Artículos de revistas
IMMUNOMETABOLIC RESPONSES TO CONCURRENT TRAINING: THE EFFECTS OF EXERCISE ORDER IN RECREATIONAL WEIGHTLIFTERS
Fecha
2016-07-01Registro en:
Journal Of Strength And Conditioning Research. Philadelphia: Lippincott Williams & Wilkins, v. 30, n. 7, p. 1960-1967, 2016.
1064-8011
10.1519/JSC.0000000000001281
WOS:000378605900022
Autor
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Coastal Carolina Univ
Institución
Resumen
The relationship between immunometabolic response and performance is not well understood. This study evaluated the influence of concurrent strength and high-intensity aerobic sequence of exercise order between sessions on strength performance, metabolic, and inflammatory response. Eleven recreational weightlifters underwent the following 2 randomized sessions: (a) strength-aerobic exercise order (SA) and (b) aerobic-strength exercise order (AS). Blood samples were collected before (Pre) and immediately after the first exercise (Post-1) and the second exercise (Post-2) of each session. The SA condition presented a higher number of repetitions (SA: 54 +/- 15 vs. AS: 43 +/- 12) and total volume (SA: 7,265 6 2,323 vs. AS: 5,794 +/- 1846 kg) than the AS condition (both p = 0.001). Glucose was higher in Pre when compared with post-1 in both orders (p <= 0.05); changes in lactate were time-dependent in the different orders (p <= 0.05); however, AS post-2 lactate was lower when compared with SA post-2 (p <= 0.05). Interleukin-6 levels showed time-dependent changes for both exercise orders (p <= 0.05). Tumor necrosis factor alpha (TNF-alpha) level was increased only in AS post-1 (AS: pre = 21.91 +/- 35.47, post-1 = 26.99 +/- 47.69 pg.ml(-1) vs. SA: pre = 25.74 +/- 43.64, post-1 = 29.74 +/- 46.05 pg.ml(-1), p <= 0.05). These results suggest that concurrent training order exhibits different immunometabolic responses and, at least in part, can be associated with the acute decline in strength performance induced by concurrent exercise. Our results point to a possible role of TNF-alpha (post-1 AS condition) as a trigger to restore the energy demand by providing substrates to help maintain contractile activity in skeletal muscle.