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ENVIRONMENTAL, EXERCISE AND RESPIRATORY PHYSIOLOGY
1Department of Biomedical Engineering, 2Department of Chemical Engineering and Materials Science, 3Department of Pediatrics, 4General Clinical Research Center, 5Center for Statistical Consulting, and 6Department of Medicine, Division of Pulmonary and Critical Care, University of California, Irvine, California
Submitted 14 March 2006 ; accepted in final form 6 July 2006
Exhaled nitric oxide (NO) is altered in asthmatic subjects with exercise-induced bronchoconstriction (EIB). However, the physiological interpretation of exhaled NO is limited because of its dependence on exhalation flow and the inability to distinguish completely proximal (large airway) from peripheral (small airway and alveolar) contributions. We estimated flow-independent NO exchange parameters that partition exhaled NO into proximal and peripheral contributions at baseline, postexercise challenge, and postbronchodilator administration in steroid-naive mild-intermittent asthmatic subjects with EIB (2443 yr old, n = 9) and healthy controls (2031 yr old, n = 9). The mean ± SD maximum airway wall flux and airway diffusing capacity were elevated and forced expiratory flow, midexpiratory phase (FEF2575), forced expiratory volume in 1 s (FEV1), and FEV1/forced vital capacity (FVC) were reduced at baseline in subjects with EIB compared with healthy controls, whereas the steady-state alveolar concentration of NO and FVC were not different. Compared with the response of healthy controls, exercise challenge significantly reduced FEV1 (23 ± 15%), FEF2575 (37 ± 18%), FVC (12 ± 12%), FEV1/FVC (13 ± 8%), and maximum airway wall flux (35 ± 11%) relative to baseline in subjects with EIB, whereas bronchodilator administration only increased FEV1 (+20 ± 21%), FEF2575 (+56 ± 41%), and FEV1/FVC (+13 ± 9%). We conclude that mild-intermittent steroid-naive asthmatic subjects with EIB have altered airway NO exchange dynamics at baseline and after exercise challenge but that these changes occur by distinct mechanisms and are not correlated with alterations in spirometry.
asthma; model; inflammation
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