Pleiss K L, Mosley D D, Bauer C D, Bailey K L, Ochoa C A, Knoell D L, Wyatt T A
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, United States.
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, College of Medicine, University of Nebraska Medical Center, Omaha, NE, United States; Veterans Affairs Nebraska-Western Iowa Health Care System, Omaha, NE, United States.
Toxicol Lett. 2025 May 1;407:32-40. doi: 10.1016/j.toxlet.2025.03.003. Epub 2025 Mar 16.
Because of cigarette smoking, chronic lung diseases are the third leading cause of death in the United States. Electronic cigarettes (e-cig) were originally marketed as harm reduction devices for cigarette smokers due to low success rates with traditional smoking cessation methods. While several studies show that cigarette smoke causes damage to the lungs, comparative research assessing the injury profile of e-cig to traditional cigarettes is still limited. Comparative lung injury studies are crucial in determining the validity of e-cig as a harm reduction device for chronic smokers and can be used to assess the quality of alternate nicotine delivery options to reduce the morbidity and mortality caused by cigarettes. We hypothesize that exposure to JUUL to e-cig vapor produces decreased in vitro markers of lung injury in comparison to cigarette smoke extract at equivalent and higher nicotine concentrations to that from CSE. We compared the extent of injury to airway epithelial tissue from cigarettes and e-cig using various assays of cellular function, including ciliary beat frequency (CBF), wound closure, barrier function, cytokine release, and kinase activity. Cells were treated with various concentrations of Virginia Tobacco-flavored JUUL™ vapor extract (JVE) and cigarette smoke extract (CSE) either normalized for nicotine concentration or equivalent % dilutions from a 100 % stock extract. CSE stimulated cilia in the short term, but slowed cilia after several hours of exposure, whereas cells treated with JVE showed no significant changes in CBF. CSE slowed wound repair, but nicotine-equivalent doses of JVE did not significantly slow wound repair. CSE increased epithelial cell monolayer permeability and interleukin release in a concentration-dependent manner, but these were not observed with JVE treatment. Kinase activity assays revealed activation translocation of protein kinase C (PKC) activity in cells treated with CSE, but no such change in PKC activity was observed in JVE groups. The results of these in vitro assays suggest that at nicotine-equivalent doses, JVE from Virginia Tobacco-flavored JUUL does not impact the airway epithelium in the same manner as CSE. The lack of evidence for in vitro tissue injury in this study caused by JUUL™ vapor extract is not a justification for the harm posed by nicotine addiction, particularly at the high levels of nicotine contained in these products which are several times the legal limit of many countries.
由于吸烟,慢性肺病是美国第三大死因。电子烟最初作为传统戒烟方法成功率较低的情况下,为吸烟者减少危害的设备进行销售。虽然多项研究表明香烟烟雾会对肺部造成损害,但评估电子烟与传统香烟损伤情况的对比研究仍然有限。肺部损伤对比研究对于确定电子烟作为慢性吸烟者减少危害设备的有效性至关重要,并且可用于评估替代尼古丁递送选项的质量,以降低香烟导致的发病率和死亡率。我们假设,与等效及更高尼古丁浓度的香烟烟雾提取物相比,暴露于JUUL电子烟蒸汽会使体外肺损伤标志物减少。我们使用多种细胞功能检测方法,包括纤毛摆动频率(CBF)、伤口闭合、屏障功能、细胞因子释放和激酶活性,比较了香烟和电子烟对气道上皮组织的损伤程度。细胞用不同浓度的弗吉尼亚烟草味JUUL™蒸汽提取物(JVE)和香烟烟雾提取物(CSE)处理,CSE要么按尼古丁浓度标准化,要么从100%原液提取物进行等效百分比稀释。CSE在短期内刺激纤毛,但暴露数小时后会减缓纤毛运动,而用JVE处理的细胞CBF没有显著变化。CSE减缓伤口修复,但尼古丁等效剂量的JVE没有显著减缓伤口修复。CSE以浓度依赖方式增加上皮细胞单层通透性和白细胞介素释放,但JVE处理未观察到这些情况。激酶活性检测显示,用CSE处理的细胞中蛋白激酶C(PKC)活性发生激活易位,但JVE组未观察到PKC活性有此类变化。这些体外检测结果表明,在尼古丁等效剂量下,弗吉尼亚烟草味JUUL的JVE对气道上皮的影响与CSE不同。本研究中缺乏JUUL™蒸汽提取物导致体外组织损伤的证据,并非尼古丁成瘾危害的正当理由,特别是这些产品中所含尼古丁水平很高,是许多国家法定限量的数倍。