Elevated exhaled nitric oxide in allergen-provoked asthma is associated with airway epithelial iNOS

PLoS One. 2014 Feb 28;9(2):e90018. doi: 10.1371/journal.pone.0090018. eCollection 2014.

Abstract

Background: Fractional exhaled nitric oxide is elevated in allergen-provoked asthma. The cellular and molecular source of the elevated fractional exhaled nitric oxide is, however, uncertain.

Objective: To investigate whether fractional exhaled nitric oxide is associated with increased airway epithelial inducible nitric oxide synthase (iNOS) in allergen-provoked asthma.

Methods: Fractional exhaled nitric oxide was measured in healthy controls (n = 14) and allergic asthmatics (n = 12), before and after bronchial provocation to birch pollen out of season. Bronchoscopy was performed before and 24 hours after allergen provocation. Bronchial biopsies and brush biopsies were processed for nitric oxide synthase activity staining with nicotinamide adenine dinucleotide phosphate diaphorase (NADPH-d), iNOS immunostaining, or gene expression analysis of iNOS by real-time PCR. NADPH-d and iNOS staining were quantified using automated morphometric analysis.

Results: Fractional exhaled nitric oxide and expression of iNOS mRNA were significantly higher in un-provoked asthmatics, compared to healthy controls. Allergic asthmatics exhibited a significant elevation of fractional exhaled nitric oxide after allergen provocation, as well as an accumulation of airway eosinophils. Moreover, nitric oxide synthase activity and expression of iNOS was significantly increased in the bronchial epithelium of asthmatics following allergen provocation. Fractional exhaled nitric oxide correlated with eosinophils and iNOS expression.

Conclusion: Higher fractional exhaled nitric oxide concentration among asthmatics is associated with elevated iNOS mRNA in the bronchial epithelium. Furthermore, our data demonstrates for the first time increased expression and activity of iNOS in the bronchial epithelium after allergen provocation, and thus provide a mechanistic explanation for elevated fractional exhaled nitric oxide in allergen-provoked asthma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allergens*
  • Asthma / enzymology*
  • Asthma / pathology
  • Bronchi / enzymology*
  • Bronchi / pathology
  • Bronchial Provocation Tests
  • Case-Control Studies
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Exhalation
  • Female
  • Gene Expression
  • Humans
  • Male
  • Middle Aged
  • NADPH Dehydrogenase / genetics
  • NADPH Dehydrogenase / metabolism
  • Nitric Oxide / biosynthesis*
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism*
  • Pollen*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Respiratory Mucosa / metabolism
  • Respiratory Mucosa / pathology

Substances

  • Allergens
  • RNA, Messenger
  • Nitric Oxide
  • NOS2 protein, human
  • Nitric Oxide Synthase Type II
  • NADPH Dehydrogenase

Grants and funding

This work was supported by grants from the Swedish Research Council, the Stockholm County Council, the Swedish Cancer- and Allergy Foundation, the Swedish Asthma- and Allergy Foundation, the Swedish Heart-Lung Foundation, the King Gustaf V 80th Birthday Foundation, Karolinska Institutet, Centre for Allergy Research at Karolinska Instituet, Vinnova (CIDaT), Hesselman‚s, Konsul Th C Bergh‚s, Lars Hierta‚s and Tornspiran‚s Foundations. AstraZeneca R&D provided financial support in the form of travel grants and salaried employment. The funders had no other role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.