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Whole body and leg acetate kinetics at rest, during exercise and recovery in humans

机译:人体静止,运动和恢复期间的全身和腿部乙酸盐动力学

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摘要

We have used a constant [1,2-13C]acetate infusion (0.12 μmol min−1 kg1) for 2 h at rest, followed by 2 h of one-legged knee-extensor exercise at 65 % of leg maximal workload, and 3 h of recovery in six post-absorptive volunteers to quantify whole-body and leg acetate kinetics and determine whether the whole-body acetate correction factor can be used to correct leg substrate oxidation. The acetate whole-body rate of appearance (Ra) was not significantly different at rest, during exercise or during recovery (365-415 μmol min−1). The leg net acetate uptake was similar at rest and during recovery (≈10 μmol min−1), but increased ∼5-fold with exercise. At rest the leg acetate uptake (≈15 μmol min−1) and release (≈5 μmol min−1) accounted for 4 and 1.5 % of whole-body acetate disposal (Rd) and Ra, respectively. When the leg acetate kinetics were extrapolated to the total body skeletal muscle mass, then skeletal muscle accounted for ∼16 and ∼6 % of acetate Rd and Ra. With exercise, leg acetate uptake increased ∼6-fold, whereas leg acetate release increased 9-fold compared with rest. Whole-body acetate carbon recovery increased with time of infusion at rest and during recovery from 21 % after 1.5 h of infusion to 45 % in recovery after 7 h of infusion. Leg and whole-body acetate carbon recovery were similar under resting conditions, both before and after exercise. During exercise whole-body acetate carbon recovery was ∼75 %, however, acetate carbon recovery of the active leg was substantially higher (≈100 %). It is concluded that inactive skeletal muscle plays a minor role in acetate turnover. However, active skeletal muscle enhances several-fold acetate uptake and subsequent oxidation, as well as release and its contribution to whole-body acetate turnover. Furthermore, under resting conditions the whole-body acetate correction factor can be used to correct for leg, skeletal muscle, substrate oxidation, but not during exercise.
机译:我们在休息状态下连续2小时使用恒定的[1,2-13C]乙酸酯输注(0.12μmolmin-1 kg1),然后在腿部最大负重65%的情况下进行2小时单腿伸膝运动,而3在六名吸收后志愿者中恢复的小时数,以量化全身和腿部乙酸盐的动力学,并确定全身乙酸盐校正因子是否可用于校正腿底物的氧化。休息,运动或恢复期间(365-415μmolmin-1)的乙酸盐全身出现率(Ra)均无显着差异。腿部净乙酸盐的摄取在休息时和恢复期间相似(≈10μmolmin-1),但随着运动增加约5倍。静息时,腿部乙酸盐的摄取(≈15μmolmin-1)和释放(≈5μmolmin-1)分别占全身乙酸盐处置量(Rd)和Ra的4%和1.5%。当腿部乙酸盐动力学被外推至全身骨骼肌质量时,骨骼肌占乙酸盐Rd和Ra的约16%和约6%。运动后,腿部醋酸盐的摄取增加了约6倍,而腿部醋酸盐的释放则增加了9倍。全身醋酸盐碳的回收率随静息时间和输注时间的增加而增加,从输注1.5小时后的21%增加到输注7小时后的恢复的45%。运动前和运动后,腿部和全身乙酸盐的碳回收在静止条件下均相似。在运动过程中,全身乙酸盐的碳回收率为〜75%,但是活动腿的乙酸盐的碳回收率则更高(≈100%)。结论是,骨骼肌无活性在乙酸盐转换中起次要作用。然而,活跃的骨骼肌会增加几倍的乙酸盐吸收和随后的氧化,以及释放及其对全身乙酸盐更新的贡献。此外,在休息条件下,全身醋酸盐校正因子可用于校正腿部,骨骼肌,底物氧化,但不适用于运动期间。

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