that are comparable to levels reached following traditional endurance training (ET) but no study has examined metabolic adaptations during exercise after these different training strategies. We hypothesized that SIT and ET would induce similar adaptations in markers of skeletal muscle carbohydrate (CHO) and lipid metabolism and metabolic control during exercise despite large differences in training volume and time commitment. Active but untrained subjects (23 +/- 1 years) performed a constant-load cycling challenge (1 h at 65% of peak oxygen uptake (.VO(2peak)) before and after 6 weeks of either SIT or ET (n = 5 men and 5 women per group). SIT consisted of four to six repeats of a 30 s 'all out' Wingate Test (mean power output approximately 500 W) with 4.5 min recovery between repeats, 3 days per week. ET consisted of 40-60 min of continuous cycling at a workload that elicited approximately 65% (mean power output approximately 150 W) per day, 5 days per week. Weekly time commitment (approximately 1.5 versus approximately 4.5 h) and total training volume (approximately 225 versus approximately 2250 kJ week(-1)) were substantially lower in SIT versus ET. Despite these differences, both protocols induced similar increases (P < 0.05) in mitochondrial markers for skeletal muscle CHO (pyruvate dehydrogenase E1alpha protein content) and lipid oxidation (3-hydroxyacyl CoA dehydrogenase maximal activity) and protein content of peroxisome proliferator-activated receptor-gamma coactivator-1alpha. Glycogen and phosphocreatine utilization during exercise were reduced after training, and calculated rates of whole-body CHO and lipid oxidation were decreased and increased, respectively, with no differences between groups (all main effects, P < 0.05). Given the markedly lower training volume in the SIT group, these data suggest that high-intensity interval training is a time-efficient strategy to increase skeletal muscle oxidative capacity and induce specific metabolic adaptations during exercise that are comparable to traditional ET.
低容量“冲刺”间歇训练(SIT)能迅速提高肌肉氧化能力,其提升程度与传统耐力训练(ET)相当,但尚无研究探讨这两种不同训练策略后运动期间的代谢适应性变化。我们推测,尽管训练量和时间投入存在巨大差异,但SIT和ET在运动期间骨骼肌碳水化合物(CHO)和脂质代谢标志物以及代谢控制方面会引发相似的适应性变化。活跃但未经训练的受试者(23±1岁)在进行6周的SIT或ET训练(每组5名男性和5名女性)前后,进行了一次恒定负荷的骑行挑战(在峰值摄氧量(.VO₂peak)的65%强度下骑行1小时)。SIT包括进行四到六组30秒的“全力”温盖特测试(平均功率输出约500瓦),每组之间休息4.5分钟,每周训练3天。ET包括每天进行40 - 60分钟的持续骑行,负荷强度约为峰值摄氧量的65%(平均功率输出约150瓦),每周训练5天。与ET相比,SIT的每周时间投入(约1.5小时对约4.5小时)和总训练量(约225千焦/周对约2250千焦/周)显著更低。尽管存在这些差异,但两种训练方案均使骨骼肌CHO(丙酮酸脱氢酶E1α蛋白含量)和脂质氧化(3 - 羟酰基辅酶A脱氢酶最大活性)的线粒体标志物以及过氧化物酶体增殖物激活受体γ共激活因子 - 1α的蛋白含量出现相似程度的增加(P < 0.05)。训练后运动期间糖原和磷酸肌酸的利用率降低,全身CHO和脂质氧化的计算速率分别下降和上升,两组之间无差异(所有主要效应,P < 0.05)。鉴于SIT组的训练量明显更低,这些数据表明高强度间歇训练是一种提高骨骼肌氧化能力并在运动期间诱导与传统ET相当的特定代谢适应性变化的高效策略。