Whole body metabolic effects of prolonged endurance training in combination with erythropoietin treatment in humans: a randomized placebo controlled trial

被引:30
作者
Christensen, Britt [1 ,2 ,3 ]
Nellemann, Birgitte [1 ,3 ]
Larsen, Mads S. [2 ]
Thams, Line [2 ]
Sieljacks, Peter [2 ]
Vestergaard, Poul F. [1 ,3 ]
Bibby, Bo Martin [4 ]
Vissing, Kristian [2 ]
Stodkilde-Jorgensen, Hans [5 ]
Pedersen, Steen B. [1 ]
Moller, Niels [3 ]
Nielsen, Soren [1 ]
Jessen, Niels [6 ]
Jorgensen, Jens Otto L. [1 ]
机构
[1] Aarhus Univ Hosp, NBG THG, Dept Endocrinol & Internal Med, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Inst Publ Hlth, Sect Sports Sci, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Inst Clin Med, Med Res Labs, DK-8000 Aarhus, Denmark
[4] Univ Aarhus, Dept Biostat, Aarhus, Denmark
[5] Aarhus Univ Hosp, MR Res Ctr, DK-8000 Aarhus, Denmark
[6] Aarhus Univ Hosp, Inst Clin Med, Res Lab Biochem Pathol, DK-8000 Aarhus, Denmark
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2013年 / 305卷 / 07期
关键词
metabolism; resting energy expenditure; insulin sensitivity; body composition; intrahepatic lipid; RECOMBINANT-HUMAN-ERYTHROPOIETIN; HUMAN SKELETAL-MUSCLE; RESTING ENERGY-EXPENDITURE; FATTY-ACID TURNOVER; HEMODIALYSIS-PATIENTS; INSULIN SENSITIVITY; MITOCHONDRIAL BIOGENESIS; RESONANCE-SPECTROSCOPY; LIPID-METABOLISM; AEROBIC FITNESS;
D O I
10.1152/ajpendo.00269.2013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Erythropoietin (Epo) administration improves aerobic exercise capacity and insulin sensitivity in renal patients and also increases resting energy expenditure (REE). Similar effects are observed in response to endurance training. The aim was to compare the effects of endurance training with erythropoiesis-stimulating agent (ESA) treatment in healthy humans. Thirty-six healthy untrained men were randomized to 10 wk of either: 1) placebo (n = 9), 2) ESA (n = 9), 3) endurance training (n = 10), or 4) ESA and endurance training (n = 8). In a single-blinded design, ESA/placebo was injected one time weekly. Training consisted of biking for 1 h at 65% of wattmax three times per week. Measurements performed before and after the intervention were as follows: body composition, maximal oxygen uptake, insulin sensitivity, REE, and palmitate turnover. Uncoupling protein 2 (UCP2) mRNA levels were assessed in skeletal muscle. Fat mass decreased after training (P = 0.003), whereas ESA induced a small but significant increase in intrahepatic fat (P = 0.025). Serum free fatty acid (FFA) levels and palmitate turnover decreased significantly in response to training, whereas the opposite pattern was found after ESA. REE corrected for lean body mass increased in response to ESA and training, and muscle UCP2 mRNA levels increased after ESA (P = 0.035). Insulin sensitivity increased only after training (P = 0.011). In conclusion: 1) insulin sensitivity is not improved after ESA treatment despite improved exercise capacity, 2) the calorigenic effects of ESA may be related to increased UCP2 gene expression in skeletal muscle, and 3) training and ESA exert opposite effects on lipolysis under basal conditions, increased FFA levels and liver fat fraction was observed after ESA treatment.
引用
收藏
页码:E879 / E889
页数:11
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