Exhaled nitric oxide estimation by a simple and efficient noninvasive technique and its utility as a marker of airway inflammation in mice

Centre of Excellence for Translational Research in Asthma and Lung disease (TRiAL), Institute of Genomics and Integrative Biology, Delhi, India Submitted 2 March 2009 ; accepted in final form 29 April 2009 Allergic airway inflammation (AI) is commonly associated with enhanced exhaled nitric oxide (E...

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Veröffentlicht in:Journal of applied physiology (1985) 2009-07, Vol.107 (1), p.295-301
Hauptverfasser: Ahmad, Tanveer, Mabalirajan, Ulaganathan, Joseph, Duraisamy Arul, Makhija, Lokesh, Singh, Vijay Pal, Ghosh, Balaram, Agrawal, Anurag
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Sprache:eng
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Zusammenfassung:Centre of Excellence for Translational Research in Asthma and Lung disease (TRiAL), Institute of Genomics and Integrative Biology, Delhi, India Submitted 2 March 2009 ; accepted in final form 29 April 2009 Allergic airway inflammation (AI) is commonly associated with enhanced exhaled nitric oxide (ENO) in both humans and mice. Since mouse models are being used to understand various mechanisms of asthma, a noninvasive, simple, and reproducible method to determine ENO in mice is required for serial nonterminal assessment that can be used independent of environmental situations in which the ambient air contains substantial amounts of NO as a contaminant. The aim of this study was to noninvasively measure ENO in individual mice and to test its utility as a marker of AI in different models of allergic AI. We modified the existing ENO measuring methods by incorporating flushing and washout steps that allowed simple but reliable measurements under highly variable ambient NO conditions (1–100 ppb). This method was used to serially follow ENO in acute and chronic models of allergic AI in mice. ENO was reproducibly measured by this modified method and was positively correlated to AI in both acute and chronic models of asthma but was not independently related to airway remodeling. Resolution of AI and other related parameters in dexamethasone-treated mice resulted in reduction of ENO, further confirming this association. Restriction of allergen challenge to pulmonary but not nasal airways was associated with a smaller increase in ENO compared with allergen challenge to both. Hence, ENO can now be reliably measured in mice independent of ambient NO levels and is a valid biomarker for AI. However, nasal and pulmonary airways are likely to be independent sources of ENO, and any results must be interpreted as such. inflammometry; asthma Address for reprint requests and other correspondence: A. Agrawal, Inst. of Genomics and Integrative Biology, Mall Road, Delhi-110007, India (e-mail: a.agrawal{at}igib.res.in )
ISSN:8750-7587
1522-1601
DOI:10.1152/japplphysiol.00235.2009