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Increased antioxidant activity after exposure of ozone in murine asthma model

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...

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Autores principales: Kim, Yang Ki, Koo, So My, Kim, Kiup, Uh, Soo-Taek, Jang, Ahnsoo, Park, Choon-Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537081/
https://www.ncbi.nlm.nih.gov/pubmed/28765821
http://dx.doi.org/10.5415/apallergy.2017.7.3.163
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author Kim, Yang Ki
Koo, So My
Kim, Kiup
Uh, Soo-Taek
Jang, Ahnsoo
Park, Choon-Sik
author_facet Kim, Yang Ki
Koo, So My
Kim, Kiup
Uh, Soo-Taek
Jang, Ahnsoo
Park, Choon-Sik
author_sort Kim, Yang Ki
collection PubMed
description 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.
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spelling pubmed-55370812017-08-01 Increased antioxidant activity after exposure of ozone in murine asthma model Kim, Yang Ki Koo, So My Kim, Kiup Uh, Soo-Taek Jang, Ahnsoo Park, Choon-Sik Asia Pac Allergy Original Article 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. Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2017-07 2017-07-26 /pmc/articles/PMC5537081/ /pubmed/28765821 http://dx.doi.org/10.5415/apallergy.2017.7.3.163 Text en Copyright © 2017. Asia Pacific Association of Allergy, Asthma and Clinical Immunology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Yang Ki
Koo, So My
Kim, Kiup
Uh, Soo-Taek
Jang, Ahnsoo
Park, Choon-Sik
Increased antioxidant activity after exposure of ozone in murine asthma model
title Increased antioxidant activity after exposure of ozone in murine asthma model
title_full Increased antioxidant activity after exposure of ozone in murine asthma model
title_fullStr Increased antioxidant activity after exposure of ozone in murine asthma model
title_full_unstemmed Increased antioxidant activity after exposure of ozone in murine asthma model
title_short Increased antioxidant activity after exposure of ozone in murine asthma model
title_sort increased antioxidant activity after exposure of ozone in murine asthma model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537081/
https://www.ncbi.nlm.nih.gov/pubmed/28765821
http://dx.doi.org/10.5415/apallergy.2017.7.3.163
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