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Comparative study on gene expression profile in rat lung after repeated exposure to diesel and biodiesel exhausts upstream and downstream of a particle filter
- Source :
- Environmental Pollution, Environmental Pollution, 2020, 266 (Part 2), pp.115264. ⟨10.1016/j.envpol.2020.115264⟩, Environmental Pollution (Elsevier), Environmental Pollution (Elsevier), 2020, 266 (Pt 2), pp.115264. ⟨10.1016/j.envpol.2020.115264⟩
- Publication Year :
- 2020
- Publisher :
- HAL CCSD, 2020.
-
Abstract
- International audience; Biodiesel is considered as a valuable and less toxic alternative to diesel. However, cellular and molecular effects of repeated exposure to biodiesel emissions from a recent engine equipped with a diesel particle filter (DPF) remain to be characterized. To gain insights about this point, the lung transcriptional signatures were analyzed for rats (n = 6 per group) exposed to filtered air, 30% rapeseed biodiesel (B30) blend or reference diesel (RF0), upstream and downstream a DPF, for 3 weeks (3 h/day, 5 days/week). Genomic analysis revealed a modest regulation of gene expression level (lower than a 2-fold) by both fuels and a higher number of genes regulated downstream the DPF than upstream, in response to either RF0 or to B30 exhaust emissions. The presence of DPF was found to notably impact the lung gene signature of rats exposed to B30. The number of genes regulated in common by both fuels was low, which is likely due to differences in concentrations of regulated pollutants in exhausts, notably for compound organic volatiles, polycyclic aromatic hydrocarbons, NO or NOx. Nevertheless, we have identified some pathways that were activated for both exhaust emissions, such as integrin-, IGF-1- and Rac-signaling pathways, likely reflecting the effects of gas phase products. By contrast, some canonical pathways relative to "oxidative phosphorylation" and "mitochondrial dysfunction" appear as specific to B30 exhaust emission; the repression of transcripts of mitochondrial respiratory chain in lung of rats exposed to B30 downstream of DPF supports the perturbation of mitochondria function. This study done with a recent diesel engine (compliant with the European IV emission standard) and commercially-available fuels reveals that the diesel blend composition and the presence of an after treatment system may modify lung gene signature of rats repeatedly exposed to exhaust emissions, however in a rather modest manner.
- Subjects :
- Diesel exhaust
010504 meteorology & atmospheric sciences
Health, Toxicology and Mutagenesis
[SDV]Life Sciences [q-bio]
010501 environmental sciences
Toxicology
Diesel engine
01 natural sciences
complex mixtures
Diesel fuel
Particle filter
Animals
Lung
NOx
0105 earth and related environmental sciences
Vehicle Emissions
Regulation of gene expression
Biodiesel
Air Pollutants
Diesel particulate filter
Chemistry
General Medicine
Pollution
3. Good health
Cell biology
Rats
[SDV] Life Sciences [q-bio]
Mitochondrial respiratory chain
13. Climate action
Biofuels
Particulate Matter
Transcriptome analysis
Transcriptome
Gasoline
Subjects
Details
- Language :
- English
- ISSN :
- 02697491 and 18736424
- Database :
- OpenAIRE
- Journal :
- Environmental Pollution, Environmental Pollution, 2020, 266 (Part 2), pp.115264. ⟨10.1016/j.envpol.2020.115264⟩, Environmental Pollution (Elsevier), Environmental Pollution (Elsevier), 2020, 266 (Pt 2), pp.115264. ⟨10.1016/j.envpol.2020.115264⟩
- Accession number :
- edsair.doi.dedup.....9c81df40ce8e9a2e5a948a53b35f17b1
- Full Text :
- https://doi.org/10.1016/j.envpol.2020.115264⟩