| Literature DB >> 27793746 |
Ee Tsin Wong1, Ulrike Kogel2, Emilija Veljkovic1, Florian Martin2, Yang Xiang2, Stephanie Boue2, Gregory Vuillaume2, Patrice Leroy2, Emmanuel Guedj2, Gregory Rodrigo3, Nikolai V Ivanov2, Julia Hoeng2, Manuel C Peitsch2, Patrick Vanscheeuwijck4.
Abstract
The objective of the study was to characterize the toxicity from sub-chronic inhalation of test atmospheres from the candidate modified risk tobacco product (MRTP), Tobacco Heating System version 2.2 (THS2.2), and to compare it with that of the 3R4F reference cigarette. A 90-day nose-only inhalation study on Sprague-Dawley rats was performed, combining classical and systems toxicology approaches. Reduction in respiratory minute volume, degree of lung inflammation, and histopathological findings in the respiratory tract organs were significantly less pronounced in THS2.2-exposed groups compared with 3R4F-exposed groups. Transcriptomics data obtained from nasal epithelium and lung parenchyma showed concentration-dependent differential gene expression following 3R4F exposure that was less pronounced in the THS2.2-exposed groups. Molecular network analysis showed that inflammatory processes were the most affected by 3R4F, while the extent of THS2.2 impact was much lower. Most other toxicological endpoints evaluated did not show exposure-related effects. Where findings were observed, the effects were similar in 3R4F- and THS2.2-exposed animals. In summary, toxicological changes observed in the respiratory tract organs of THS2.2 aerosol-exposed rats were much less pronounced than in 3R4F-exposed rats while other toxicological endpoints either showed no exposure-related effects or were comparable to what was observed in the 3R4F-exposed rats.Entities:
Keywords: Heat-not-burn; Inhalation systems toxicology; Inhalation toxicology study; Modified risk tobacco product; Pulmonary inflammation
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Year: 2016 PMID: 27793746 DOI: 10.1016/j.yrtph.2016.10.015
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271