| Literature DB >> 30685595 |
Pål Magnusson1, Katarzyna Dziendzikowska2, Michał Oczkowski2, Johan Øvrevik1, Dag M Eide1, Gunnar Brunborg1, Kristine B Gutzkow1, Christine Instanes1, Malgorzata Gajewska3, Jacek Wilczak3, Rafał Sapierzynski3, Dariusz Kamola3, Tomasz Królikowski2, Marcin Kruszewski4, Anna Lankoff5, Remigiusz Mruk6, Nur Duale1, Joanna Gromadzka-Ostrowska2, Oddvar Myhre7.
Abstract
Increased use of 1st and 2nd generation biofuels raises concerns about health effects of new emissions. We analyzed cellular and molecular lung effects in Fisher 344 rats exposed to diesel engine exhaust emissions (DEE) from a Euro 5-classified diesel engine running on B7: petrodiesel fuel containing 7% fatty acid methyl esters (FAME), or SHB20 (synthetic hydrocarbon biofuel): petrodiesel fuel containing 7% FAME and 13% hydrogenated vegetable oil. The Fisher 344 rats were exposed for 7 consecutive days (6 h/day) or 28 days (6 h/day, 5 days/week), both with and without diesel particle filter (DPF) treatment of the exhaust in whole body exposure chambers (n = 7/treatment). Histological analysis and analysis of cytokines and immune cell numbers in bronchoalveolar lavage fluid (BALF) did not reveal adverse pulmonary effects after exposure to DEE from B7 or SHB20 fuel. Significantly different gene expression levels for B7 compared to SHB20 indicate disturbed redox signaling (Cat, Hmox1), beta-adrenergic signaling (Adrb2) and xenobiotic metabolism (Cyp1a1). Exhaust filtration induced higher expression of redox genes (Cat, Gpx2) and the chemokine gene Cxcl7 compared to non-filtered exhaust. Exposure time (7 versus 28 days) also resulted in different patterns of lung gene expression. No genotoxic effects in the lungs were observed. Overall, exposure to B7 or SHB20 emissions suggests only minor effects in the lungs.Entities:
Keywords: Air pollution; Particle matter (PM); Petroleum diesel; Polycyclic aromatic hydrocarbons (PAHs); Pulmonary toxicity
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Year: 2019 PMID: 30685595 DOI: 10.1016/j.etap.2019.01.005
Source DB: PubMed Journal: Environ Toxicol Pharmacol ISSN: 1382-6689 Impact factor: 4.860