Journal
BRAIN BEHAVIOR AND IMMUNITY
Volume 56, Issue -, Pages 246-252Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2016.03.020
Keywords
Running; Cytokines; Inflammation; Oxidative stress; Muscle damage; Soreness
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This study utilized a pro-inflammatory exercise mode to explore potential linkages between increases in 9- and 13-hydroxy-octadecadienoic acid (9 + 13 HODE) and biomarkers for inflammation, oxidative stress, and muscle damage. Male (N = 10) and female (N = 10) runners ran at similar to 70% VO2max for 1.5 h followed by 30 min of downhill running (-10%). Blood samples were taken pre-run and immediately-, 1-h-, and 24-h post-run, and analyzed for 9 + 13 HODE, F-2-isoprostanes, six cytokines, C-reactive protein (CRP), creatine kinase (CK), and myoglobin (MYO). Gender groups performed at comparable relative heart rate and oxygen consumption levels during the 2-h run. All outcome measures increased post-run (time effects, P <= 0.001), with levels near pre-run levels by 24h except for CRP, CK, MYO, and delayed onset of muscle soreness (DOMS). Plasma 9 + 13 HODE increased 314 +/- 38.4% post-run (P < 0.001), 77.3 +/- 15.8% 1-h post-run (P < 0.001), and 40.6 +/- 16.4% 24-h post-exercise (P = 0.024), and F-2-isoprostanes increased 50.8 +/- 8.9% post-run (P < 0.001) and 19.0 +/- 5.3% 1-h post-run (P = 0.006). Post-run increases were comparable between genders for all outcomes except for 9 + 13 HODE (interaction effect, P = 0.024, post-run tending higher in females), IL-10 (P = 0.006, females lower), and DOMS (P = 0.029, females lower). The pre-to-post-run increase in 9 + 13 HODEs was not related to other outcomes except for plasma granulocyte colony stimulating factor (GCSF) (r = -0.710, P < 0.001) and IL-6 (r = -0.457, P = 0.043). Within the context of this study, exercise-induced increases in 9 + 13 HODEs tended higher in females, and were not related to increases in F-2-isoprostanes, muscle damage, or soreness. The negative relationships to GCSF and IL-6 suggest a linkage between 9 + 13 HODES and exercise-induced neutrophil chemotaxis, degranulation, and inflammation. Copyright (C) 2016 Elsevier Inc. All rights reserved.
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