Open Access
Acute molecular responses to concurrent resistance and high‐intensity interval exercise in untrained skeletal muscle
Author(s) -
Pugh Jamie K.,
Faulkner Steve H.,
Jackson Andrew P.,
King James A.,
Nimmo Myra A.
Publication year - 2015
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.12364
Subject(s) - myostatin , high intensity interval training , interval training , medicine , skeletal muscle , endurance training , endocrinology , leg press , insulin resistance , resistance training , cardiology , insulin
Abstract Concurrent training involving resistance and endurance exercise may augment the benefits of single‐mode training for the purpose of improving health. However, muscle adaptations, associated with resistance exercise, may be blunted by a subsequent bout of endurance exercise, via molecular interference. High‐intensity interval training ( HIIT ), generating similar adaptations to endurance exercise, may offer an alternative exercise mode to traditional endurance exercise. This study examined the influence of an acute HIIT session on the molecular responses following resistance exercise in untrained skeletal muscle. Ten male participants performed resistance exercise (4 × 8 leg extensions, 70% 1 RM , ( RE )) or RE followed by HIIT (10 × 1 min at 90% HR max , ( RE + HIIT )). Muscle biopsies were collected from the vastus lateralis before, 2 and 6 h post‐ RE to determine intramuscular protein phosphorylation and mRNA responses. Phosphorylation of Akt (Ser 473 ) decreased at 6 h in both trials ( P < 0.05). Phosphorylation of mTOR (Ser 2448 ) was higher in RE + HIIT ( P < 0.05). All PGC ‐1 α mRNA variants increased at 2 h in RE + HIIT with PGC ‐1 α and PGC ‐1 α ‐ex1b remaining elevated at 6 h, whereas RE ‐induced increases at 2 and 6 h for PGC ‐1 α ‐ex1b only ( P < 0.05). Myostatin expression decreased at 2 and 6 h in both trials ( P < 0.05). Mu RF ‐1 was elevated in RE + HIIT versus RE at 2 and 6 h ( P < 0.05). Atrogin‐1 was lower at 2 h, with FOXO 3A downregulated at 6 h ( P < 0.05). These data do not support the existence of an acute interference effect on protein signaling and mRNA expression, and suggest that HIIT may be an alternative to endurance exercise when performed after resistance exercise in the same training session to optimize adaptations.