Abstract
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 (24-43 yr old, n = 9) and healthy controls (20-31 yr old, n = 9). The mean +/- SD maximum airway wall flux and airway diffusing capacity were elevated and forced expiratory flow, midexpiratory phase (FEF(25-75)), forced expiratory volume in 1 s (FEV(1)), and FEV(1)/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 FEV(1) (-23 +/- 15%), FEF(25-75) (-37 +/- 18%), FVC (-12 +/- 12%), FEV(1)/FVC (-13 +/- 8%), and maximum airway wall flux (-35 +/- 11%) relative to baseline in subjects with EIB, whereas bronchodilator administration only increased FEV(1) (+20 +/- 21%), FEF(25-75) (+56 +/- 41%), and FEV(1)/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.
Highlights
NITRIC OXIDE (NO) appears in the exhaled breath and performs many functions in the lungs such as smooth muscle relaxation, host defense, inhibition of platelet aggregation, and neurotransmission
None of the observed changes in JЈawNO and C*ENO postexercise and postbronchodilator administration had any significant correlation with changes in spirometric indexes (FVC, forced expiratory volume in 1 s (FEV1), FEF25–75, and FEV1/forced vital capacity (FVC)) postexercise and postbronchodilator administration for healthy control or exercise-induced bronchoconstriction (EIB) subjects. This is the first study to examine the dynamic relationship in EIB between spirometric indexes and proximal and peripheral nitric oxide (NO) exchange
We found that elevated baseline exhaled NO concentration in subjects with EIB was due primarily to an increase in the airway diffusing capacity of NO, resulting in a larger maximum flux (JЈawNO ϭ DawNO ϫ CawNO) of NO from the airway wall
Summary
NITRIC OXIDE (NO) appears in the exhaled breath and performs many functions in the lungs such as smooth muscle relaxation, host defense, inhibition of platelet aggregation, and neurotransmission. There is a growing body of evidence that suggests CENO has both a proximal (i.e., large airway) and peripheral (i.e., small airway and alveolar) contribution [18, 28, 35, 44, 52]. This contrasts sharply with other endogenously produced gases, such as carbon dioxide, which are excreted mainly in the alveolar region of the lungs. The flow-independent NO exchange parameters can partition CENO into proximal (JЈawNO, DawNO, and CawNO) and peripheral (CANO) contributions and potentially provide insight into the mechanisms of NO exchange in EIB.
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