Cytokine response to acute running in recreationally-active and endurance-trained men

European journal of applied physiology(2013)

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Abstract
To compare the cytokine response to exhaustive running in recreationally-active (RA) and endurance-trained (ET) men. Eleven RA men (VO 2max 55 ± 7 mL·min −1 ·kg −1 ) and 10 ET men (VO 2max 68 ± 7 mL·min −1 ·kg −1 ) followed a controlled diet and refrained from volitional exercise for 8 days. On the fourth day, participants completed 60 min of treadmill running (65 % VO 2max ), followed by intermittent running to exhaustion (70 % VO 2max ). Fasting blood was obtained at baseline, after 20, 40 and 60 min of exercise, at the end of intermittent exercise, during 2 h of recovery and on four follow-up days (FU1–FU4). Tumour necrosis factor-alpha (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-1 receptor antagonist (IL-1ra) and creatine kinase (CK) were measured. Exercise increased the concentrations of all cytokines and CK, but there were no significant differences between groups. IL-1β increased (2.2–2.5-fold, P < 0.001) during exercise, while TNF-α was increased (1.6–2.0-fold, P < 0.001) during exercise and for 2 h post-exercise. IL-6 (71–84-fold, P < 0.001) and IL-1ra (52–64-fold, P < 0.001) were increased throughout exercise and up to FU1, peaking immediately after exercise and at 1.5–2 h post-exercise, respectively. CK concentrations were increased ( P < 0.001) throughout exercise and up to FU4, peaking at FU1, but were not associated with changes in any cytokines. Exhaustive running resulted in modest and transient increases in TNF-α and IL-1β, and more marked and prolonged increases in IL-6 and IL-1ra, but improved training status did not affect this response. Increased CK might indicate either exercise-induced muscle cell disruption or increased cell permeability, although neither appears to have contributed to the increased cytokine concentrations.
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Key words
Acute exercise, Training status, Tumour necrosis factor-α, Interleukin-1β, Interleukin-6, Interleukin-1 receptor antagonist
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