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

被引:21
作者
Bass, Virginia L. [1 ]
Schladweiler, Mette C. [2 ]
Nyska, Abraham [3 ]
Thomas, Ronald F. [2 ]
Miller, Desinia B. [4 ]
Krantz, Todd [2 ]
King, Charly [2 ]
Gilmour, M. Ian [2 ]
Ledbetter, Allen D. [2 ]
Richards, Judy E. [2 ]
Kodavanti, Urmila P. [2 ]
机构
[1] Univ N Carolina, Sch Publ Hlth, Environm Sci & Engn, Chapel Hill, NC USA
[2] US EPA, Natl Hlth & Environm Effects Res Lab, Environm Publ Hlth Div, Res Triangle Pk, NC 27711 USA
[3] Tel Aviv Univ, Sackler Sch Med, Consultant Toxicol Pathol, Timrat, Israel
[4] Univ N Carolina, Curriculum Toxicol, Chapel Hill, NC USA
关键词
Biodiesel; biomarkers; hypertensive rats; pulmonary toxicity; toxicity; LONG-TERM EXPOSURE; BROWN-NORWAY RATS; PARTICULATE MATTER; OXIDATIVE STRESS; CARDIOVASCULAR-DISEASE; INHALATION; BIODIESEL; PULMONARY; PARTICLES; FUEL;
D O I
10.3109/08958378.2015.1060279
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 500g/m(3), 4h/day for 2 days or 4 weeks (5 days/week). In addition, WKY rats were exposed for 1 day and responses were analyzed 0h, 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 -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.
引用
收藏
页码:545 / 556
页数:12
相关论文
共 36 条
[1]   Diesel exhaust particulate matter induces multinucleate cells and zinc transporter-dependent apoptosis in human airway cells [J].
Ackland, Margaret Leigh ;
Zou, Linda ;
Freestone, David ;
van de Waasenburg, Simone ;
Michalczyk, Agnes A. .
IMMUNOLOGY AND CELL BIOLOGY, 2007, 85 (08) :617-622
[2]   Long-term exposure to traffic-related PM10 and decreased heart rate variability: Is the association restricted to subjects taking ACE inhibitors? [J].
Adam, Martin ;
Dietrich, Denise Felber ;
Schaffner, Emmanuel ;
Carballo, David ;
Barthelemy, Jean-Claude ;
Gaspoz, Jean-Michel ;
Tsai, Ming-Yi ;
Rapp, Regula ;
Phuleria, Harish Chandra ;
Schindler, Christian ;
Schwartz, Joel ;
Kuenzli, Nino ;
Probst-Hensch, Nicole M. .
ENVIRONMENT INTERNATIONAL, 2012, 48 :9-16
[3]   Ozone induces glucose intolerance and systemic metabolic effects in young and aged brown Norway rats [J].
Bass, V. ;
Gordon, C. J. ;
Jarema, K. A. ;
MacPhail, R. C. ;
Cascio, W. E. ;
Phillips, P. M. ;
Ledbetter, A. D. ;
Schladweiler, M. C. ;
Andrews, D. ;
Miller, D. ;
Doerfler, D. L. ;
Kodavanti, U. P. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 273 (03) :551-560
[4]   Acute Cardiovascular and Inflammatory Toxicity Induced by Inhalation of Diesel and Biodiesel Exhaust Particles [J].
Brito, Jose Mara ;
Belotti, Luciano ;
Toledo, Alessandra C. ;
Antonangelo, Leila ;
Silva, Flavio S. ;
Alvim, Debora S. ;
Andre, Paulo A. ;
Saldiva, Paulo H. N. ;
Rivero, Dolores H. R. F. .
TOXICOLOGICAL SCIENCES, 2010, 116 (01) :67-78
[5]   Strong mutagenic effects of diesel engine emissions using vegetable oil as fuel [J].
Buenger, Juergen ;
Krahl, Juergen ;
Munack, Axel ;
Ruschel, Yvonne ;
Schroeder, Olaf ;
Emmert, Birgit ;
West, Goetz ;
Mueller, Michael ;
Hallier, Ernst ;
Bruening, Thomas .
ARCHIVES OF TOXICOLOGY, 2007, 81 (08) :599-603
[6]   Mutagenicity of diesel exhaust particles from two fossil and two plant oil fuels [J].
Bünger, J ;
Müller, MM ;
Krahl, J ;
Baum, K ;
Weigel, A ;
Hallier, E ;
Schulz, TG .
MUTAGENESIS, 2000, 15 (05) :391-397
[7]   Mutagenic and cytotoxic effects of exhaust particulate matter of biodiesel compared to fossil diesel fuel [J].
Bünger, J ;
Krahl, J ;
Franke, HU ;
Munack, A ;
Hallier, E .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1998, 415 (1-2) :13-23
[8]  
Buzzard N. A., 2009, ENV HLTH, V8, P1
[9]  
Bye A, 2008, INHAL TOXICOL, V20, P635, DOI [10.1080/08958370701883821, 10.1080/08958370701883821 ]
[10]   Blood Pressure Response to Controlled Diesel Exhaust Exposure in Human Subjects [J].
Cosselman, Kristen E. ;
Krishnan, Ranjini M. ;
Oron, Assaf P. ;
Jansen, Karen ;
Peretz, Alon ;
Sullivan, Jeffrey H. ;
Larson, Timothy V. ;
Kaufman, Joel D. .
HYPERTENSION, 2012, 59 (05) :943-+