Pulmonary Immune Response Regulation, Genotoxicity, and Metabolic Reprogramming by Menthol and Tobacco Flavored E-Cigarette Exposures in Mice.
Thivanka MuthumalageIrfan RahmanPublished in: Toxicological sciences : an official journal of the Society of Toxicology (2023)
Menthol and tobacco flavors are available for almost all tobacco products, including electronic cigarettes (e-cigs). These flavors are a mixture of chemicals with overlapping constituents. There are no comparative toxicity studies of these flavors produced by different manufacturers. We hypothesized that acute exposure to menthol and tobacco-flavored e-cig aerosols induces inflammatory, genotoxicity, and metabolic responses in mouse lungs. We compared two brands, A and B, e-cig flavors (PG/VG, menthol, and tobacco) with and without nicotine for their inflammatory response, genotoxic markers, altered genes and proteins in the context of metabolism by exposing mouse strains, C57BL/6J (Th1-mediated) and BALB/cJ (Th2-mediated). Brand A nicotine-free menthol exposure caused increased neutrophils and differential T-lymphocyte influx in bronchoalveolar lavage fluid (BALF) and induced significant immunosuppression, while brand A tobacco with nicotine elicited an allergic inflammatory response with increased Eotaxin, IL-6, and RANTES levels. Brand B elicited a similar inflammatory response in menthol flavor exposure. Upon e-cig exposure, genotoxicity markers, significantly increased in lung tissue. These inflammatory and genotoxicity responses were associated with altered NLRP3 inflammasome and TRPA1 induction by menthol flavor. Nicotine decreased surfactant protein D and increased PAI-1 by menthol and tobacco flavors, respectively. Integration of inflammatory and metabolic pathway gene expression analysis showed immunometabolic regulation in T-cells via PI3K/Akt/p70S6k-mTOR axis associated with suppressed immunity/allergic immune response. Overall, this study showed comparative toxicity of flavored e-cig aerosols, unraveling potential signaling pathways of nicotine and flavor-mediated pulmonary toxicological responses, and emphasized the need for standardized toxicity testing for appropriate premarket authorization of e-cigarette products.
Keyphrases
- cell cycle arrest
- pi k akt
- smoking cessation
- inflammatory response
- signaling pathway
- immune response
- cell proliferation
- oxidative stress
- oxide nanoparticles
- nlrp inflammasome
- pulmonary hypertension
- replacement therapy
- toll like receptor
- adipose tissue
- genome wide identification
- escherichia coli
- liver failure
- genome wide
- dna methylation
- risk assessment
- intensive care unit
- induced apoptosis
- amino acid
- metabolic syndrome
- drug induced
- water soluble
- respiratory failure
- dendritic cells
- aortic dissection
- wild type