Effects of dexamethasone on the expression of transforming growth factor-beta in the mouse model of allergic rhinitis

Laryngoscope. 2007 Aug;117(8):1323-8. doi: 10.1097/MLG.0b013e318064e84d.

Abstract

Objectives/hypothesis: This study aimed to evaluate the effect of dexamethasone on the expression of transforming growth factor (TGF)-beta in the mouse model of allergic rhinitis.

Study design: Female BALB/c mice were randomly assigned to four groups, including two control groups and two treatment groups.

Methods: General sensitization and local challenge were performed with ovalbumin (OVA). In the treatment groups, dexamethasone was injected intraperitoneally 3 hours before general sensitization or local challenge. Symptom score, eosinophil infiltration, and immunostaining for TGF-beta1 and CD4 in nasal mucosa, and TGF-beta1 and OVA-specific immunoglobulin E (IgE) in sera were analyzed.

Results: Dexamethasone administration before general sensitization reduced the symptom score, OVA-specific IgE, and eosinophil infiltration and increased the serum level of TGF-beta1 significantly. Dexamethasone administration before local challenge reduced only the eosinophil infiltration significantly. Immunoreactivity of TGF-beta1 and CD4 was lower in both treatment groups.

Conclusion: These results suggest that dexamethasone may play an important role in the regulation of allergic reactions by at least two mechanisms; one by suppressing allergic sensitization through decrease of CD4+ T cells and increase of TGF-beta, and the other by suppressing late allergic reactions through the inhibition of proliferation and chemotaxis of inflammatory cells such as eosinophils.

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / pathology
  • Dexamethasone / therapeutic use*
  • Disease Models, Animal
  • Eosinophils / pathology
  • Female
  • Gene Expression / drug effects*
  • Glucocorticoids / therapeutic use*
  • Immunoglobulin E / metabolism
  • Immunohistochemistry
  • Leukocyte Count
  • Mice
  • Mice, Inbred BALB C
  • Nasal Mucosa / immunology
  • Nasal Mucosa / metabolism
  • Nasal Mucosa / pathology
  • Ovalbumin / toxicity
  • RNA, Messenger / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rhinitis, Allergic, Seasonal* / chemically induced
  • Rhinitis, Allergic, Seasonal* / drug therapy
  • Rhinitis, Allergic, Seasonal* / metabolism
  • Transforming Growth Factor beta / genetics*
  • Transforming Growth Factor beta / metabolism

Substances

  • Glucocorticoids
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Immunoglobulin E
  • Dexamethasone
  • Ovalbumin