Time course of changes in inflammatory and oxidative biomarkers in lung tissue of mice induced by exposure to electronic cigarette aerosol

Abstract

Significance: Electronic cigarettes (e-cigarettes) have become a popular way to smoke all over the world. Chronic exposure to e-cigarette aerosol may influence lung health. This study uses an animal model to explore the time course of the effect of exposure to e-cigarette aerosols on the lung. Methods: Lung samples were collected after exposure of Balb/c mice to e-cigarette aerosols for 1 h/day (6 times/week) for 1, 2 and 4 weeks and compared to sham-exposed controls. Examined biomarkers including inflammatory cells, tumor necrosis factor α (TNFα), interleukin-6 (IL-6), interleukin-10 (IL-10), reduced glutathione (GSH), oxidized glutathione (GSSG), glutathione peroxidase (GPx), catalase, superoxide dismutase (SOD), and Thiobarbituric acid reactive substances (TBARS). Results: Exposure of animals to e-cigarette aerosols induced significant increases (P < 0.05) in total inflammatory cells, eosinophils, macrophages and TNFα in the lung tissue after 1, 2 and 4 weeks of exposure. Furthermore, level of IL-10 significantly decreased, whereas levels of neutrophils and basophils significantly increased (P < 0.05) after 1 week of exposure. Exposure of animals to e-cigarette aerosol also induced significant decreases (P < 0.05) in the GSH/GSSG ratio, and GPx levels after 2 and 4 weeks of exposures. The activity of catalase was also reduced (P < 0.05) after 4 weeks of exposure. Level of TBARS showed a trend of elevation with time and it reached a significant elevation after 4 weeks (P < 0.01). Conclusion: Current results indicate that inhalation of unflavored e-cigarette aerosol might be associated with inflammation in lung tissue that worsen as the duration of exposure increases. Further experiments including more time points, histopathology and pulmonary physiology experiments are needed to confirm the current results. © 2022 The Authors

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Keywords

Aerosol, E-cigarettes, Il-10, Il-6, Lung, Tnfα, Biological marker, Catalase, Glutathione disulfide, Glutathione peroxidase, Interleukin 10, Interleukin 6, Ketamine, Nitric oxide, Tumor necrosis factor, Animal experiment, Animal model, Animal tissue, Article, Bagg albino mouse, Biochemical analysis, Bronchoalveolar lavage fluid, Enzyme activity, Enzyme linked immunosorbent assay, Eosinophil, Forced vital capacity, Gene expression, Histopathology, Inflammatory cell, Inhalation, Leukocyte differential count, Lipid peroxidation, Lung parenchyma, Macrophage, Male, Mouse, Neutrophil, Nonhuman, Oxidation, Oxidative stress, Particulate matter, Pneumonia, Protein expression, Smoking, Smoking cessation

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