Comparative cardiopulmonary toxicity of exhausts from soy-based biofuels and diesel in healthy and hypertensive rats

Increased use of renewable energy sources raise concerns about health effects of new emissions. We analyzed relative cardiopulmonary health effects of exhausts from (1) 100% soy biofuel (B100), (2) 20% soy biofuel + 80% low sulfur petroleum diesel (B20), and (3) 100% petroleum diesel (B0) in rats. Normotensive Wistar–Kyoto (WKY) and spontaneously hypertensive rats were exposed to these three exhausts at 0, 50, 150 and 500 μg/m3, 4 h/day for 2 days or 4 weeks (5 days/week). In addition, WKY rats were exposed for 1 day and responses were analyzed 0 h, 1 day or 4 days later for time-course assessment. Hematological parameters, in vitro platelet aggregation, bronchoalveolar lavage fluid (BALF) markers of pulmonary injury and inflammation, ex vivo aortic ring constriction, heart and aorta mRNA markers of vasoconstriction, thrombosis and atherogenesis were analyzed. The presence of pigmented macrophages in the lung alveoli was clearly evident with all three exhausts without apparent pathology. Overall, exposure to all three exhausts produced only modest effects in most endpoints analyzed in both strains. BALF γ-glutamyl transferase (GGT) activity was the most consistent marker and was increased in both strains, primarily with B0 (B0 > B100 > B20). This increase was associated with only modest increases in BALF neutrophils. Small and very acute increases occurred in aorta mRNA markers of vasoconstriction and thrombosis with B100 but not B0 in WKY rats. Our comparative evaluations show modest cardiovascular and pulmonary effects at low concentrations of all exhausts: B0 causing more pulmonary injury and B100 more acute vascular effects. BALF GGT activity could serve as a sensitive biomarker of inhaled pollutants.

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PID https://www.doi.org/10.3109/08958378.2015.1060279
PID https://www.doi.org/10.6084/m9.figshare.1589745
PID pmc:PMC4768834
PID pmid:26514782
PID https://www.doi.org/10.6084/m9.figshare.1589745.v1
PID https://www.doi.org/10.17615/f7hw-r445
URL http://dx.doi.org/10.3109/08958378.2015.1060279
URL https://core.ac.uk/display/150156547
URL https://europepmc.org/articles/PMC4768834/
URL https://www.tandfonline.com/doi/pdf/10.3109/08958378.2015.1060279
URL https://www.cabdirect.org/abstracts/20153434353.html
URL http://dx.doi.org/10.6084/m9.figshare.1589745
URL http://dx.doi.org/10.6084/m9.figshare.1589745.v1
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768834/
URL http://europepmc.org/articles/PMC4768834
URL http://www.tandfonline.com/doi/full/10.3109/08958378.2015.1060279
URL https://www.tandfonline.com/doi/full/10.3109/08958378.2015.1060279
URL https://academic.microsoft.com/#/detail/2212765738
URL https://www.cabdirect.org/cabdirect/abstract/20153434353
URL http://europepmc.org/articles/pmc4768834?pdf=render
URL http://dx.doi.org/10.17615/f7hw-r445
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Access Right Open Access
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Author Virginia Bass, 0000-0001-6219-2448
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Collected From PubMed Central; ORCID; UnpayWall; Datacite; figshare; Crossref; Microsoft Academic Graph
Hosted By Europe PubMed Central; UNC Dataverse; Inhalation Toxicology; figshare
Journal Inhalation Toxicology, 27, null
Publication Date 2015-01-01
Publisher Informa UK Limited
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Resource Type Other literature type; Article
keyword keywords.Health, Toxicology and Mutagenesis
keyword FOS: Biological sciences
keyword FOS: Earth and related environmental sciences
system:type publication
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::7e5542de902cb9fe358d9cde7b146f55
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Last Updated 26 December 2020, 19:46 (CET)
Created 26 December 2020, 19:46 (CET)