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In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung

Background: The developing lung is uniquely susceptible and may be at increased risk of injury with exposure to e-cigarette constituents. We hypothesize that cellular toxicity and airway and vascular responses with exposure to flavored refill solutions may be altered in the immature lung. Methods: F...

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Autores principales: Berkelhamer, Sara K., Helman, Justin M., Gugino, Sylvia F., Leigh, Noel J., Lakshminrusimha, Satyan, Goniewicz, Maciej L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801380/
https://www.ncbi.nlm.nih.gov/pubmed/31569724
http://dx.doi.org/10.3390/ijerph16193635
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author Berkelhamer, Sara K.
Helman, Justin M.
Gugino, Sylvia F.
Leigh, Noel J.
Lakshminrusimha, Satyan
Goniewicz, Maciej L.
author_facet Berkelhamer, Sara K.
Helman, Justin M.
Gugino, Sylvia F.
Leigh, Noel J.
Lakshminrusimha, Satyan
Goniewicz, Maciej L.
author_sort Berkelhamer, Sara K.
collection PubMed
description Background: The developing lung is uniquely susceptible and may be at increased risk of injury with exposure to e-cigarette constituents. We hypothesize that cellular toxicity and airway and vascular responses with exposure to flavored refill solutions may be altered in the immature lung. Methods: Fetal, neonatal, and adult ovine pulmonary artery smooth muscle cells (PASMC) were exposed to popular flavored nicotine-free e-cigarette refill solutions (menthol, strawberry, tobacco, and vanilla) and unflavored solvents: propylene glycol (PG) or vegetable glycerin (VG). Viability was assessed by lactate dehydrogenase assay. Brochodilation and vasoreactivity were determined on isolated ovine bronchial rings (BR) and pulmonary arteries (PA). Results: Neither PG or VG impacted viability of immature or adult cells; however, exposure to menthol and strawberry flavored solutions increased cell death. Neonatal cells were uniquely susceptible to menthol flavoring-induced toxicity, and all four flavorings demonstrated lower lethal doses (LD50) in immature PASMC. Exposure to flavored solutions induced bronchodilation of neonatal BR, while only menthol induced airway relaxation in adults. In contrast, PG/VG and flavored solutions did not impact vasoreactivity with the exception of menthol-induced relaxation of adult PAs. Conclusion: The immature lung is uniquely susceptible to cellular toxicity and altered airway responses with exposure to common flavored e-cigarette solutions.
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spelling pubmed-68013802019-10-31 In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung Berkelhamer, Sara K. Helman, Justin M. Gugino, Sylvia F. Leigh, Noel J. Lakshminrusimha, Satyan Goniewicz, Maciej L. Int J Environ Res Public Health Article Background: The developing lung is uniquely susceptible and may be at increased risk of injury with exposure to e-cigarette constituents. We hypothesize that cellular toxicity and airway and vascular responses with exposure to flavored refill solutions may be altered in the immature lung. Methods: Fetal, neonatal, and adult ovine pulmonary artery smooth muscle cells (PASMC) were exposed to popular flavored nicotine-free e-cigarette refill solutions (menthol, strawberry, tobacco, and vanilla) and unflavored solvents: propylene glycol (PG) or vegetable glycerin (VG). Viability was assessed by lactate dehydrogenase assay. Brochodilation and vasoreactivity were determined on isolated ovine bronchial rings (BR) and pulmonary arteries (PA). Results: Neither PG or VG impacted viability of immature or adult cells; however, exposure to menthol and strawberry flavored solutions increased cell death. Neonatal cells were uniquely susceptible to menthol flavoring-induced toxicity, and all four flavorings demonstrated lower lethal doses (LD50) in immature PASMC. Exposure to flavored solutions induced bronchodilation of neonatal BR, while only menthol induced airway relaxation in adults. In contrast, PG/VG and flavored solutions did not impact vasoreactivity with the exception of menthol-induced relaxation of adult PAs. Conclusion: The immature lung is uniquely susceptible to cellular toxicity and altered airway responses with exposure to common flavored e-cigarette solutions. MDPI 2019-09-27 2019-10 /pmc/articles/PMC6801380/ /pubmed/31569724 http://dx.doi.org/10.3390/ijerph16193635 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Berkelhamer, Sara K.
Helman, Justin M.
Gugino, Sylvia F.
Leigh, Noel J.
Lakshminrusimha, Satyan
Goniewicz, Maciej L.
In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title_full In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title_fullStr In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title_full_unstemmed In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title_short In Vitro Consequences of Electronic-Cigarette Flavoring Exposure on the Immature Lung
title_sort in vitro consequences of electronic-cigarette flavoring exposure on the immature lung
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801380/
https://www.ncbi.nlm.nih.gov/pubmed/31569724
http://dx.doi.org/10.3390/ijerph16193635
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