4.6 Article

The effect of exercise-intensity on skeletal muscle stress kinase and insulin protein signaling

Journal

PLOS ONE
Volume 12, Issue 2, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0171613

Keywords

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Funding

  1. Future Leader Fellowship from the National Heart Foundation of Australia [100040]
  2. Australian Governments Collaborative Research Network

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Background Stress and mitogen activated protein kinase (SAPK) signaling play an important role in glucose homeostasis and the physiological adaptation to exercise. However, the effects of acute high-intensity interval exercise (HIIE) and sprint interval exercise (SIE) on activation of these signaling pathways are unclear. Methods Eight young and recreationally active adults performed a single cycling session of HIIE (5 x 4 minutes at 75% W-max), SIE (4 x 30 second Wingate sprints), and continuous moderate- intensity exercise work-matched to HIIE (CMIE; 30 minutes at 50% of W-max), separated by a minimum of 1 week. Skeletal muscle SAPK and insulin protein signaling were measured immediately, and 3 hours after exercise. Results SIE elicited greater skeletal muscle NF-kappa B p65 phosphorylation immediately after exercise (SIE: similar to 40%; HIIE: similar to 4%; CMIE; similar to 13%; p < 0.05) compared to HIIE and CMIE. AS160(Ser588) phosphorylation decreased immediately after HIIE (similar to-27%; p < 0.05), and decreased to the greatest extent immediately after SIE (similar to-60%; p < 0.05). Skeletal muscle JNK (similar to 42%; p < 0.05) and p38 MAPK (similar to 171%; p < 0.05) phosphorylation increased, and skeletal muscle Akt(Ser473) phosphorylation (similar to-32%; p < 0.05) decreased, to a similar extent immediately after all exercise protocols. AS160(Ser588) phosphorylation was similar to baseline three hours after SIE (similar to-12%; p > 0.05), remained lower 3 hours after HIIE (similar to-34%; p < 0.05), and decreased 3 hours after CMIE (similar to-33%; p < 0.05). Conclusion Despite consisting of less total work than CMIE and HIIE, SIE proved to be an effective stimulus for the activation of stress protein kinase signaling pathways linked to exercise-mediated adaptation of skeletal muscle. Furthermore, post-exercise AS160(Ser588) phosphorylation decreased in an exercise-intensity and post-exercise time-course dependent manner.

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