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1 School of Sport and Exercise Sciences, University of Birmingham, Birmingham, West Midlands, United Kingdom
2 Department of Immunology, University of Birmingham, Birmingham, West Midlands, United Kingdom
3 Consumer Healthcare, GlaxoSmithKline, United Kingdom
4 School of Sport and Exercise Sciences, Loughborough University, Loughborough, West Midlands, United Kingdom
* To whom correspondence should be addressed. E-mail: m.gleeson{at}lboro.ac.uk.
The present study was undertaken to examine the role of the exercise-induced stress hormone response on the regulation of type 1 and type 2 T lymphocyte intracellular cytokine production. Subjects performed 2.5 hr of cycling exercise at 65% maximal O2 uptake while ingesting a 6.4% carbohydrate (CHO) solution, 12.8% CHO solution or a placebo. Peripheral whole blood samples were stimulated and stained for T lymphocyte surface antigens (CD4 and CD8). Cells were then permeabilised, stained for intracellular cytokines and analysed using flow cytometry. Exercise resulted in a decrease (P<0.05) in the number and percentage of IFN-
positive CD4+ and CD8+ T lymphocytes. These stimulated cells produced less IFN-
immediately post-exercise (P<0.05) and 2-hr post-exercise (P<0.05) compared with pre-exercise. However, CHO ingestion, which attenuated the exercise-induced stress hormone response compared with placebo (P<0.05), prevented both the decrease in the number and percentage of IFN-
positive CD4+ and CD8+ T lymphocytes, and the suppression of IFN-
production from stimulated CD4+ and CD8+ T lymphocytes. There was no effect of exercise on the number of, or cytokine production from, IL-4 positive CD4+ or CD8+ T lymphocytes. These data provide support for the role of exercise-induced elevations in stress hormones in the regulation of type 1 T lymphocyte cytokine production and distribution.
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