Similar expression of oxidative genes after interval and continuous exercise

Medicine and Science in Sports and Exercise

Volumn 41, Issue 12, 2009, Pages 2136-2144

  Wang, Li ^a,c   Psilander, Niklas ^a,b   Tonkonogi, Michail ^a,d   Ding, Shuzhe ^c   Sahlin, Kent ^a,b,e  

^a SWEDISH SCHOOL OF SPORT AND HEALTH SCIENCES   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c EAST CHINA NORMAL UNIVERSITY   (China)

^d DALARNA UNIVERSITY   (Sweden)

^e UNIVERSITY OF SOUTHERN DENMARK   (Denmark)

Author keywords

Biomarkers; Interval training; Metabolic adaptation; Muscle oxidative potential; Transcriptional regulation

Indexed keywords

ADAPTATION, PHYSIOLOGICAL; ADULT; BASE SEQUENCE; BIOLOGICAL MARKERS; EXERCISE; FEMALE; GENE EXPRESSION REGULATION; GLYCOGEN; HUMANS; LIPID METABOLISM; MALE; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; OXIDATIVE STRESS; OXYGEN CONSUMPTION; POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 73449096390     PISSN: 01959131     EISSN: 15300315     Source Type: Journal    
DOI: 10.1249/MSS.0b013e3181abc1ec     Document Type: Article

References (32)

1. Burgomaster KA, Howarth KR, Phillips SM, et al. Similar metabolic adaptations during exercise after low volume sprint interval and traditional endurance training in humans. J Physiol. 2008;586:151-160
2. Daussin FN, Zoll J, Dufour SP, et al. Effect of interval versus continuous training on cardiorespiratory and mitochondrial functions: relationship to aerobic performance improvements in sedentary subjects. Am J Physiol Regul Integr Comp Physiol. 2008;295:R264-72.
3. Dudley GA, Abraham WM, Terjung RL. Influence of exercise intensity and duration on biochemical adaptations in skeletal muscle. J Appl Physiol. 1982;53:844-850
4. Gibala MJ. High-intensity interval training: a time-efficient strategy for health promotion? Curr Sports Med Rep. 2007;6:211-213
5. Gibala MJ, Little JP, van Essen M, et al. Short-term sprint interval versus traditional endurance training: similar initial adaptations in human skeletal muscle and exercise performance. J Physiol. 2006;575:901-911
6. Gibala MJ, McGee SL, Garnham AP, Howlett KF, Snow RJ, Hargreaves M. Brief intense interval exercise activates AMPK and p38 MAPK signaling and increases the expression of PGC-1{alpha} in human skeletal muscle. J Appl Physiol. 2009;106: 929-934
7. Hashimoto T, Hussien R, Oommen S, Gohil K, Brooks GA. Lactate sensitive transcription factor network in L6 cells: activation of MCT1 and mitochondrial biogenesis. FASEB J. 2007;21:2602-2612
8. Hildebrandt AL, Pilegaard H, Neufer PD. Differential transcrip-tional activation of select metabolic genes in response to variations in exercise intensity and duration. Am J Physiol Endocrinol Metab. 2003;285:E1021-7.
9. Hood DA. Invited Review: contractile activity-induced mito-chondrial biogenesis in skeletal muscle. J Appl Physiol. 2001;90: 1137-1157
10. Jager S, Handschin C, St-Pierre J, Spiegelman BM. AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1alpha. Proc Natl Acad Sci U S A. 2007;104:12017-12022
11. Jucker BM, Yang D, Casey WM, et al. Selective PPARdelta agonist treatment increases skeletal muscle lipid metabolism without altering mitochondrial energy coupling: an in vivo magnetic resonance spectroscopy study. Am J Physiol Endocrinol Metab. 2007;293:E1256-64.
12. Leighton B, Blomstrand E, Challiss RA, et al. Acute and chronic effects of strenuous exercise on glucose metabolism in isolated, incubated soleus muscle of exercise-trained rats. Acta Physiol Scand. 1989;136:177-184 (Pubitemid 19155621)
13. Lin J, Puigserver P, Donovan J, Tarr P, Spiegelman BM. Peroxisome proliferator-activated receptor gamma coactivator 1beta (PGC-1beta), a novel PGC-1-related transcription coac-tivator associated with host cell factor. J Biol Chem. 2002;277: 1645-1648
14. Mahoney DJ, Parise G, Melov S, Safdar A, Tarnopolsky MA. Analysis of global mRNA expression in human skeletal muscle during recovery from endurance exercise. FASEB J. 2005;19: 1498-1500
15. Meirhaeghe A, Crowley V, Lenaghan C, et al. Characterization of the human, mouse and rat PGC1 beta (peroxisome-proliferator-activated receptor-gamma co-activator 1 beta) gene in vitro and in vivo. Biochem J. 2003;373:155-165
16. Mortensen OH, Plomgaard P, Fischer CP, Hansen AK, Pilegaard H, Pedersen BK. PGC-1beta is downregulated by training in human skeletal muscle: no effect of training twice every second day vs. once daily on expression of the PGC-1 family. J Appl Physiol. 2007;103:1536-1542
17. Muoio DM, MacLean PS, Lang DB, et al. Fatty acid homeostasis and induction of lipid regulatory genes in skeletal muscles of peroxisome proliferator-activated receptor (PPAR) alpha knockout mice. Evidence for compensatory regulation by PPAR delta. J Biol Chem. 2002;277:26089-26097
18. Norrbom J, Sundberg CJ, Ameln H, Kraus WE, Jansson E, Gustafsson T. PGC-1alpha mRNA expression is influenced by metabolic perturbation in exercising human skeletal muscle. J Appl Physiol. 2004;96:189-194
19. Pilegaard H, Keller C, Steensberg A, et al. Influence of pre-exercise muscle glycogen content on exercise-induced transcrip-tional regulation of metabolic genes. J Physiol. 2002;541:261-271
20. Pilegaard H, Ordway GA, Saltin B, Neufer PD. Transcriptional regulation of gene expression in human skeletal muscle during recovery from exercise. Am J Physiol Endocrinol Metab. 2000; 279:E806-14.
21. Pilegaard H, Saltin B, Neufer PD. Exercise induces transient transcriptional activation of the PGC-1alpha gene in human skeletal muscle. J Physiol. 2003;546:851-858
22. Rognmo O, Hetland E, Helgerud J, Hoff J, Slordahl SA. High intensity aerobic interval exercise is superior to moderate intensity exercise for increasing aerobic capacity in patients with coronary artery disease. Eur J Cardiovasc Prev Rehabil. 2004;11:216-222
23. Russell AP, Feilchenfeldt J, Schreiber S, et al. Endurance training in humans leads to fiber type-specific increases in levels of peroxisome proliferator-activated receptor-gamma coactivator-1 and peroxisome proliferator-activated receptor-alpha in skeletal muscle. Diabetes. 2003;52:2874-2881
24. Russell AP, Hesselink MK, Lo SK, Schrauwen P. Regulation of metabolic transcriptional co-activators and transcription factors with acute exercise. FASEB J. 2005;19:986-988
25. Scarpulla RC. Transcriptional activators and coactivators in the nuclear control of mitochondrial function in mammalian cells. Gene. 2002;286:81-89
26. Sriwijitkamol A, Coletta DK, Wajcberg E, et al. Effect of acute exercise on AMPK signaling in skeletal muscle of subjects with type 2 diabetes: a time-course and dose-response study. Diabetes. 2007;56:836-848
27. Taylor EB, Lamb JD, Hurst RW, et al. Endurance training increases skeletal muscle LKB1 and PGC-1alpha protein abundance: effects of time and intensity. Am J Physiol Endocrinol Metab. 2005;289:E960-8.
28. Wacker MJ, Tehel MM, Gallagher PM. Technique for quantitative RT-PCR analysis directly from single muscle fibers. J Appl Physiol. 2008;105:308-315
29. Watt MJ, Southgate RJ, Holmes AG, Febbraio MA. Suppression of plasma free fatty acids upregulates peroxisome proliferator-activated receptor (PPAR) alpha and delta and PPAR coactivator 1alpha in human skeletal muscle, but not lipid regulatory genes. J Mol Endocrinol. 2004;33:533-544
30. Wende AR, Huss JM, Schaeffer PJ, Giguere V, Kelly DP. PGC-1alpha coactivates PDK4 gene expression via the orphan nuclear receptor ERRalpha: a mechanism for transcriptional control of muscle glucose metabolism. Mol Cell Biol. 2005;25: 10684-10694
31. Wu Z, Puigserver P, Andersson U, et al. Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1. Cell. 1999;98:115-124
32. Yan Z, Li P, Akimoto T. Transcriptional control of the Pgc-1alpha gene in skeletal muscle in vivo. Exerc Sport Sci Rev. 2007;35:97-101