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Cold weather exercise and airway cytokine expression.
|Title||Cold weather exercise and airway cytokine expression.|
|Publication Type||Journal Article|
|Year of Publication||2005|
|Authors||Davis MS, Malayer JR, Vandeventer L, Royer CM, McKenzie EC, Williamson KK|
|Journal||Journal of applied physiology (Bethesda, Md. : 1985)|
|Date Published||2005 Jun|
|Keywords||Animals, Bronchoalveolar Lavage Fluid, Cold Temperature, Cross-Over Studies, Cytokines, Erythroblasts, Gene Expression Regulation, Horses, Physical Conditioning, Animal, Weather|
Athletes who perform repeated exercise while breathing cold air have a high prevalence of asthmalike chronic airway disease, but the mechanism linking such activity to airway inflammation is unknown. We used a novel animal model (exercising horses) to test the hypothesis that exercise-induced chronic airway disease is caused by exposure of intrapulmonary airways to unconditioned air, resulting in the upregulation of cytokine expression. Bronchoalveolar lavage fluid (BALF) was obtained from eight horses 5 h after submaximal exercise while they breathed room temperature or subfreezing air in a random crossover design. BALF total and differential nucleated cell counts were determined, and relative cytokine mRNA expression in BALF nucleated cells was quantified by real-time RT-PCR using primer and probe sequences specific for equine targets. There were no significant changes in total or differential cell concentrations between BALF recovered after warm and cold air exercise, although there was a strong trend toward increased concentrations of airway epithelial cells after cold air exercise (P = 0.0625). T(H)2 cytokines IL-4, IL-5, and IL-10 were preferentially upregulated after cold air exercise 12-, 9-, and 10-fold, respectively, compared with warm air exercise. Other cytokines (IL-2 and IL-6) were upregulated to a lesser extent (6- and 3-fold, respectively) or not at all (IL-1, IL-8, IFN-gamma, and TNF-alpha). These results suggest that cold weather exercise can lead to asthmalike airway disease through the local induction of cytokines typical of the T(H)2 phenotype.
|Alternate Journal||J. Appl. Physiol.|