Ramenzoni Liza L, Schneider Andreas, Fox Stephan C, Meyer Michael, Meboldt Mirko, Attin Thomas, Schmidlin Patrick R
Clinic of Conservative and Preventive Dentistry, Center of Dental Medicine, University of Zurich, 8032 Zurich, Switzerland.
Product Development Group Zurich, Material and Fabrication, Department of Mechanical and Process Engineering, Swiss Federal Institute of Technology Zurich, 8032 Zurich, Switzerland.
Toxics. 2022 Apr 6;10(4):179. doi: 10.3390/toxics10040179.
Information about the potential oral health effects of vaping from electronic cigarettes (e-cigs) is still sparse and inconsistent. The purpose of this study was to compare the safety and cytotoxicity of e-cig liquid aerosols versus traditional cigarette (t-cig) smoke on human epithelial oral cells. T-cig smoke and e-cig aerosols were generated by a newly developed automated smoking instrument in order to simulate realistic user puffing behaviors. Air−liquid interface transwell cell cultures were exposed to standardized puff topography (puff duration: 2 s, puff volume: 35 mL, puff frequency: 1 puff every 60 s) of reference t-cigs or commercially available e-cigs at different air dilutions. Cell viability, morphology, and death rate were evaluated with MTT and TUNEL assays. The inflammatory cytokine gene expression of inflammatory genes was assessed by quantitative RT-PCR. E-cigs and t-cigs indicated similar adverse effects by enhancing cytotoxicity and cell death in a dose-dependent manner. E-cig aerosol and t-cig smoke treatment expressed upregulation of inflammatory cytokines up to 3.0-fold (p < 0.05). These results indicate that e-cig smoking may contribute to oral tissue−cell damage and tissue inflammation. Our approach allows the production of e-cig aerosol and t-cig smoke in order to identify harmful effects in oral tissues in vitro.
关于电子烟吸雾对口腔健康的潜在影响的信息仍然稀少且不一致。本研究的目的是比较电子烟液体气溶胶与传统香烟烟雾对人口腔上皮细胞的安全性和细胞毒性。通过一种新开发的自动吸烟仪器产生传统香烟烟雾和电子烟气溶胶,以模拟实际使用者的抽吸行为。将气液界面Transwell细胞培养物暴露于不同空气稀释度下的参考传统香烟或市售电子烟的标准化抽吸形貌(抽吸持续时间:2秒,抽吸体积:35毫升,抽吸频率:每60秒1次抽吸)。用MTT和TUNEL试验评估细胞活力、形态和死亡率。通过定量RT-PCR评估炎症基因的炎性细胞因子基因表达。电子烟和传统香烟通过以剂量依赖方式增强细胞毒性和细胞死亡显示出相似的不良影响。电子烟气溶胶和传统香烟烟雾处理使炎性细胞因子表达上调高达3.0倍(p<0.05)。这些结果表明,吸电子烟可能导致口腔组织细胞损伤和组织炎症。我们的方法能够产生电子烟气溶胶和传统香烟烟雾,以便在体外识别口腔组织中的有害影响。