Intranasal challenge with increasing ovalbumin doses differently affects airway hyperresponsiveness and inflammatory cell accumulation in mouse model of asthma

Inflamm Res. 2009 Nov;58(11):773-81. doi: 10.1007/s00011-009-0046-2. Epub 2009 May 8.

Abstract

Objective: To investigate whether challenge with increasing allergen doses could differently affect allergen-induced airway hyperresponsiveness (AHR) and inflammatory cell accumulation in mouse model of asthma, providing an experimental model to investigate their relationship.

Material and methods: AHR and accumulation of inflammatory cells in bronchoalveolar lavage fluid (BALF) and into the lungs were compared in ovalbumin-sensitized mice that were challenged intranasally with 2.5, 10, 25 or 100 microg of ovalbumin/mouse.

Results: Both AHR and inflammatory cell accumulation were proportional to the ovalbumin dose used for challenge. However, in group challenged with 10 microg of ovalbumin airway inflammation was present, although allergen-induced AHR was not detected. Additional analysis indicated that neither mucous hyperproduction nor eosinophil degranulation could be correlated to presence of AHR in this model, whereas concentration of interleukin (IL)-13 in BALF was increased only in those groups in which AHR was present.

Conclusions: Altogether, intranasal challenge of mice with increasing allergen doses could serve as a suitable experimental system for investigation of mechanisms by which airway inflammation leads to allergen-induced AHR. Our initial findings are in line with previous reports that dissociate AHR from amount of eosinophil accumulation and imply the role of IL-13 in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal*
  • Animals
  • Asthma / immunology*
  • Bronchial Hyperreactivity* / chemically induced
  • Bronchial Hyperreactivity* / immunology
  • Bronchoalveolar Lavage Fluid / cytology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cytokines / immunology
  • Disease Models, Animal
  • Eosinophil Peroxidase / metabolism
  • Eosinophils / immunology
  • Humans
  • Inflammation / immunology*
  • Interleukin-13 / immunology
  • Lung / cytology
  • Lung / immunology
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin* / administration & dosage
  • Ovalbumin* / immunology

Substances

  • Cytokines
  • Interleukin-13
  • Ovalbumin
  • Eosinophil Peroxidase