Cargando…
Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment
BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic respo...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406499/ https://www.ncbi.nlm.nih.gov/pubmed/15086961 http://dx.doi.org/10.1186/1471-2210-4-4 |
_version_ | 1782121389086474240 |
---|---|
author | Corteling, Randolph Trifilieff, Alexandre |
author_facet | Corteling, Randolph Trifilieff, Alexandre |
author_sort | Corteling, Randolph |
collection | PubMed |
description | BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic response, airway inflammation and hyperreactivity and their responses to budesonide. RESULTS: Following an acute ovalbumin challenge, actively sensitised BALB/c mice developed a time-dependent increase in interleukin-4 and interleukin-5 production and inflammatory cell influx into bronchoalveolar lavage fluid. Apart from an increased number of lymphocytes in female mice at day 3 post-challenge, none of the above parameters were affected by gender. Blood leukocyte numbers were also unaffected, whereas a two-fold increase in total serum immunoglobulin E was observed in female mice. Budesonide, given intranasally, did not affect the blood parameters, but dose-dependently inhibited the pulmonary inflammation and airway hyperreactivity in both male and female mice. Female mice were slightly less sensitive to budesonide's inhibitory action on interleukin-5 production and the development of airway hyperreactivity. CONCLUSIONS: Our results suggest that, apart from a 2-fold increase in serum immunoglobulin E levels observed in female mice, gender is not a major factor in the present murine model of ovalbumin-induced lung inflammation. In contrast, gender might slightly influence the potency of test compounds such as steroids. |
format | Text |
id | pubmed-406499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4064992004-05-13 Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment Corteling, Randolph Trifilieff, Alexandre BMC Pharmacol Research Article BACKGROUND: Evidence suggests that gender differences exist in the severity of many immunological diseases and their response to glucocorticosteroid treatment. In this report, we have used a murine model of ovalbumin-induced lung inflammation to address whether gender could affect the systemic response, airway inflammation and hyperreactivity and their responses to budesonide. RESULTS: Following an acute ovalbumin challenge, actively sensitised BALB/c mice developed a time-dependent increase in interleukin-4 and interleukin-5 production and inflammatory cell influx into bronchoalveolar lavage fluid. Apart from an increased number of lymphocytes in female mice at day 3 post-challenge, none of the above parameters were affected by gender. Blood leukocyte numbers were also unaffected, whereas a two-fold increase in total serum immunoglobulin E was observed in female mice. Budesonide, given intranasally, did not affect the blood parameters, but dose-dependently inhibited the pulmonary inflammation and airway hyperreactivity in both male and female mice. Female mice were slightly less sensitive to budesonide's inhibitory action on interleukin-5 production and the development of airway hyperreactivity. CONCLUSIONS: Our results suggest that, apart from a 2-fold increase in serum immunoglobulin E levels observed in female mice, gender is not a major factor in the present murine model of ovalbumin-induced lung inflammation. In contrast, gender might slightly influence the potency of test compounds such as steroids. BioMed Central 2004-04-15 /pmc/articles/PMC406499/ /pubmed/15086961 http://dx.doi.org/10.1186/1471-2210-4-4 Text en Copyright © 2004 Corteling and Trifilieff; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Corteling, Randolph Trifilieff, Alexandre Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title | Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title_full | Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title_fullStr | Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title_full_unstemmed | Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title_short | Gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
title_sort | gender comparison in a murine model of allergen-driven airway inflammation and the response to budesonide treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC406499/ https://www.ncbi.nlm.nih.gov/pubmed/15086961 http://dx.doi.org/10.1186/1471-2210-4-4 |
work_keys_str_mv | AT cortelingrandolph gendercomparisoninamurinemodelofallergendrivenairwayinflammationandtheresponsetobudesonidetreatment AT trifilieffalexandre gendercomparisoninamurinemodelofallergendrivenairwayinflammationandtheresponsetobudesonidetreatment |