Flavored e-cigarette liquids reduce proliferation and viability in the CALU3 airway epithelial cell line

被引:92
作者
Rowell, Temperance R. [1 ,2 ]
Reeber, Steven L. [3 ]
Lee, Shernita L. [2 ]
Harris, Rachel A. [3 ]
Nethery, Rachel C. [4 ]
Herring, Amy H. [4 ]
Glish, Gary L. [3 ]
Tarran, Robert [1 ,2 ]
机构
[1] Univ N Carolina, Marsico Lung Inst, Chapel Hill, NC USA
[2] Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC USA
[3] Univ N Carolina, Dept Chem, Chapel Hill, NC USA
[4] Univ N Carolina, Dept Biostat, Gillings Sch Global Publ Hlth, Chapel Hill, NC USA
关键词
tobacco; COPD; cancer; nicotine; aerosols; NICOTINIC ACETYLCHOLINE-RECEPTORS; ELECTRONIC CIGARETTES; AEROSOL; EXPOSURE; DEPOSITION; EXPRESSION; BRONCHIOLITIS; CHEMICALS; SMOKERS; MODELS;
D O I
10.1152/ajplung.00392.2016
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
E-cigarettes are generally thought of as a safer smoking alternative to traditional cigarettes. However, little is known about the effects of e-cigarette liquids (e-liquids) on the lung. Since over 7,000 unique flavors have been identified for purchase in the United States, our goal was to conduct a screen that would test whether different flavored e-liquids exhibited different toxicant profiles. We tested the effects of 13 different flavored e-liquids [with nicotine and propylene glycol/vegetable glycerin (PG/VG) serving as controls] on a lung epithelial cell line (CALU3). Using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay as an indicator of cell proliferation/viability, we demonstrated a dose-dependent decrease of MTT metabolism by all flavors tested. However, a group of four flavors consistently showed significantly greater toxicity compared with the PG/VG control, indicating the potential for some flavors to elicit more harmful effects than others. We also tested the aerosolized "vapor" from select e-liquids on cells and found similar dose-dependent trends, suggesting that direct e-liquid exposures are a justifiable first-pass screening approach for determining relative e-liquid toxicity. We then identified individual chemical constituents for all 13 flavors using gas chromatography-mass spectrometry. These data revealed that beyond nicotine and PG/VG, the 13 flavored e-liquids have diverse chemical constituents. Since all of the flavors exhibited some degree of toxicity and a diverse array of chemical constituents with little inhalation toxicity available, we conclude that flavored e-liquids should be extensively tested on a case-by-case basis to determine the potential for toxicity in the lung and elsewhere.
引用
收藏
页码:L52 / L66
页数:15
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