Correia-Álvarez Eva, Keating James E, Glish Gary, Tarran Robert, Sassano M Flori
Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC.
Department of Chemistry, University of North Carolina, Chapel Hill, NC.
Nicotine Tob Res. 2020 Dec 15;22(Suppl 1):S4-S13. doi: 10.1093/ntr/ntaa177.
The use of flavors in electronic cigarettes appeals to adults and never-smoking youth. Consumption has rapidly increased over the last decade, and in the U.S. market alone, there are over 8000 unique flavors. The U.S. Food and Drug Administration (FDA) has begun to regulate e-liquids, but many have not been tested, and their impact, both at the cellular level, and on human health remains unclear.
We tested e-liquids on the human cell line HEK293T and measured toxicity, mitochondrial membrane potential (ΔΨ m), reactive oxygen species production (ROS), and cellular membrane potential (Vm) using high-throughput screening (HTS) approaches. Our HTS efforts included single-dose and 16-point dose-response curves, which allowed testing of ≥90 commercially available e-liquids in parallel to provide a rapid assessment of cellular effects as a proof of concept for a fast, preliminary toxicity method. We also investigated the chemical composition of the flavors via gas chromatography-mass spectrometry.
We found that e-liquids caused a decrease in ΔΨ m and Vm and an increase in ROS production and toxicity in a dose-dependent fashion. In addition, the presence of five specific chemical components: vanillin, benzyl alcohol, acetoin, cinnamaldehyde, and methyl-cyclopentenolone, but not nicotine, were linked with the changes observed in the cellular traits studied.
Our data suggest that ΔΨ m, ROS, Vm, and toxicity may be indicative of the extent of cell death upon e-liquid exposure. Further research on the effect of flavors should be prioritized to help policy makers such as the FDA to regulate e-liquid composition.
E-liquid cellular toxicity can be predicted using parameters amenable to HTS. Our data suggest that ΔΨ m, ROS, Vm, and toxicity may be indicative of the extent of cell death upon e-liquid exposure, and this toxicity is linked to the chemical composition, that is, flavoring components. Further research on the effect of flavors should be prioritized to help policy makers such as the FDA to regulate e-liquid composition.
电子烟中香料的使用吸引了成年人和从不吸烟的青少年。在过去十年中,电子烟的消费量迅速增加,仅在美国市场,就有超过8000种独特的香料。美国食品药品监督管理局(FDA)已开始对电子烟液进行监管,但许多产品尚未经过测试,其在细胞水平以及对人体健康的影响仍不明确。
我们在人类细胞系HEK293T上测试了电子烟液,并使用高通量筛选(HTS)方法测量了毒性、线粒体膜电位(ΔΨm)、活性氧生成(ROS)和细胞膜电位(Vm)。我们的高通量筛选工作包括单剂量和16点剂量反应曲线,这使得能够并行测试≥90种市售电子烟液,以便快速评估细胞效应,作为一种快速、初步毒性方法的概念验证。我们还通过气相色谱-质谱法研究了香料的化学成分。
我们发现电子烟液会导致ΔΨm和Vm降低,ROS生成和毒性呈剂量依赖性增加。此外,五种特定化学成分:香草醛、苯甲醇、乙偶姻、肉桂醛和甲基环戊烯醇酮的存在,但不是尼古丁,与所研究的细胞特征变化有关。
我们的数据表明,ΔΨm、ROS、Vm和毒性可能表明电子烟液暴露后细胞死亡的程度。应优先对香料的影响进行进一步研究,以帮助FDA等政策制定者规范电子烟液成分。
可以使用适用于高通量筛选的参数来预测电子烟液的细胞毒性。我们的数据表明,ΔΨm、ROS、Vm和毒性可能表明电子烟液暴露后细胞死亡的程度,并且这种毒性与化学成分,即调味成分有关。应优先对香料的影响进行进一步研究,以帮助FDA等政策制定者规范电子烟液成分。