| Autor: |
Day NJ; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., Wang J; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., Johnston CJ; Division of Pulmonology, Department of Pediatric Pulmonology, University of Rochester Medical Center, Rochester, New York, United States.; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, United States., Kim SY; Division of Pulmonology, Department of Pediatric Pulmonology, University of Rochester Medical Center, Rochester, New York, United States.; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, United States., Olson HM; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., House EL; Division of Pulmonology, Department of Pediatric Pulmonology, University of Rochester Medical Center, Rochester, New York, United States.; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, United States., Attah IK; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., Clair GC; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., Qian WJ; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States., McGraw MD; Division of Pulmonology, Department of Pediatric Pulmonology, University of Rochester Medical Center, Rochester, New York, United States.; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, United States. |
| Abstrakt: |
E-cigarette liquids are complex mixtures of chemicals consisting of humectants, such as propylene glycol (PG) and vegetable glycerin (VG), with nicotine or flavorings added. Published literature emphasizes the toxicity of e-cigarette aerosols with flavorings whereas much less attention has been given to the biologic effects of humectants. The purpose of the current study was to provide a comprehensive view of the acute biologic effects of e-cigarette aerosols on rat bronchoalveolar lavage (BAL) using mass spectrometry-based global proteomics. Sprague-Dawley rats were exposed to e-cigarette aerosol for 3 h/day for three consecutive days. Groups included: PG/VG alone, PG/VG + 2.5% nicotine (N), or PG/VG + N + 3.3% vanillin (V). Right lung lobes were lavaged for BAL and supernatants prepared for proteomics. Extracellular BAL S100A9 concentrations and BAL cell staining for citrullinated histone H3 (citH3) were also performed. From global proteomics, ∼2,100 proteins were identified from rat BAL. The greatest change in number of BAL proteins occurred with PG/VG exposures alone compared with controls with biological pathways enriched for acute phase responses, extracellular trap formation, and coagulation. Extracellular BAL S100A9 concentrations and the number of citH3 + BAL cells also increased significantly in PG/VG and PG/VG + 2.5% N. In contrast to PG/VG or PG/VG + N, the addition of vanillin to PG/VG + N increased BAL neutrophilia and downregulated lipid transport proteins. In summary, global proteomics support e-cigarette aerosol exposures to PG/VG alone as having a significant biologic effect on the lung independent of nicotine or flavoring with increased markers of extracellular trap formation. |
