Increased antioxidant activity after exposure of ozone in murine asthma model
10.5415/apallergy.2017.7.3.163
- Author:
Yang Ki KIM
1
;
So My KOO
;
Kiup KIM
;
Soo Taek UH
;
Ahnsoo JANG
;
Choon Sik PARK
Author Information
1. Division of Respiratory and Allergy Medicine, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea. uhs@schmc.ac.kr
- Publication Type:Original Article
- Keywords:
Asthma;
Oxidants;
Antioxidants;
Mice;
Ozone
- MeSH:
Air Pollutants;
Animals;
Antioxidants;
Asthma;
Blotting, Western;
Bronchoalveolar Lavage;
Eosinophils;
Glutathione;
Humans;
Immunohistochemistry;
Lung;
Methacholine Chloride;
Mice;
Ovalbumin;
Oxidants;
Oxygen;
Ozone;
Proliferating Cell Nuclear Antigen;
Respiratory Hypersensitivity
- From:
Asia Pacific Allergy
2017;7(3):163-170
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Ozone is well known as an important component of ambient air pollutants. Ozone can aggravate respiratory symptoms in patients with bronchial asthma, but, not in healthy person. We hypothesized asthma itself may show different response to ozone compared to nonasthma. OBJECTIVE: This study was performed to evaluate the differences of response to ozone between normal and asthmatic mice model in terms of status of oxidant injury and antioxidant activity. METHODS: Three parts per million of ozone was exposed to ovalbumin (OVA)-induced murine asthma model for 3 hours at 3, 7, 14, 21 days after completion of asthma model. Airway responsiveness to methacholine was measured after completion of asthma model. Bronchoalveolar lavage (BAL), protein extraction from lung for Western blot and immunohistochemistry of 4-hydroxy-2-nonenal (4-HNE), proliferating cell nuclear antigen (PCNA), NF-E2 related factor 2 (Nrf-2), and activity of glutathione were performed at before and each ozone exposure day. RESULTS: Airway hyper-responsiveness and increased eosinophils in BAL fluid were observed in asthma model. In asthma model, the expression of 4-HNE already more increased at baseline (without ozone) compared to those in sham model. This increased expression is more enhanced at 3 days after ozone exposure. The expression of PCNA was significantly increased in OVA-model compared to those in sham model. The expression of Nrf-2 was observed at baseline, and 3 and 7 days after exposure ozone in asthma model, but not in sham model. The activity of glutathione increased significantly after exposure of ozone, but not in sham model. CONCLUSION: Murine asthma model has enhanced oxygen toxicity and antioxidant activity response to ozone.
