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Cardiopulmonary Responses of Intratracheally Instilled Tire Particles and Constituent Metal Components 

Authors: Reddy R. Gottipolu a;  Edward R. Landa b;  Mette C. Schladweiler c;  John K. McGee c;  Allen D. Ledbetter c;  Judy H. Richards c;  Grace J. Wallenborn d; Urmila P. Kodavanti c
Affiliations:   a National Research Council, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina, USA
b U.S. Geological Survey, Reston, Virginia, USA
c National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina, USA
d School of Public Health, University of North Carolina, Chapel Hill, North Carolina, USA
DOI: 10.1080/08958370701858427
Publication Frequency: 4 issues per year
Published in: journal Inhalation Toxicology, Volume 20, Issue 5 March 2008 , pages 473 - 484
Formats available: HTML (English) : PDF (English)
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Abstract

Tire and brake wear particles contain transition metals, and contribute to near-road PM. We hypothesized that acute cardiopulmonary injury from respirable tire particles (TP) will depend on the amount of soluble metals. Respirable fractions of two types of TP (TP1 and TP2) were analyzed for water and acid-leachable metals using ICP-AES. Both TP types contained a variety of transition metals, including zinc (Zn), copper (Cu), aluminum, and iron. Zn and Cu were detected at high levels in water-soluble fractions (TP2 > TP1). Male Wistar Kyoto rats (12-14 wk) were intratracheally instilled, in the first study, with saline, TP1 or TP2 (5 mg/kg), and in the second study, with soluble Zn, Cu (0.5 μ mol/kg), or both. Pulmonary toxicity and cardiac mitochondrial enzymes were analyzed 1 d, 1 wk, or 4 wk later for TP and 4 or 24 h later for metals. Increases in lavage fluid markers of inflammation and injury were observed at d 1 (TP2 > TP1), but these changes reversed by wk 1. No effects on cardiac enzymes were noted with either TP. Exposure of rats to soluble Zn and Cu caused marked pulmonary inflammation and injury but temporal differences were apparent (Cu effects peaked at 4 h and Zn at 24 h). Instillation of Zn, Cu, and Zn+ Cu decreased the activity of cardiac aconitase, isocitrate dehydrogenase, succinate dehydrogenase, cytochrome-c-oxidase and superoxide dismutase suggesting mitochondrial oxidative stress. The observed acute pulmonary toxicity of TP could be due to the presence of water soluble Zn and Cu. At high concentrations these metals may induce cardiac oxidative stress.
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