Interleukin-6 release from human skeletal muscle during exercise: relation to AMPK activity.

We tested the hypothesis that IL-6 release from muscle during exercise may be related to muscle activity of 5'-AMP-activated protein kinase (AMPK). Eight healthy, well-trained young men completed two 60-min trials on a bicycle ergometer at 70% of their peak oxygen uptake in either a glycogen-depleted or a glycogen-loaded state. IL-6 was released from the leg already after 10 min of exercise in the glycogen-depleted state, whereas no significant release was observed at any time in the loaded state. Nevertheless, plasma IL-6 increased similarly in the two trials from approximately 0.8 pg/ml at rest to approximately 4.5 pg/ml after 60 min of exercise. Activity of alpha1-AMPK (160%) and alpha2-AMPK (145%) was increased at rest in the glycogen-depleted compared with the loaded situation. During exercise, alpha1-AMPK activity did not change from resting levels in both trials, whereas alpha2-AMPK activity increased only in the glycogen-depleted state. After 60 min of exercise in the glycogen-depleted state, individual values of alpha2-AMPK activity correlated significantly (r = 0.87, P < 0.006) with individual values of IL-6 release as well as with average IL-6 release over the entire 60 min (r = 0.86, P < 0.006). The present data are compatible with a role for AMPK in IL-6 release during exercise or a role for IL-6 in activating AMPK. Alternatively, both AMPK and IL-6 are independent sensors of a low muscle glycogen concentration during exercise. In addition, leg release of IL-6 cannot alone explain the increase in plasma IL-6 during exercise.

[1]  B. Pedersen,et al.  IL‐6 Gene Expression in Human Adipose Tissue in Response to Exercise – Effect of Carbohydrate Ingestion , 2003, The Journal of physiology.

[2]  B. Saltin,et al.  Interleukin-6 stimulates lipolysis and fat oxidation in humans. , 2003, The Journal of clinical endocrinology and metabolism.

[3]  Y. Hellsten,et al.  Regulation of 5'AMP-activated protein kinase activity and substrate utilization in exercising human skeletal muscle. , 2003, American journal of physiology. Endocrinology and metabolism.

[4]  M. Febbraio,et al.  Acute interleukin‐6 administration does not impair muscle glucose uptake or whole‐body glucose disposal in healthy humans , 2003, The Journal of physiology.

[5]  B. Pedersen,et al.  The effect of graded exercise on IL‐6 release and glucose uptake in human skeletal muscle , 2003, The Journal of physiology.

[6]  M. Febbraio,et al.  Muscle‐derived interleukin‐6: mechanisms for activation and possible biological roles , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  H. Langberg,et al.  Substantial elevation of interleukin‐6 concentration in peritendinous tissue, in contrast to muscle, following prolonged exercise in humans , 2002, The Journal of physiology.

[8]  N. Secher,et al.  Interleukin‐6 release from the human brain during prolonged exercise , 2002, The Journal of physiology.

[9]  Y. Hellsten,et al.  Glycogen-dependent effects of 5-aminoimidazole-4-carboxamide (AICA)-riboside on AMP-activated protein kinase and glycogen synthase activities in rat skeletal muscle. , 2002, Diabetes.

[10]  D. Hardie,et al.  AMP‐activated protein kinase: the energy charge hypothesis revisited , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[11]  B. Saltin,et al.  Interleukin‐6 production in contracting human skeletal muscle is influenced by pre‐exercise muscle glycogen content , 2001, The Journal of physiology.

[12]  P. Neufer,et al.  Transcriptional activation of the IL‐6 gene in human contracting skeletal muscle: influence of muscle glycogen content , 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[13]  A. Steensberg,et al.  Muscle‐derived interleukin‐6: possible biological effects , 2001, The Journal of physiology.

[14]  A. Steensberg,et al.  Plasma interleukin-6 during strenuous exercise: role of epinephrine. , 2001, American journal of physiology. Cell physiology.

[15]  A. Steensberg,et al.  Exercise and cytokines with particular focus on muscle-derived IL-6. , 2001, Exercise immunology review.

[16]  M. Gleeson Interleukins and exercise , 2000, The Journal of physiology.

[17]  B. Saltin,et al.  Production of interleukin‐6 in contracting human skeletal muscles can account for the exercise‐induced increase in plasma interleukin‐6 , 2000, The Journal of physiology.

[18]  B. Hansen,et al.  Isoform‐specific and exercise intensity‐dependent activation of 5′‐AMP‐activated protein kinase in human skeletal muscle , 2000, The Journal of physiology.

[19]  D. Hardie,et al.  Analysis of the role of the AMP-activated protein kinase in the response to cellular stress. , 2000, Methods in molecular biology.

[20]  B. Saltin,et al.  Maximal perfusion of skeletal muscle in man. , 1985, The Journal of physiology.

[21]  O. H. Lowry CHAPTER 8 – ENZYMATIC CYCLING , 1972 .