Journal of Applied Physiology
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J Appl Physiol (October 6, 2005). doi:10.1152/japplphysiol.00008.2005
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Submitted on January 4, 2005
Accepted on October 1, 2005

Examining axial diffusion of nitric oxide in the lungs using heliox and breathhold

Hye-Won Shin1, Peter Condorelli1, and Steven C. George2*

1 Department of Biomedical Engineering, University of California, Irvine, Irvine, CA, USA
2 Department of Biomedical Engineering, University of California, Irvine, Irvine, CA, USA; Department of Chemical Engineering and Materials Science, University of California, Irvine, Irvine, CA, USA

* To whom correspondence should be addressed. E-mail: scgeorge{at}uci.edu.

Exhaled nitric oxide (NO) is highly dependent on exhalation flow; thus, exchange dynamics of NO have been described by multi-compartment models and a series of flow-independent parameters which describe airway and alveolar exchange. Since the flow-independent NO airway parameters characterize features of the airway tissue (e.g., wall concentration), they should also be independent of the physical properties of the insufflating gas. We measured the total mass of NO exhaled (AI,II) from the airways following five different breathhold times (5 to 30 seconds) in healthy adults (21-38 years, n=9) using air and heliox as the insufflating gas, and then modeled AI,II as a function of breathhold time to determine airway NO exchange parameters. Increasing breathhold time results in an increase in AI,II for both air and heliox, but AI,II is reduced by a mean (SD) of 31 (6) % (p<0.04) in the presence of heliox, independent of breathhold time. However, mean (SD) values (air, heliox) for the airway wall diffusing capacity (3.70 (4.18), 3.56 (3.20) pl.s-1.ppb-1), the airway wall concentration (1439 (487), 1503 (644) ppb), and the maximum airway wall flux (4156 (2502), 4412 (2906) pl/s) using a single path trumpet-shaped airway model which considers axial diffusion were independent of the insufflating gas (p>0.55). We conclude that a single path trumpet model which considers axial diffusion captures the essential features of airway wall NO exchange, and confirm earlier reports that the airway wall concentration in healthy adults exceeds 1 ppm and thus approaches physiologic concentrations capable of modulating smooth muscle tone.




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