Determinants of maximal whole-body fat oxidation in elite cross-country skiers: Role of skeletal muscle mitochondria

被引:33
|
作者
Dandanell, Sune [1 ,2 ]
Meinild-Lundby, Anne-Kristine [1 ]
Andersen, Andreas B. [1 ]
Lang, Paul F. [1 ]
Oberholzer, Laura [1 ]
Keiser, Stefanie [1 ]
Robach, Paul [3 ]
Larsen, Steen [2 ]
Ronnestad, Bent R. [4 ]
Lundby, Carsten [1 ]
机构
[1] Univ Zurich, Inst Physiol, Zurich, Switzerland
[2] Univ Copenhagen, Dept Biomed Sci, Ctr Hlth Aging, XLab, Copenhagen, Denmark
[3] Site Ecole Natl Ski & Alpinisme, Ecole Natl Sports Montagne, Chamonix Mt Blanc, France
[4] Innland Univ Appl Sci, Lillehammer, Norway
关键词
cross-country skiing; endurance training; intrinsic mitochondrial function; mitochondrial fat oxidation; mitochondrial volume density; AEROBIC FITNESS; EXERCISE; INTENSITY; MEN; CAPACITY; WOMEN; RATES; ULTRASTRUCTURE; RESPIRATION; PERFORMANCE;
D O I
10.1111/sms.13298
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
Elite endurance athletes possess a high capacity for whole-body maximal fat oxidation (MFO). The aim was to investigate the determinants of a high MFO in endurance athletes. The hypotheses were that augmented MFO in endurance athletes is related to concomitantly increments of skeletal muscle mitochondrial volume density (Mito(VD)) and mitochondrial fatty acid oxidation (FAO(p)), that is, quantitative mitochondrial adaptations as well as intrinsic FAO(p) per mitochondria, that is, qualitative adaptations. Eight competitive male cross-country skiers and eight untrained controls were compared in the study. A graded exercise test was performed to determine MFO, the intensity where MFO occurs (Fat(Max)), and VO2Max. Skeletal muscle biopsies were obtained to determine Mito(VD) (electron microscopy), FAO(p), and OXPHOSp (high-resolution respirometry). The following were higher (P < 0.05) in endurance athletes compared to controls: MFO (mean [95% confidence intervals]) (0.60 g/min [0.50-0.70] vs 0.32 [0.24-0.39]), Fat(Max) (46% VO2Max [44-47] vs 35 [34-37]), VO2Max (71 mL/min/kg [69-72] vs 48 [47-49]), Mito(VD) (7.8% [7.2-8.5] vs 6.0 [5.3-6.8]), FAO(p) (34 pmol/s/mg muscle ww [27-40] vs 21 [17-25]), and OXPHOSp (108 pmol/s/mg muscle ww [104-112] vs 69 [68-71]). Intrinsic FAO(p) (4.0 pmol/s/mg muscle w.w/Mito(VD) [2.7-5.3] vs 3.3 [2.7-3.9]) and OXPHOSp (14 pmol/s/mg muscle ww/Mito(VD) [13-15] vs 11 [10-13]) were, however, similar in the endurance athletes and untrained controls. MFO and Mito(VD) correlated (r(2) = 0.504, P < 0.05) in the endurance athletes. A strong correlation between Mito(VD) and MFO suggests that expansion of Mito(VD) might be rate-limiting for MFO in the endurance athletes. In contrast, intrinsic mitochondrial changes were not associated with augmented MFO.
引用
收藏
页码:2494 / 2504
页数:11
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