Biochemical origin of (near-) linear curvature constant (W')- V ˙ O 2 slow component ( Δ V ˙ O 2 sc ) and critical power (CP)- V ˙ O 2 transition time (t0.63) relationship in skeletal muscle.

IF 2.8 3区 医学 Q2 PHYSIOLOGY
Bernard Korzeniewski
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引用次数: 0

Abstract

Purpose: The biochemical background of the (near-)linear direct relationship between the curvature constant (W') of the power-duration curve and the magnitude ( Δ V ˙ O 2sc ) of the slow component of the V ˙ O 2 on-kinetics ( V ˙ O 2sc ) as well as reverse relationship between critical power (CP) and the characteristic transition time (t0.63, analogous to τp) of the primary phase II of the V ˙ O 2 on-kinetics encountered in experimental studies is studied.

Methods: A computer model of the bioenergetic system in skeletal muscle, involving the each-step-activation mechanism of work transitions and Pi double-threshold mechanism of muscle fatigue, is used.

Results: The activity (rate constant) (kadd) of the additional ATP usage, underlying the slow component, determines to a large extent the (near-)linear direct W'- Δ V ˙ O 2sc relationship, as an increase in kadd increases markedly both W' and Δ V ˙ O 2sc . t0.63 is a derivative of the changes in metabolite (M = PCr or Cr or Pi) concentrations between rest and the steady-state of the phase II M on-kinetics after the onset of exercise. The oxidative phosphorylation (OXPHOS) activity (kOX) mostly determines the (near)-linear inverse CP-t0.63 relationship, as an increase in kOX markedly decreases ΔM and t0.63, and elevates CP.

Conclusions: The V ˙ O 2 on-kinetics (e.g., V ˙ O 2sc or t0.63) cannot cause anything in the system, as it is an emergent property of the system functioning on the biochemical level. Physiological variables: muscle V ˙ O 2sc and W' as well as t0.63 and CP, and relationships between them, are determined by biochemical parameters, mainly kadd and kOX, respectively.

骨骼肌(近)线性曲率常数(W')- V ˙ O 2 慢分量(Δ V ˙ O 2 sc)和临界功率(CP)- V ˙ O 2 过渡时间(t0.63)关系的生化起源。
目的:研究功率-持续时间曲线的曲率常数(W')与 V ˙ O 2 动力学慢分量(V ˙ O 2sc)的大小(Δ V ˙ O 2sc)之间(近似)线性直接关系的生化背景,以及临界功率(CP)与实验研究中遇到的 V ˙ O 2 动力学第一阶段 II 的特征转换时间(t0.63,类似于τp)的反向关系:方法:使用骨骼肌生物能系统的计算机模型,其中涉及工作转换的每一步激活机制和肌肉疲劳的 Pi 双阈机制:结果:作为慢速成分的基础,额外 ATP 使用的活性(速率常数)(kadd)在很大程度上决定了 W'- Δ V ˙ O 2sc 的(近)线性直接关系,因为 kadd 的增加会显著增加 W' 和 Δ V ˙ O 2sc。t0.63 是代谢物(M = PCr、Cr 或 Pi)浓度从静止到运动开始后第二阶段 M 动力学稳态之间变化的导数。氧化磷酸化(OXPHOS)活性(kOX)在很大程度上决定了 CP-t0.63 的(近)线性反比关系,因为 kOX 的增加会显著降低 ΔM 和 t0.63,并提高 CP:结论:V˙O 2 动力学(如 V ˙ O 2sc 或 t0.63)不会对系统造成任何影响,因为它是系统在生化水平上运作的一个显现属性。生理变量:肌肉 V ˙ O 2sc 和 W'以及 t0.63 和 CP 以及它们之间的关系分别由生化参数(主要是 kadd 和 kOX)决定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
6.70%
发文量
227
审稿时长
3 months
期刊介绍: The European Journal of Applied Physiology (EJAP) aims to promote mechanistic advances in human integrative and translational physiology. Physiology is viewed broadly, having overlapping context with related disciplines such as biomechanics, biochemistry, endocrinology, ergonomics, immunology, motor control, and nutrition. EJAP welcomes studies dealing with physical exercise, training and performance. Studies addressing physiological mechanisms are preferred over descriptive studies. Papers dealing with animal models or pathophysiological conditions are not excluded from consideration, but must be clearly relevant to human physiology.
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