Background
One feature of allergic asthma, the early allergic reaction (EAR), is not present in the commonly used mouse models. We therefore investigated the mediators involved in EAR in a guinea pig in vivo model of allergic airway inflammation.
Method
Animals were sensitized using a single ovalbumin (OVA)/alum injection and challenged with aerosolized OVA on day 14. On day 15, airway resistance was assessed after challenge with OVA or methacholine using the forced oscillation technique, and lung tissue was prepared for histology.
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Results
The contribution of mast cell mediators was investigated using histamine 1 receptor (pyrilamine) and cysteinyl leukotriene 1 receptor (montelukast) antagonists, and the cyclooxygenase inhibitor indomethacin as single treatment, or as dual or triple combinations. OVA-sensitized and challenged animals demonstrated airway hyperresponsiveness to methacholine, and lung tissue eosinophilic inflammation. Antigen challenge induced a strong EAR in the sensitized animals. Treatment with a single compound, or indomethacin together with pyrilamine or montelukast, did not reduce the antigen-induced airway resistance. In contrast, dual treatment with pyrilamine together with montelukast, or triple inhibitor treatment, attenuated approximately 70% of the EAR.
Conclusion
We conclude that, as in humans, the guinea pig allergic inflammation model exhibit both EAR and airway hyperresponsiveness, supporting its suitability for in vivo investigations of the effects of mast cell activation with relevance to asthma. Moreover, the known mast cell mediators histamine and leukotriene caused the main part of the EAR. The data lend further support to the concept that combination therapy with selective inhibitors of key mediators could improve asthma management.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.