Hypoxia refines plasticity of mitochondrial respiration to repeated muscle work

被引:30
|
作者
Desplanches, Dominique [1 ]
Amami, Myriam [2 ]
Dupre-Aucouturier, Sylvie [1 ]
Valdivieso, Paola [3 ]
Schmutz, Silvia [4 ]
Mueller, Matthias [4 ]
Hoppeler, Hans [4 ]
Kreis, Roland [5 ]
Flueck, Martin [2 ,3 ]
机构
[1] Univ Lyon 1, CNRS, Ctr Genet & Physiol Mol & Cellulaire, UMR 5534, F-69622 Villeurbanne, France
[2] Manchester Metropolitan Univ, Inst Biomed Res Human Movement & Hlth, Manchester M15 6BH, Lancs, England
[3] Univ Zurich, Balgrist Univ Hosp, Dept Orthopaed, Lab Muscle Plast, CH-8008 Zurich, Switzerland
[4] Univ Bern, Inst Anat, Bern, Switzerland
[5] Univ Bern, Dept Clin Res, Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Exercise; Oxygen; Metabolism; Plasticity; Cytochrome c; Gene; HUMAN SKELETAL-MUSCLE; MAXIMAL OXYGEN-UPTAKE; NORMOBARIC HYPOXIA; ENDURANCE RUNNERS; EXERCISE; GENE; EXPRESSION; DESATURATION; CONTRACTILE; EFFICIENCY;
D O I
10.1007/s00421-013-2783-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Purpose We explored whether altered expression of factors tuning mitochondrial metabolism contributes to muscular adaptations with endurance training in the condition of lowered ambient oxygen concentration (hypoxia) and whether these adaptations relate to oxygen transfer as reflected by subsarcolemmal mitochondria and oxygen metabolism in muscle. Methods Male volunteers completed 30 bicycle exercise sessions in normoxia or normobaric hypoxia (4,000 m above sea level) at 65 % of the respective peak aerobic power output. Myoglobin content, basal oxygen consumption, and re-oxygenation rates upon reperfusion after 8 min of arterial occlusion were measured in vastus muscles by magnetic resonance spectroscopy. Biopsies from vastus lateralis muscle, collected pre and post a single exercise bout, and training, were assessed for levels of transcripts and proteins being associated with mitochondrial metabolism. Results Hypoxia specifically lowered the training-induced expression of markers of respiratory complex II and IV (i.e. SDHA and isoform 1 of COX-4; COX4I1) and preserved fibre cross-sectional area. Concomitantly, trends (p < 0.10) were found for a hypoxia-specific reduction in the basal oxygen consumption rate, and improvements in oxygen repletion, and aerobic performance in hypoxia. Repeated exercise in hypoxia promoted the biogenesis of subsarcolemmal mitochondria and this was co-related to expression of isoform 2 of COX-4 with higher oxygen affinity after single exercise, de-oxygenation time and myoglobin content (r >= 0.75). Conversely, expression in COX4I1 with training correlated negatively with changes of subsarcolemmal mitochondria (r < -0.82). Conclusion Hypoxia-modulated adjustments of aerobic performance with repeated muscle work are reflected by expressional adaptations within the respiratory chain and modified muscle oxygen metabolism.
引用
收藏
页码:405 / 417
页数:13
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