Comparative Toxicity of Size-Fractionated Airborne Particulate Matter Collected at Different Distances from an Urban Highway

• Published in: Environmental health perspectives 2009-11, Vol.117 (11), p.1682-1689
• Main Authors: Cho, Seung-Hyun, Tong, Haiyan, McGee, John K., Baldauf, Richard W., Krantz, Q. Todd, Gilmour, M. Ian
• Format: Article
• Language: English
• Subjects: Acute Lung Injury - chemically induced; Acute Lung Injury - physiopathology; Aerosols; Air Pollutants - chemistry; Air Pollutants - toxicity; Air pollution; Animals; Biomarkers - metabolism; Carbon; Chemical hazards; Cytokines; Endotoxins - chemistry; Endotoxins - toxicity; Environmental agencies; Female; Health aspects; Heart diseases; Inflammation - chemically induced; Inflammation - physiopathology; Inhalation Exposure - adverse effects; Lung diseases; Metals - chemistry; Metals - toxicity; Mice; Myocardial Reperfusion Injury - chemically induced; Myocardial Reperfusion Injury - physiopathology; North Carolina; Particle Size; Particulate Matter - chemistry; Particulate Matter - toxicity; Perceptual localization; Pollutant emissions; Risk factors; Roads; Time Factors; Toxic emissions; Vehicle Emissions - toxicity
• ISSN: 0091-6765; 1552-9924
• DOI: 10.1289/ehp.0900730

Background: Epidemiologic studies have reported an association between proximity to highway traffic and increased cardiopulmonary illnesses. Objectives: We investigated the effect of size-fractionated particuiate matter (PM), obtained at different distances from a highway, on acute cardiopulmonary toxicity in mice. Methods: We collected PM for 2 weeks in July-August 2006 using a three-stage (ultrafine, < 0.1 μm; fine, 0.1-2.5 μm; coarse, 2.5-10 μm) high-volume impactor at distances of 20 m [near road (NR)] and 275 m [far road (FR)] from an interstate highway in Raleigh, North Carolina. Samples were extracted in methanol, dried, diluted in saline, and then analyzed for chemical constituents. Female CD-1 mice received either 25 or 100 μg of each size fraction via oropharyngeal aspiration. At 4 and 18 hr postexposure, mice were assessed for pulmonary responsiveness to inhaled methacholine, biomarkers of lung injury and inflammation; ex vivo cardiac pathophysiology was assessed at 18 hr only. Results: Overall chemical composition between NR and FR PM was similar, although NR samples comprised larger amounts of PM, endotoxin, and certain metals than did the FR samples. Kach PM size fraction showed differences in ratios of major chemical classes. Both NR and FR coarse PM produced significant pulmonary inflammation irrespective of distance, whereas both NR and FR ultrafine PM induced cardiac ischemia-reperfusion injury. Conclusions: On a comparative mass basis, the coarse and ultrafine PM affected the lung and heart, respectively. We observed no significant differences in the overall toxicity end points and chemical makeup between the NR and FR PM. The results suggest that PM of different size-specific chemistry might be associated with different toxicologic mechanisms in cardiac and pulmonary tissues.