Lee K Monica, Hoeng Julia, Harbo Sam, Kogel Ulrike, Gardner William, Oldham Michael, Benson Eric, Talikka Marja, Kondylis Athanasios, Martin Florian, Titz Bjoern, Ansari Sam, Trivedi Keyur, Guedj Emmanuel, Elamin Ashraf, Ivanov Nikolai V, Vanscheeuwijck Patrick, Peitsch Manuel C, McKinney Willie J
a Altria Client Services LLC , Richmond , VA , USA.
b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Inhal Toxicol. 2018 Nov-Dec;30(13-14):553-567. doi: 10.1080/08958378.2019.1576807. Epub 2019 Mar 8.
We compared early biological changes in mice after inhalation exposures to cigarette smoke or e-vapor aerosols (MarkTen cartridge with Carrier, Test-1, or Test-2 formulations; 4% nicotine). Female C57BL/6 mice were exposed to 3R4F cigarette smoke or e-vapor aerosols by nose-only inhalation for up to 4 hours/day, 5 days/week, for 3 weeks. The 3R4F and e-vapor exposures were set to match the target nose port aerosol nicotine concentration (∼41 µg/L). Only the 3R4F group showed postexposure clinical signs such as tremors and lethargy. At necropsy, the 3R4F group had significant increases in lung weight and changes in bronchoalveolar lavage parameters, as well as microscopic findings in the respiratory tract. The e-vapor groups had minimal microscopic changes, including squamous metaplasia in laryngeal epiglottis, and histiocytic infiltrates in the lung (Test-2 group only). The 3R4F group had a higher incidence and severity of microscopic findings compared to any e-vapor group. Transcriptomic analysis also showed that the 3R4F group had the highest number of differentially expressed genes compared to Sham Control. Among e-vapor groups, Test-2 group had more differentially expressed genes but the magnitude of gene expression-based network perturbations in all e-vapor groups was ∼94% less than the 3R4F group. On proteome analysis in the lung, differentially regulated proteins were detected in the 3R4F group only. In conclusion, 3-weeks of 3R4F exposure induced molecular and microscopic changes associated with smoking-related diseases in the respiratory tract, while e-vapor exposures showed substantially reduced biological activities.
我们比较了小鼠吸入香烟烟雾或电子烟烟雾(MarkTen烟弹搭配载体、测试-1或测试-2配方;4%尼古丁)后的早期生物学变化。雌性C57BL/6小鼠通过仅经鼻吸入暴露于3R4F香烟烟雾或电子烟烟雾中,每天最多4小时,每周5天,持续3周。3R4F和电子烟暴露的设置是为了使目标鼻端口气溶胶尼古丁浓度(约41μg/L)相匹配。只有3R4F组在暴露后出现了诸如震颤和嗜睡等临床症状。尸检时,3R4F组的肺重量显著增加,支气管肺泡灌洗参数发生变化,呼吸道也有微观发现。电子烟组的微观变化最小,包括喉会厌的鳞状化生,以及肺中的组织细胞浸润(仅测试-2组)。与任何电子烟组相比,3R4F组微观发现的发生率和严重程度更高。转录组分析还表明,与假手术对照组相比,3R4F组差异表达基因的数量最多。在电子烟组中,测试-2组的差异表达基因更多,但所有电子烟组基于基因表达的网络扰动程度比3R4F组低约94%。在肺的蛋白质组分析中,仅在3R4F组中检测到差异调节的蛋白质。总之,3周的3R4F暴露诱导了与呼吸道吸烟相关疾病相关的分子和微观变化,而电子烟暴露显示出生物活性大幅降低。