冲刺
间歇训练
高强度间歇训练
最大VO2
强度(物理)
乳酸阈
动物科学
运动处方
自行车
医学
物理疗法
内科学
心脏病学
血乳酸
心率
血压
物理
生物
量子力学
历史
考古
作者
Erin Calaine Inglis,Danilo Iannetta,Letizia Rasica,Mary Z. Mackie,Daniel A. Keir,Martin J. MacInnis,Juan M. Murias
标识
DOI:10.1249/mss.0000000000003406
摘要
ABSTRACT Introduction This study assessed the effect of individualized, domain-based exercise intensity prescription on changes in maximal oxygen uptake (V̇O 2max ) and submaximal thresholds. Methods Eighty-four young healthy participants (42 Females, 42 Males) were randomly assigned to six age, sex, and V̇O 2max -matched groups (14 participants each). Groups performed continuous cycling in the 1) moderate (MOD)-, 2) lower heavy (HVY1)-, and 3) upper heavy-intensity (HVY2)- domain; interval cycling, in the form of 4) high-intensity interval training (HIIT) in the severe-intensity domain, or 5) sprint-interval training (SIT) in the extreme-intensity domain; or no exercise for, 6) control (CON). All training groups except SIT, were work-matched. Training participants completed three sessions per week for six weeks with physiological evaluations performed at PRE, MID and POST intervention. Results Compared to the change in V̇O 2max (∆V̇O 2max ) in CON (0.1 ± 1.2 mL·kg -1 ·min -1 ), all training groups except MOD (1.8 ± 2.7 mL·kg -1 ·min -1 ), demonstrated a significant increase (p < 0.05). HIIT produced the highest increase (6.2 ± 2.8 mL·kg -1 ·min -1 ) followed by HVY2 (5.4 ± 2.3 mL·kg -1 ·min -1 ), SIT (4.7 ± 2.3 mL·kg -1 ·min -1 ), and HVY1 (3.3 ± 2.4 mL·kg -1 ·min -1 ), respectively. The Δ PO at the estimated lactate threshold (θ LT ) was similar across HVY1, HVY2, HIIT and SIT which were all greater than CON (p < 0.05). The Δ V̇O 2 and Δ PO at θ LT for MOD was not different from CON (p > 0.05). HIIT produced the highest Δ PO at maximal metabolic steady state, which was greater than CON, MOD, and SIT (p < 0.05). Conclusions This study demonstrated that i) exercise intensity is a key component determining changes in V̇O 2max and submaximal thresholds and ii) exercise intensity domain-based prescription allows for a homogenous metabolic stimulus across individuals.
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