ROS and myokines promote muscle adaptation to exercise

Trends in Endocrinology and Metabolism

Volumn 20, Issue 3, 2009, Pages 95-99

  Scheele, Camilla ^a   Nielsen, Søren ^a   Pedersen, Bente K ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; FOLLISTATIN RELATED PROTEIN; INTERLEUKIN 15; INTERLEUKIN 6; INTERLEUKIN 8; LEUKEMIA INHIBITORY FACTOR; MYOKINE; PROTEIN FOLLISTATIN LIKE 1; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG;

ADAPTATION; ANTIINFLAMMATORY ACTIVITY; ARTICLE; CELL INTERACTION; CYTOKINE PRODUCTION; EXERCISE; HUMAN; METABOLIC REGULATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

ANIMALS; CYTOKINES; EXERCISE; HUMANS; MODELS, BIOLOGICAL; MUSCLE, SKELETAL; REACTIVE OXYGEN SPECIES; SIGNAL TRANSDUCTION;

EID: 62949125375     PISSN: 10432760     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tem.2008.12.002     Document Type: Article

References (50)

1. Leitzmann M.F., et al. Physical activity recommendations and decreased risk of mortality. Arch. Intern. Med. 167 (2007) 2453-2460
2. Olsen R.H., et al. Metabolic responses to reduced daily steps in healthy nonexercising men. J. Am. Med. Assoc. 299 (2008) 1261-1263
3. Timmons J.A., et al. Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy. FASEB J. 19 (2005) 750-760
4. Timmons J.A., et al. Modulation of extracellular matrix genes reflects the magnitude of physiological adaptation to aerobic exercise training in humans. BMC Biol. 3 (2005) 19
5. Gomez-Cabrera M.C., et al. Moderate exercise is an antioxidant, upregulation of antioxidant genes by training. Free Radic. Biol. Med. 44 (2008) 126-131
6. Steensberg A., et al. Nitric oxide production is a proximal signaling event controlling exercise-induced mRNA expression in human skeletal muscle. FASEB J. 21 (2007) 2683-2694
7. Jackson M.J. Reactive oxygen species and redox-regulation of skeletal muscle adaptations to exercise. Philos. Trans. R. Soc. Lond. B Biol. Sci. 360 (2005) 2285-2291
8. Hotamisligil G.S. Inflammation and metabolic disorders. Nature 444 (2006) 860-867
9. Haffner S.M. The metabolic syndrome: inflammation, diabetes mellitus, and cardiovascular disease. Am. J. Cardiol. 97 (2006) 3-11
10. Perry V.H., et al. Systemic infections and inflammation affect chronic neurodegeneration. Nat. Rev. Immunol. 7 (2007) 161-167
11. Pedersen B.K., et al. Muscle-derived interleukin-6: lipolytic, anti-inflammatory and immune regulatory effects. Pflugers Arch. 446 (2003) 9-16
12. Pedersen B.K., et al. Searching for the exercise factor: is IL-6 a candidate? J. Muscle Res. Cell Motil. 24 (2003) 113-119
13. Nielsen A.R., and Pedersen B.K. The biological roles of exercise-induced cytokines: IL-6, IL-8, and IL-15. Appl. Physiol. Nutr. Metab. 32 (2007) 833-839
14. Pedersen B., et al. Role of myokines in exercise and metabolism. J. Appl. Physiol. 103 (2007) 1093-1098
15. Pedersen B.K., and Febbraio M.A. Muscle as an endocrine organ: focus on muscle-derived interleukin-6. Physiol. Rev. 88 (2008) 1379-1406
16. Arthur P.G., et al. Oxidative stress as a therapeutic target during muscle wasting: considering the complex interactions. Curr. Opin. Clin. Nutr. Metab. Care 11 (2008) 408-416
17. Juarez J.C., et al. Superoxide dismutase 1 (SOD1) is essential for H2O2-mediated oxidation and inactivation of phosphatases in growth factor signaling. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 7147-7152
18. Kelly D.P., and Scarpulla R. Transcriptional regulatory circuits controlling mitochondrial biogenesis and function. Genes Dev. 18 (2004) 357-368
19. Handschin C., and Spiegelman B. The role of exercise and PGC1α in inflammation and chronic disease. Nature 454 (2008) 463-469
20. St-Pierre J., et al. Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators. Cell 127 (2006) 397-408
21. Calvo J.A., et al. Muscle-specific expression of PPARγ coactivator-1α improves exercise performance and increases peak oxygen uptake. J. Appl. Physiol. 104 (2008) 1304-1312
22. Baar K., et al. Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1. FASEB J. 16 (2002) 1879-1886
23. Pilegaard, H., et al. (2003) Exercise induces transient transcriptional activation of the PGC-1α gene in human skeletal muscle. J Physiol.2002.030437 546, 851-858
24. Russell A.P., 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 52 (2003) 2874-2881
25. Haddad F., et al. Pretranslational markers of contractile protein expression in human skeletal muscle: effect of limb unloading plus resistance exercise. J. Appl. Physiol. 98 (2005) 46-52
26. Fredriksson K., et al. Dysregulation of mitochondrial dynamics and the muscle transcriptome in ICU patients suffering from sepsis induced multiple organ failure. PLoS One 3 (2008) e3686
27. Timmons J.A., et al. Expression profiling following local muscle inactivity in humans provides new perspective on diabetes-related genes. Genomics 87 (2006) 165-172
28. Vassilakopoulos T., et al. Antioxidants attenuate the plasma cytokine response to exercise in humans. J. Appl. Physiol. 94 (2003) 1025-1032
29. Fischer C.P., et al. Supplementation with vitamins C and E inhibits the release of interleukin-6 from contracting human skeletal muscle. J. Physiol. 558 (2004) 633-645
30. Ostrowski K., et al. Evidence that interleukin-6 is produced in human skeletal muscle during prolonged running. J. Physiol. 508 (1998) 949-953
31. Carey A.L., et al. Interleukin-6 increases insulin-stimulated glucose disposal in humans and glucose uptake and fatty acid oxidation in vitro via AMP-activated protein kinase. Diabetes 55 (2006) 2688-2697
32. Glund S., et al. Interleukin-6 directly increases glucose metabolism in resting human skeletal muscle. Diabetes 56 (2007) 1630-1637
33. 2+-dependent mechanisms. Am. J. Physiol. Cell Physiol. 293 (2007) C1139-C1147
34. Kelly M., et al. AMPK activity is diminished in tissues of IL-6 knockout mice: the effect of exercise. Biochem. Biophys. Res. Commun. 320 (2004) 449-454
35. Serrano A.L., et al. Interleukin-6 Is an essential regulator of satellite cell-mediated skeletal muscle hypertrophy. Cell Metab. 7 (2008) 33-44
36. Broholm C., et al. Exercise induces expression of leukemia inhibitory factor (LIF) in human skeletal muscle. J. Physiol. 586 (2008) 2195-2201
37. Spangenburg E., and Booth F. Multiple signaling pathways mediate LIF-induced skeletal muscle satellite cell proliferation. Am. J. Physiol. Cell Physiol. 283 (2002) C204-C211
38. Grabstein K.H., et al. Cloning of a T cell growth factor that interacts with the beta chain of the interleukin-2 receptor. Science 264 (1994) 965-968
39. Nielsen A.R., et al. Expression of interleukin-15 in human skeletal muscle effect of exercise and muscle fibre type composition. J. Physiol. 584 (2007) 305-312
40. Bloor C.M. Angiogenesis during exercise and training. Angiogenesis 8 (2005) 263-271
41. Brat D., et al. The role of interleukin-8 and its receptors in gliomagenesis and tumoral angiogenesis. Neural. Oncol. 7 (2005) 122
42. Akerstrom T., et al. Exercise induces interleukin-8 expression in human skeletal muscle. J. Physiol. 563 (2005) 507-516
43. Frydelund-Larsen L., et al. Exercise induces interleukin-8 receptor (CXCR2) expression in human skeletal muscle. Exp. Physiol. 92 (2007) 233-240
44. Ouchi N., et al. Follistatin-like 1, a secreted muscle protein, promotes endothelial cell function and revascularization in ischemic tissue through a nitric oxide synthesis-dependent mechanism. J. Biol. Chem. 283 (2008) 32802-32811
45. Vivekananthan D.P., et al. Use of antioxidant vitamins for the prevention of cardiovascular disease: meta-analysis of randomised trials. Lancet 361 (2003) 2017-2023
46. Jonsdottir I.H., et al. Muscle contractions induce interleukin-6 mRNA production in rat skeletal muscles. J. Physiol. 528 (2000) 157-163
47. Febbraio M.A., and Pedersen B.K. Contraction-induced myokine production and release: is skeletal muscle an endocrine organ? Exerc. Sport Sci. Rev. 33 (2005) 114-119
48. Reid M.B. Free radicals and muscle fatigue: of ROS, canaries, and the IOC. Free Radic. Biol. Med. 44 (2008) 169-179
49. Powers S.K., and Jackson M.J. Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiol. Rev. 88 (2008) 1243-1276
50. Moylan J.S., and Reid M.B. Oxidative stress, chronic disease, and muscle wasting. Muscle Nerve 35 (2007) 411-429