Cited by 62Chronic Obstructive Pulmonary Disease (COPD) ResearchAsthma and respiratory diseasesAir Quality and Health Impacts

Effects of N-acetylcysteine in ozone-induced chronic obstructive pulmonary disease model

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Li, Feng, Wiegman, Cornelis, Seiffert, Joanna M., Zhu, Jie, Clarke, Colin, Chang, Yan, Bhavsar, Pank, Adcock, Ian +3 more·2013·PLoS ONE

Abstract

INTRODUCTION: Chronic exposure to high levels of ozone induces emphysema and chronic inflammation in mice. We determined the recovery from ozone-induced injury and whether an antioxidant, N-acetylcysteine (NAC), could prevent or reverse the lung damage. METHODS: Mice were exposed to ozone (2.5 ppm, 3 hours/12 exposures, over 6 weeks) and studied 24 hours (24h) or 6 weeks (6W) later. Nac (100 mg/kg, intraperitoneally) was administered either before each exposure (preventive) or after completion of exposure (therapeutic) for 6 weeks. RESULTS: After ozone exposure, there was an increase in functional residual capacity, total lung volume, and lung compliance, and a reduction in the ratio of forced expiratory volume at 25 and 50 milliseconds to forced vital capacity (FEV25/FVC, FEV50/FVC). Mean linear intercept (Lm) and airway hyperresponsiveness (AHR) to acetylcholine increased, and remained unchanged at 6W after cessation of exposure. Preventive NAC reduced the number of BAL macrophages and airway smooth muscle (ASM) mass. Therapeutic NAC reversed AHR, and reduced ASM mass and apoptotic cells. CONCLUSION: Emphysema and lung function changes were irreversible up to 6W after cessation of ozone exposure, and were not reversed by NAC. The beneficial effects of therapeutic NAC may be restricted to the ASM.

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  • Rodent studies confirmed that the use of N-acetylcysteine and sulfide salt can help prevent or recover the lung impairment caused by ozone.

    “For example, rodent studies confirmed that the use of N-acetylcysteine and sulfide salt can help prevent or recover the lung impairment caused by ozone (82, 83).”

    From Ozone pollution: A Major health hazard worldwide (2019) · cites this paper as [83]

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Authors
Li, F., Wiegman, C., Seiffert, J. M., Zhu, J., Clarke, C., Chang, Y., Bhavsar, P., Adcock, I., Zhang, J., Zhou, X., & Chung, K. F.
Affiliations
  • Shanghai Jiao Tong University (CN)
  • Imperial College London (GB)
  • University of Southern California (US)
Corresponding author
Chung, Kian Fan
Venue
PLoS ONE
Published
2013-11-18
Volume
8
Issue
11
Pages
e80782
ISSN
1932-6203 (ISSN-L)
OpenAlex
W2014519750
Cited by
62
References
29
Citations by year
2026: 1 · 2025: 4 · 2024: 5 · 2023: 7 · 2022: 5 · 2021: 9 · 2020: 6 · 2019: 4 · 2018: 6 · 2017: 7 · 2016: 5 · 2015: 2 · 2014: 1
FWCI
2.17
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
  • Figshare (submittedVersion, cc-by)
  • Spiral (Imperial College London) (submittedVersion, other-oa)
Funders
  • European Respiratory Society
  • Wellcome Trust (083905)
  • Lloyd's Tercentenary Research Foundation
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
  • Health Sciences › Medicine › Physiology › Asthma and respiratory diseases
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Air Quality and Health Impacts
Keywords
N-acetylcysteine, ozone exposure, chronic obstructive pulmonary disease, emphysema, airway hyperresponsiveness, airway smooth muscle, lung function, macrophages, apoptosis, antioxidant therapy, chronic inflammation
MeSH terms
8-Hydroxy-2'-Deoxyguanosine, Acetylcysteine, Animals, Bronchoalveolar Lavage Fluid, Deoxyguanosine, Disease Models, Animal, Emphysema, Expectorants, Lung, Malondialdehyde, Ozone, Respiratory Function Tests, Gene Expression, Bronchial Hyperreactivity, Apoptosis, Pulmonary Disease, Chronic Obstructive, Mice

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