Antileukotriene reverts the early effects of inflammatory response of distal parenchyma in experimental chronic allergic inflammation

Biomed Res Int. 2013:2013:523761. doi: 10.1155/2013/523761. Epub 2013 Sep 15.

Abstract

Aims: Compare the effects of montelukast or dexamethasone in distal lung parenchyma and airway walls of guinea pigs (GP) with chronic allergic inflammation.

Methods: GP have inhaled ovalbumin (OVA group-2x/week/4weeks). After the 4th inhalation, GP were treated with montelukast or dexamethasone. After 72 hours of the 7th inhalation, GP were anesthetised, and lungs were removed and submitted to histopathological evaluation.

Results: Montelukast and dexamethasone treatments reduced the number of eosinophils in airway wall and distal lung parenchyma compared to OVA group (P < 0.05). On distal parenchyma, both treatments were effective in reducing RANTES, NF- κ B, and fibronectin positive cells compared to OVA group (P < 0.001). Montelukast was more effective in reducing eotaxin positive cells on distal parenchyma compared to dexamethasone treatment (P < 0.001), while there was a more expressive reduction of IGF-I positive cells in OVA-D group (P < 0.001). On airway walls, montelukast and dexamethasone were effective in reducing IGF-I, RANTES, and fibronectin positive cells compared to OVA group (P < 0.05). Dexamethasone was more effective in reducing the number of eotaxin and NF- κ B positive cells than Montelukast (P < 0.05).

Conclusions: In this animal model, both treatments were effective in modulating allergic inflammation and remodeling distal lung parenchyma and airway wall, contributing to a better control of the inflammatory response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / administration & dosage
  • Administration, Inhalation
  • Animals
  • Chronic Disease / drug therapy
  • Cyclopropanes
  • Dexamethasone / administration & dosage
  • Disease Models, Animal
  • Guinea Pigs
  • Hypersensitivity / drug therapy*
  • Hypersensitivity / pathology
  • Inflammation / chemically induced
  • Inflammation / drug therapy*
  • Inflammation / pathology
  • Leukotriene Antagonists / administration & dosage*
  • Lung / drug effects*
  • Lung / pathology
  • Ovalbumin / toxicity
  • Quinolines / administration & dosage
  • Sulfides

Substances

  • Acetates
  • Cyclopropanes
  • Leukotriene Antagonists
  • Quinolines
  • Sulfides
  • Dexamethasone
  • Ovalbumin
  • montelukast