Glabridin attenuates airway inflammation and hyperresponsiveness in a mice model of ovalbumin-induced asthma

Autor: Saliha Ayşenur Çam, Muhammed Fatih Dogan, Ali Parlar, Seyfullah Oktay Arslan, Fatma Uysal, Elif Merve Tosun
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Male
drug megadose
leukocyte count
aerosol
peak expiratory flow
Pharmacology
Pulmonary function testing
immunoglobulin E
low drug dose
Mice
chemistry.chemical_compound
0302 clinical medicine
methacholine
dose response
ovalbumin-induced airway inflammation
Pharmacology (medical)
Respiratory function
030212 general & internal medicine
Lung
Tidal volume
measurement_unit
Mice
Inbred BALB C

bronchoalveolar lavage fluid
biology
tidal volume
neutrophil
respiratory system
Plethysmography
drug dose comparison
priority journal
body plethysmography
measurement_unit.measuring_instrument
monocyte
Bronchial Hyperreactivity
Bronchoalveolar Lavage Fluid
Glabridin
expiratory reserve volume
medicine.drug
Pulmonary and Respiratory Medicine
Ovalbumin
animal experiment
aluminum hydroxide
dexamethasone
lymphocyte
Article
animal tissue
03 medical and health sciences
Phenols
male
medicine
drug mechanism
Animals
controlled study
eosinophil
immunoglobulin blood level
leukocyte differential count
Peak flow meter
mouse
Asthma
Inflammation
nonhuman
business.industry
animal model
Biochemistry (medical)
glabridin
lung function
asthma
medicine.disease
Isoflavones
respiratory tract diseases
breathing rate
drug efficacy
Disease Models
Animal

peak inspiratory flow
respiratory tract allergy
030228 respiratory system
chemistry
biology.protein
Methacholine
business
protein
Popis: Asthma is an inflammatory disease of the airways of the lungs, which is characterized by airflow obstruction and bronchospasms. Glabridin is a major flavonoid, especially found in root of Glycyrrhiza glabra, and has several pharmacological activities, including antioxidant and anti-inflammatory effects. The anti-asthmatic effect and possible mechanism of glabridin, however, have not been revealed so far. The aim of this study is to investigate the effects and possible mechanisms of glabridin against ovalbumin (OVA)-induced airway hyperresponsiveness (AHR) and inflammation in mice. In male BALB/c mice, asthma was induced by intraperitoneal (i.p) injection of OVA mixed with 2 mg aluminium hydroxide on days 0, 14 and boosted with OVA aerosol challenge on days 21, 22, and 23. Mice were either treated with dexamethasone (i.p, 1 mg/kg) or glabridin (10, 20, and 30 mg/kg) from days 18–23. Pulmonary function parameters such as peak inspiratory flow, peak expiratory flow, tidal volume, expiratory volume, the frequency of breathing, enhanced pause values were evaluated by using whole-body plethysmography. Measurements were performed at baseline and following methacholine (50 mg/mL) challenges. In addition, white blood cells (WBC) count, total protein, and IgE levels were measured in bronchial alveolar lavage fluid (BALF), lung, and serum, respectively. Glabridin (20 or 30 mg/kg) significantly attenuated (p < 0.05) OVA-induced alteration in respiratory parameters. Elevated counts of total WBC, differential WBC (neutrophils, lymphocytes, monocytes, and eosinophils) in BALF and the total protein in lungs and BALF were significantly decreased (p < 0.05) by glabridin (20 or 30 mg/kg). It also significantly attenuated the increased serum IgE levels (p < 0.05). As glabridin reduces the level of serum IgE, the total protein and the count of WBC and improves respiratory function, it may be a novel therapeutic agent in asthma. © 2020 Elsevier Ltd
Databáze: OpenAIRE