Ryanodine receptor fragmentation and sarcoplasmic reticulum Ca²⁺ leak after one session of high-intensity interval exercise

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 112; no. 50; pp. 15492 - 15497
• Main Authors: Place, Nicolas, Ivarsson, Niklas, Venckunas, Tomas, Neyroud, Daria, Brazaitis, Marius, Cheng, Arthur J., Ochala, Julien, Kamandulis, Sigitas, Girard, Sebastien, Volungevičius, Gintautas, Paužas, Henrikas, Mekideche, Abdelhafid, Kayser, Bengt, Martinez-Redondo, Vicente, Ruas, Jorge L., Bruton, Joseph, Truffert, Andre, Lanner, Johanna T., Skurvydas, Albertas, Westerblad, Håkan
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 15.12.2015; National Acad Sciences
• Series: From the Cover
• Subjects: Adult; Animals; Athletes; Biological Sciences; Calcium - metabolism; Exercise - physiology; Humans; Male; Mice; Mice, Inbred C57BL; Muscle Fibers, Skeletal - physiology; Physical Endurance; Reactive Oxygen Species - metabolism; Recreation; Ryanodine Receptor Calcium Release Channel - metabolism; Sarcoplasmic Reticulum - metabolism; ryanodine receptor 1; skeletal muscle; Ca2; high-intensity exercise; reactive oxygen species
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1507176112

High-intensity interval training (HIIT) is a time-efficient way of improving physical performance in healthy subjects and in patients with common chronic diseases, but less so in elite endurance athletes. The mechanisms underlying the effectiveness of HIIT are uncertain. Here, recreationally active human subjects performed highly demanding HIIT consisting of 30-s bouts of all-out cycling with 4-min rest in between bouts (≤3 min total exercise time). Skeletal muscle biopsies taken 24 h after the HIIT exercise showed an extensive fragmentation of the sarcoplasmic reticulum (SR) Ca²⁺ release channel, the ryanodine receptor type 1 (RyR1). The HIIT exercise also caused a prolonged force depression and triggered major changes in the expression of genes related to endurance exercise. Subsequent experiments on elite endurance athletes performing the same HIIT exercise showed no RyR1 fragmentation or prolonged changes in the expression of endurance-related genes. Finally, mechanistic experiments performed on isolated mouse muscles exposed to HIIT-mimicking stimulation showed reactive oxygen/nitrogen species (ROS)-dependent RyR1 fragmentation, calpain activation, increased SR Ca²⁺ leak at rest, and depressed force production due to impaired SR Ca²⁺ release upon stimulation. In conclusion, HIIT exercise induces a ROS-dependent RyR1 fragmentation in muscles of recreationally active subjects, and the resulting changes in muscle fiber Ca²⁺-handling trigger muscular adaptations. However, the same HIIT exercise does not cause RyR1 fragmentation in muscles of elite endurance athletes, which may explain why HIIT is less effective in this group.