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Salivary Lymphocyte Responses Following Acute Anaerobic Exercise in a Cool Environment

  • Autores: Lara A. Carlson, Michael A. Lawrence, LeCavalier Kaylee, Alexander J. Koch
  • Localización: Journal of strength and conditioning research: the research journal of the NSCA, ISSN 1064-8011, Vol. 31, Nº. 5, 2017, págs. 1236-1240
  • Idioma: inglés
  • Texto completo no disponible (Saber más ...)
  • Resumen
    • The purpose of this study was to examine the impact of anaerobic training on salivary lymphocytes (s-LYMPH), and further determine whether these responses differ between cool vs. thermoneutral environments. Nine lightly clothed (~0.3 clo) volunteers (7/2 women/men: age, 21 ± 1 years; height, 168.7 ± 7.3 cm; weight, 66.4 ± 8.4 kg; body fat, 20.6 ± 7.6%) completed speed, agility, and quickness (SAQ) sessions in both warm (18.9° C; Biddeford) and cool (10.4° C; Thorsmörk) temperatures. The SAQ sessions consisted of 3 trials of 20-m sprints, 40-m sprints, t-tests, and box drills, and two 300-yd shuttle runs in both conditions. Saliva samples via passive drool were collected at baseline, immediately postexercise, and after 2 hours of recovery. The s-LYMPH increased (p < 0.001) immediately postexercise, followed by a decrease (p < 0.001) below baseline values after 2 hours of recovery in both environments. The s-LYMPH counts were lower (p < 0.001) for the cool environment than for the thermoneutral environment. The s-LYMPH counts increased postexercise, followed by a decrease after 2 hours of recovery regardless of environment. Acute anaerobic exercise induced transient changes in s-LYMPH counts similar to that observed in peripheral blood. Compared with baseline measures, changes in s-LYMPH were of a smaller magnitude after exercise in the cool environment compared with thermoneutral environment. In summary, there is no indication that exercise in the cool environment presented a greater challenge to the subjects' immunity. Rather, these data indicate exercise in a cool environment produces smaller fluctuations in salivary immune cells compared with resting levels.


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