Proposed short-term model of acute allergic response, without adjuvant use, in the lungs of mice

J Bras Pneumol. 2012 Sep-Oct;38(5):595-604. doi: 10.1590/s1806-37132012000500009.
[Article in English, Portuguese]

Abstract

Objective: To determine whether a short-term protocol using subcutaneous sensitization with ovalbumin, without the use of adjuvants, would induce an eosinophilic response in the lungs of mice similar to that observed in previous, well-established protocols.

Methods: Adult female BALB/c mice were randomized and divided into groups according to the number of sensitizations with ovalbumin and the number/dosage of intranasal ovalbumin challenges. The short-term protocol (10 days) consisted of one sensitization with ovalbumin and three ovalbumin challenges (100 µg). Total and differential cell counts in BAL fluid, levels of eosinophil peroxidase in lung tissue, and histopathological examination of the lungs were performed 24 h after the last ovalbumin challenge.

Results: No significant differences were found among the groups regarding the variables studied. The short-term protocol, as well as the other protocols studied, induced an eosinophilic response similar to that obtained in the positive control.

Conclusions: Subcutaneous sensitization with ovalbumin and without the use of adjuvants resulted in a significant allergic response in the lungs of mice, even in the short-term protocol group. Our findings suggest that this short-term protocol can be used as a first-line pre-clinical test for the study of new medications, reducing the costs and observation periods.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Asthma / enzymology
  • Asthma / pathology*
  • Bronchial Hyperreactivity / enzymology
  • Bronchial Hyperreactivity / pathology*
  • Bronchial Provocation Tests
  • Bronchoalveolar Lavage Fluid / cytology
  • Disease Models, Animal
  • Eosinophil Peroxidase / metabolism*
  • Female
  • Lung / enzymology
  • Lung / pathology*
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin*
  • Pulmonary Eosinophilia / immunology*
  • Pulmonary Eosinophilia / pathology
  • Random Allocation

Substances

  • Ovalbumin
  • Eosinophil Peroxidase