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

被引:14
|
作者
Ahmad, Tanveer [1 ]
Mabalirajan, Ulaganathan [1 ]
Joseph, Duraisamy Arul [1 ]
Makhija, Lokesh [1 ]
Singh, Vijay Pal [1 ]
Ghosh, Balaram [1 ]
Agrawal, Anurag [1 ]
机构
[1] Inst Genom & Integrat Biol, Ctr Excellence Translat Res Asthma & Lung Dis TRi, Delhi 110007, India
关键词
inflammometry; asthma; ASTHMA; DISEASE; PLETHYSMOGRAPHY; RESPONSIVENESS; CHILDREN; MOUSE; NO;
D O I
10.1152/japplphysiol.00235.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Ahmad T, Mabalirajan U, Joseph DA, Makhija L, Singh VP, Ghosh B, Agrawal A. Exhaled nitric oxide estimation by a simple and efficient noninvasive technique and its utility as a marker of airway inflammation in mice. J Appl Physiol 107: 295-301, 2009. First published April 30, 2009; doi:10.1152/japplphysiol.00235.2009.-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.
引用
收藏
页码:295 / 301
页数:7
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