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逐渐降低氧气输送对收缩骨骼肌细胞内稳态的影响。

Effect of gradual reduction in O2 delivery on intracellular homeostasis in contracting skeletal muscle.

作者信息

Hogan M C, Kurdak S S, Arthur P G

机构信息

Department of Medicine, University of California, San Diego, La Jolla 92093-0623, USA.

出版信息

J Appl Physiol (1985). 1996 Apr;80(4):1313-21. doi: 10.1152/jappl.1996.80.4.1313.

Abstract

This study was designed to investigate 1) whether a protocol employing a gradual reduction in O2 availability to submaximally contracting muscle results in relatively minor disturbances in intracellular homeostasis and 2) the interaction between tissue oxygenation and the proposed regulators of muscle respiration, metabolism, and force production. O2 delivery to isolated submaximally contracting [isometric contractions at 3 Hz; approximately 50% of peak O2 uptake (VO2)] in situ canine gastrocnemius (n = 6) was manipulated by decreasing arterial PO2 (hypoxemia; H) or muscle blood flow (ischemia; I) during three separate periods in each muscle [control (C), H, or I; each separated by 45 min of rest]. O2 delivery was reduced gradually in small steps every 3 min by H or I during two of the contraction periods (6 steps for a total of 21 min; O2 delivery reduced by 67% by the end of 21 min), whereas C was at normal O2 delivery for a 15-min period. Muscle VO2 was maintained at control levels for the first two O2 delivery reduction steps for the H and I conditions and then fell proportionally with O2 delivery to approximately 35% of the initial value by the end of the 21-min contraction period. Muscle force development generally fell in parallel with VO2. There was no significant changes from the values obtained during C contractions in intracellular concentrations of ATP, phosphocreatine, NH3, calculated free ADP, lactate, and redox state ratios as the O2 delivery was reduced, even with the severe decline in VO2 and developed force. These results demonstrated that when O2 availability was reduced gradually to contracting skeletal muscle, 1) developed force (ATP utilization) was reduced through a tight coupling with aerobic ATP supply, such that there was little additional disruption of intracellular homeostasis, and 2) there was an apparent dissociation of some of the proposed regulators of cell respiration and force development from the control of these processes.

摘要

本研究旨在调查

1)采用逐渐降低向次最大收缩肌肉输送氧气的方案是否会导致细胞内稳态相对较小的紊乱;2)组织氧合与所提出的肌肉呼吸、代谢和力量产生调节因子之间的相互作用。在每块肌肉的三个不同时间段内,通过降低动脉血氧分压(低氧血症;H)或肌肉血流量(缺血;I)来控制向离体的次最大收缩[3 Hz等长收缩;约为峰值摄氧量(VO2)的50%]的原位犬腓肠肌(n = 6)输送氧气的情况[对照(C)、H或I;每个时间段之间休息45分钟]。在两个收缩期内,通过H或I每3分钟小步逐渐降低氧气输送量(共6步,持续21分钟;到21分钟结束时氧气输送量降低67%),而C在15分钟内保持正常氧气输送量。在H和I条件下,在前两个降低氧气输送量步骤中,肌肉VO2维持在对照水平,然后在21分钟收缩期结束时与氧气输送量成比例下降至初始值的约35%。肌肉力量发展通常与VO2平行下降。随着氧气输送量降低,即使VO2和发展力量严重下降,细胞内ATP、磷酸肌酸、NH3、计算得出的游离ADP、乳酸和氧化还原状态比值与C收缩期获得的值相比也没有显著变化。这些结果表明,当逐渐降低向收缩的骨骼肌输送氧气时:1)发展力量(ATP利用)通过与有氧ATP供应紧密耦合而降低,因此细胞内稳态几乎没有额外的破坏;2)一些所提出的细胞呼吸和力量发展调节因子与这些过程的控制之间存在明显的分离。

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