| Literature DB >> 25846365 |
Annette Dalrymple1, Patricia Ordoñez2, David Thorne3, Debbie Dillon3, Clive Meredith3.
Abstract
Smoking is a cause of serious diseases, including lung cancer, emphysema, chronic bronchitis and heart disease. DNA damage is thought to be one of the mechanisms by which cigarette smoke (CS) initiates disease in the lung. Indeed, CS induced DNA damage can be measured in vitro and in vivo. The potential of the Comet assay to measure DNA damage in isolated rat lung alveolar type II epithelial cells (AEC II) was explored as a means to include a genotoxicity end-point in rodent sub-chronic inhalation studies. In this study, published AEC II isolation methods were improved to yield viable cells suitable for use in the Comet assay. The improved method reduced the level of basal DNA damage and DNA repair in isolated AEC II. CS induced DNA damage could also be quantified in isolated cells following a single or 5 days CS exposure. In conclusion, the Comet assay has the potential to determine CS or other aerosol induced DNA damage in AEC II isolated from rodents used in sub-chronic inhalation studies.Entities:
Keywords: 3R4F reference cigarette; Alveolar type II cells (AEC II); Cigarette smoke; Comet assay; DNA damage; Genotoxicity endpoint; Rat
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Year: 2015 PMID: 25846365 DOI: 10.1016/j.yrtph.2015.03.013
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271