Effects of Quercetin Treatment on Epithelium-derived Cytokines and Epithelial Cell Apoptosis in Allergic Airway Inflammation Mice Model

• Published in: Iranian journal of allergy, asthma, and immunology Vol. 15; no. 6; pp. 487 - 497
• Main Authors: Caglayan Sozmen, Sule, Karaman, Meral, Cilaker Micili, Serap, Isik, Sakine, Bagriyanik, Alper, Arikan Ayyildiz, Zeynep, Uzuner, Nevin, Anal, Ozden, Karaman, Ozkan
• Format: Journal Article
• Language: English
• Published: Iran Tehran University of Medical Sciences 01.12.2016
• Subjects: Airway management; Allergens; Animals; Antioxidants - pharmacology; Apoptosis; Apoptosis - drug effects; Asthma; Asthma - immunology; Bronchus; Caspase 3 - drug effects; Caspase 3 - immunology; Caspase-3; Cysteine; Cytokines; Cytokines - drug effects; Cytokines - immunology; Dexamethasone; Disease Models, Animal; DNA nucleotidylexotransferase; Enzyme-linked immunosorbent assay; Epithelial cells; Epithelium; Experiments; Flavonoids; Goblet cells; Goblet Cells - cytology; Goblet Cells - drug effects; Immunization; Immunoglobulin E; In Situ Nick-End Labeling; Inflammation; Inhalation; Interleukin 4; Interleukin-33 - drug effects; Interleukin-33 - immunology; Interleukin-4 - immunology; Interleukins - immunology; Lavage; Lung - cytology; Lung - drug effects; Lung - immunology; Lung - pathology; Mast Cells - cytology; Mast Cells - drug effects; Mice; Mice, Inbred BALB C; Mucous membrane; Ovalbumin; Quercetin; Quercetin - pharmacology; Random Allocation; Respiratory Hypersensitivity - immunology; Respiratory Mucosa - drug effects; Respiratory Mucosa - immunology; Respiratory Mucosa - pathology; Respiratory tract; Respiratory tract diseases; Smooth muscle; Studies; Thymic stromal lymphopoietin; Thymus; Allergic airway inflammation; Mouse model; Antiinflammatory effects; Quercetin
• ISSN: 1735-1502; 1735-5249

Quercetin is a dietary flavonoid which has anti-inflammatory effects. This study aimed to evaluate the influence of quercetin on histopathological aspects and airway epithelium in  allergic airway  inflammation mice model. Twenty-eight BALB/c mice were randomly divided into four groups: Group I (control), Group II (untreated mice with allergic airway inflammation), Group III (allergic airway inflammation quercetin-treated [16mg/kg/day]), Group IV (allergic airway inflammation dexamethasone-treated [1mg/kg/day]). Ovalbumin was administered intraperitoneally and via inhalation to achieve allergic airway inflammation mice model and treatments were also given intraperitoneally. Epithelium thickness, subepithelial smooth muscle thickness, number of mast and goblet cells, and basement membrane thickness were examined on samples isolated from lung. Immunohistochemical evaluationof lung tissues was performed using  IL-25, IL-33, thymic stromal lymphopoietin (TSLP), terminal deoxynucleotidyl transferase-mediated dUTP nick endlabeling (TUNEL) and cysteine-dependent aspartate-specific proteases(caspase)-3 antibodies. IL-4, IL-25, IL-33, TSLP were quantified in bronchoalveolar lavage (BAL) and OVAspecific IgE levels was measured in serum by standard ELISA protocols. IL-25, IL-33, thymic stromal lymphopoietin (TSLP) and cysteine-dependent aspartate-specific proteases (caspase)-3. Quercetin treatment led to lower epithelial thickness, subepithelial smooth muscle thickness, goblet and mast cell numbers compared to untreated  mice with allergic airway inflammation (p<0.05). However, quercetin treatment was not effective on improving basal membane thickness. Immunohistochemical scores of IL-25, IL-33, TSLP, caspase-3 and TUNEL were lower in quercetin-treated mice  t compared to untreated mice with allergic airway inflammation (p<0.05). IL-4, IL-25, IL-33, TSLP levels in BAL and OVA-specific IgE in serum were lower in quercetin treated mice compared to untreated mice (p<0.05). These findings suggest that quercetin improves chronic histopathological changes except basal membrane thickness in lung tissue and its beneficial effects on inflammation might be related to modulating epithelium derived cytokines and epithelial apoptosis.