The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice
Electronic cigarette usage is increasing worldwide, yet there is a paucity of information on the respiratory health effects of electronic cigarette aerosol exposure. This study aimed to assess whether exposure to electronic cigarette (e-cigarette) aerosol would alter lung function and pulmonary infl...
| Main Authors: | , , , , , |
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| Format: | Journal Article |
| Published: |
American Physiological Society
2017
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| Online Access: | http://hdl.handle.net/20.500.11937/70080 |
| _version_ | 1848762209499348992 |
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| author | Larcombe, Alexander Janka, M. Mullins, Ben Berry, L. Bredin, Arne Franklin, P. |
| author_facet | Larcombe, Alexander Janka, M. Mullins, Ben Berry, L. Bredin, Arne Franklin, P. |
| author_sort | Larcombe, Alexander |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | Electronic cigarette usage is increasing worldwide, yet there is a paucity of information on the respiratory health effects of electronic cigarette aerosol exposure. This study aimed to assess whether exposure to electronic cigarette (e-cigarette) aerosol would alter lung function and pulmonary inflammation in mice and to compare the severity of any alterations with mice exposed to mainstream tobacco smoke. Female BALB/c mice were exposed for 8 wk to tobacco smoke, medical air (control), or one of four different types of e-cigarette aerosol. E-cigarette aerosols varied depending on nicotine content (0 or 12 mg/ml) and the main excipient (propylene glycol or glycerin). Twenty-four hours after the final exposure, we measured pulmonary inflammation, lung volume lung mechanics, and responsiveness to methacholine. Mice exposed to tobacco cigarette smoke had increased pulmonary inflammation and responsiveness to methacholine compared with air controls. Mice exposed to e-cigarette aerosol did not have increased inflammation but did display decrements in parenchymal lung function at both functional residual capacity and high transrespiratory pressures. Mice exposed to glycerin-based e-cigarette aerosols were also hyperresponsive to methacholine regardless of the presence or absence of nicotine. This study shows, for the first time, that exposure to e-cigarette aerosol during adolescence and early adulthood is not harmless to the lungs and can result in significant impairments in lung function. |
| first_indexed | 2025-11-14T10:43:56Z |
| format | Journal Article |
| id | curtin-20.500.11937-70080 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T10:43:56Z |
| publishDate | 2017 |
| publisher | American Physiological Society |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-700802018-10-11T07:06:16Z The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice Larcombe, Alexander Janka, M. Mullins, Ben Berry, L. Bredin, Arne Franklin, P. Electronic cigarette usage is increasing worldwide, yet there is a paucity of information on the respiratory health effects of electronic cigarette aerosol exposure. This study aimed to assess whether exposure to electronic cigarette (e-cigarette) aerosol would alter lung function and pulmonary inflammation in mice and to compare the severity of any alterations with mice exposed to mainstream tobacco smoke. Female BALB/c mice were exposed for 8 wk to tobacco smoke, medical air (control), or one of four different types of e-cigarette aerosol. E-cigarette aerosols varied depending on nicotine content (0 or 12 mg/ml) and the main excipient (propylene glycol or glycerin). Twenty-four hours after the final exposure, we measured pulmonary inflammation, lung volume lung mechanics, and responsiveness to methacholine. Mice exposed to tobacco cigarette smoke had increased pulmonary inflammation and responsiveness to methacholine compared with air controls. Mice exposed to e-cigarette aerosol did not have increased inflammation but did display decrements in parenchymal lung function at both functional residual capacity and high transrespiratory pressures. Mice exposed to glycerin-based e-cigarette aerosols were also hyperresponsive to methacholine regardless of the presence or absence of nicotine. This study shows, for the first time, that exposure to e-cigarette aerosol during adolescence and early adulthood is not harmless to the lungs and can result in significant impairments in lung function. 2017 Journal Article http://hdl.handle.net/20.500.11937/70080 10.1152/ajplung.00203.2016 American Physiological Society restricted |
| spellingShingle | Larcombe, Alexander Janka, M. Mullins, Ben Berry, L. Bredin, Arne Franklin, P. The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title | The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title_full | The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title_fullStr | The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title_full_unstemmed | The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title_short | The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| title_sort | effects of electronic cigarette aerosol exposure on inflammation and lung function in mice |
| url | http://hdl.handle.net/20.500.11937/70080 |