Skeletal muscle adaptation: training twice every second day vs. training once daily

被引:188
作者
Hansen, AK
Fischer, CP
Plomgaard, P
Andersen, JL
Saltin, B
Pedersen, BK
机构
[1] Univ Copenhagen, Rigshosp, Dept Infect Dis, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen, Rigshosp, Copenahgen Muscle Res Ctr, DK-2100 Copenhagen, Denmark
关键词
substrate availablity; 3-hydroxyacyl-CoA dehydrogenase; citrate synthase;
D O I
10.1152/japplphysiol.00163.2004
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Low muscle glycogen content has been demonstrated to enhance transcription of a number of genes involved in training adaptation. These results made us speculate that training at a low muscle glycogen content would enhance training adaptation. We therefore performed a study in which seven healthy untrained men performed knee extensor exercise with one leg trained in a low-glycogen ( Low) protocol and the other leg trained at a high-glycogen ( High) protocol. Both legs were trained equally regarding workload and training amount. On day 1, both legs ( Low and High) were trained for 1 h followed by 2 h of rest at a fasting state, after which one leg ( Low) was trained for an additional 1 h. On day 2, only one leg ( High) trained for 1 h. Days 1 and 2 were repeated for 10 wk. As an effect of training, the increase in maximal workload was identical for the two legs. However, time until exhaustion at 90% was markedly more increased in the Low leg compared with the High leg. Resting muscle glycogen and the activity of the mitochondrial enzyme 3-hydroxyacyl-CoA dehydrogenase increased with training, but only significantly so in Low, whereas citrate synthase activity increased in both Low and High. There was a more pronounced increase in citrate synthase activity when Low was compared with High. In conclusion, the present study suggests that training twice every second day may be superior to daily training.
引用
收藏
页码:93 / 99
页数:7
相关论文
共 51 条
[21]   Reduced glycogen availability is associated with an elevation in HSP72 in contracting human skeletal muscle [J].
Febbraio, MA ;
Steensberg, A ;
Walsh, R ;
Koukoulas, I ;
van Hall, G ;
Saltin, B ;
Pedersen, BK .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 538 (03) :911-917
[22]   Glucose ingestion attenuates interleukin-6 release from contracting skeletal muscle in humans [J].
Febbraio, MA ;
Steensberg, A ;
Keller, C ;
Starkie, RL ;
Nielsen, HB ;
Krustrup, P ;
Ott, P ;
Secher, NH ;
Pedersen, BK .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 549 (02) :607-612
[23]   Forkhead transcription factor FOX01 (FKHR)-dependent induction of PDK4 gene expression in skeletal muscle during energy deprivation [J].
Furuyama, T ;
Kitayama, K ;
Yamashita, H ;
Mori, N .
BIOCHEMICAL JOURNAL, 2003, 375 :365-371
[24]   SIGNIFICANCE OF SKELETAL-MUSCLE OXIDATIVE ENZYME ENHANCEMENT WITH ENDURANCE TRAINING [J].
GOLLNICK, PD ;
SALTIN, B .
CLINICAL PHYSIOLOGY, 1982, 2 (01) :1-12
[25]   Skeletal muscle metabolism during exercise in humans [J].
Hargreaves, M .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2000, 27 (03) :225-228
[26]  
Hargreaves M, 1997, Exerc Sport Sci Rev, V25, P21
[27]   Effects of 3 days of carbohydrate supplementation on muscle glycogen content and utilisation during a 1-h cycling performance [J].
Hawley, JA ;
Palmer, GS ;
Noakes, TD .
EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY AND OCCUPATIONAL PHYSIOLOGY, 1997, 75 (05) :407-412
[28]   Adaptations of skeletal muscle to prolonged, intense endurance training [J].
Hawley, JA .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2002, 29 (03) :218-222
[29]   Muscle enzyme activity in humans: Role of substrate availability and training [J].
Helge, JW ;
Kiens, B .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 272 (05) :R1620-R1624
[30]   BIOCHEMICAL ADAPTATIONS TO ENDURANCE EXERCISE IN MUSCLE [J].
HOLLOSZY, JO ;
BOOTH, FW .
ANNUAL REVIEW OF PHYSIOLOGY, 1976, 38 :273-291