Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models

Abstract Limited toxicity data on electronic cigarette (ECIG) impede evidence-based policy recommendations. We compared two popular mixed fruit flavored ECIG-liquids with and without nicotine aerosolized at 40 W (E-smoke) with respect to particle number concentrations, chemical composition, and resp...

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Autores principales: Koustav Ganguly, Axel Nordström, Tania A. Thimraj, Mizanur Rahman, Malin Ramström, Shanzina I. Sompa, Elizabeth Z. Lin, Fiona O’Brien, Jeremy Koelmel, Lena Ernstgård, Gunnar Johanson, Krystal J. Godri Pollitt, Lena Palmberg, Swapna Upadhyay
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Publicado: Nature Portfolio 2020
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spelling oai:doaj.org-article:cd03240c31f6416eae94feae916263532021-12-02T16:08:46ZAddressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models10.1038/s41598-020-77452-w2045-2322https://doaj.org/article/cd03240c31f6416eae94feae916263532020-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-77452-whttps://doaj.org/toc/2045-2322Abstract Limited toxicity data on electronic cigarette (ECIG) impede evidence-based policy recommendations. We compared two popular mixed fruit flavored ECIG-liquids with and without nicotine aerosolized at 40 W (E-smoke) with respect to particle number concentrations, chemical composition, and response on physiologically relevant human bronchial and alveolar lung mucosa models cultured at air–liquid interface. E-smoke was characterized by significantly increased particle number concentrations with increased wattage (25, 40, and 55 W) and nicotine presence. The chemical composition of E-smoke differed across the two tested flavors in terms of cytotoxic compounds including p-benzoquinone, nicotyrine, and flavoring agents (for example vanillin, ethyl vanillin). Significant differences in the expression of markers for pro-inflammation, oxidative stress, tissue injury/repair, alarm anti-protease, anti-microbial defense, epithelial barrier function, and epigenetic modification were observed between the flavors, nicotine content, and/ or lung models (bronchial or alveolar). Our findings indicate that ECIG toxicity is influenced by combination of multiple factors including flavor, nicotine content, vaping regime, and the region of respiratory tree (bronchial or alveolar). Toxic chemicals and flavoring agents detected in high concentrations in the E-smoke of each flavor warrant independent evaluation for their specific role in imparting toxicity. Therefore, multi-disciplinary approaches are warranted for comprehensive safety profiling of ECIG.Koustav GangulyAxel NordströmTania A. ThimrajMizanur RahmanMalin RamströmShanzina I. SompaElizabeth Z. LinFiona O’BrienJeremy KoelmelLena ErnstgårdGunnar JohansonKrystal J. Godri PollittLena PalmbergSwapna UpadhyayNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-15 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Koustav Ganguly
Axel Nordström
Tania A. Thimraj
Mizanur Rahman
Malin Ramström
Shanzina I. Sompa
Elizabeth Z. Lin
Fiona O’Brien
Jeremy Koelmel
Lena Ernstgård
Gunnar Johanson
Krystal J. Godri Pollitt
Lena Palmberg
Swapna Upadhyay
Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
description Abstract Limited toxicity data on electronic cigarette (ECIG) impede evidence-based policy recommendations. We compared two popular mixed fruit flavored ECIG-liquids with and without nicotine aerosolized at 40 W (E-smoke) with respect to particle number concentrations, chemical composition, and response on physiologically relevant human bronchial and alveolar lung mucosa models cultured at air–liquid interface. E-smoke was characterized by significantly increased particle number concentrations with increased wattage (25, 40, and 55 W) and nicotine presence. The chemical composition of E-smoke differed across the two tested flavors in terms of cytotoxic compounds including p-benzoquinone, nicotyrine, and flavoring agents (for example vanillin, ethyl vanillin). Significant differences in the expression of markers for pro-inflammation, oxidative stress, tissue injury/repair, alarm anti-protease, anti-microbial defense, epithelial barrier function, and epigenetic modification were observed between the flavors, nicotine content, and/ or lung models (bronchial or alveolar). Our findings indicate that ECIG toxicity is influenced by combination of multiple factors including flavor, nicotine content, vaping regime, and the region of respiratory tree (bronchial or alveolar). Toxic chemicals and flavoring agents detected in high concentrations in the E-smoke of each flavor warrant independent evaluation for their specific role in imparting toxicity. Therefore, multi-disciplinary approaches are warranted for comprehensive safety profiling of ECIG.
format article
author Koustav Ganguly
Axel Nordström
Tania A. Thimraj
Mizanur Rahman
Malin Ramström
Shanzina I. Sompa
Elizabeth Z. Lin
Fiona O’Brien
Jeremy Koelmel
Lena Ernstgård
Gunnar Johanson
Krystal J. Godri Pollitt
Lena Palmberg
Swapna Upadhyay
author_facet Koustav Ganguly
Axel Nordström
Tania A. Thimraj
Mizanur Rahman
Malin Ramström
Shanzina I. Sompa
Elizabeth Z. Lin
Fiona O’Brien
Jeremy Koelmel
Lena Ernstgård
Gunnar Johanson
Krystal J. Godri Pollitt
Lena Palmberg
Swapna Upadhyay
author_sort Koustav Ganguly
title Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
title_short Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
title_full Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
title_fullStr Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
title_full_unstemmed Addressing the challenges of E-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
title_sort addressing the challenges of e-cigarette safety profiling by assessment of pulmonary toxicological response in bronchial and alveolar mucosa models
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/cd03240c31f6416eae94feae91626353
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