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Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices

BACKGROUND: Emissions from a large peat fire in North Carolina in 2008 were associated with increased hospital admissions for asthma and the rate of heart failure in the exposed population. Peat fires often produce larger amounts of smoke and last longer than forest fires, however few studies have r...

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Autores principales: Kim, Yong Ho, Tong, Haiyan, Daniels, Mary, Boykin, Elizabeth, Krantz, Q Todd, McGee, John, Hays, Michael, Kovalcik, Kasey, Dye, Janice A, Gilmour, M Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072480/
https://www.ncbi.nlm.nih.gov/pubmed/24934158
http://dx.doi.org/10.1186/1743-8977-11-29
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author Kim, Yong Ho
Tong, Haiyan
Daniels, Mary
Boykin, Elizabeth
Krantz, Q Todd
McGee, John
Hays, Michael
Kovalcik, Kasey
Dye, Janice A
Gilmour, M Ian
author_facet Kim, Yong Ho
Tong, Haiyan
Daniels, Mary
Boykin, Elizabeth
Krantz, Q Todd
McGee, John
Hays, Michael
Kovalcik, Kasey
Dye, Janice A
Gilmour, M Ian
author_sort Kim, Yong Ho
collection PubMed
description BACKGROUND: Emissions from a large peat fire in North Carolina in 2008 were associated with increased hospital admissions for asthma and the rate of heart failure in the exposed population. Peat fires often produce larger amounts of smoke and last longer than forest fires, however few studies have reported on their toxicity. Moreover, reliable alternatives to traditional animal toxicity testing are needed to reduce the number of animals required for hazard identification and risk assessments. METHODS: Size-fractionated particulate matter (PM; ultrafine, fine, and coarse) were obtained from the peat fire while smoldering (ENCF-1) or when nearly extinguished (ENCF-4). Extracted samples were analyzed for chemical constituents and endotoxin content. Female CD-1 mice were exposed via oropharyngeal aspiration to 100 μg/mouse, and assessed for relative changes in lung and systemic markers of injury and inflammation. At 24 h post-exposure, hearts were removed for ex vivo functional assessments and ischemic challenge. Lastly, 8 mm diameter lung slices from CD-1 mice were exposed (11 μg) ± co-treatment of PM with polymyxin B (PMB), an endotoxin-binding compound. RESULTS: On an equi-mass basis, coarse ENCF-1 PM had the highest endotoxin content and elicited the greatest pro-inflammatory responses in the mice including: increases in bronchoalveolar lavage fluid protein, cytokines (IL-6, TNF-α, and MIP-2), neutrophils and intracellular reactive oxygen species (ROS) production. Exposure to fine or ultrafine particles from either period failed to elicit significant lung or systemic effects. In contrast, mice exposed to ENCF-1 ultrafine PM developed significantly decreased cardiac function and greater post-ischemia-associated myocardial infarction. Finally, similar exposures to mouse lung slices induced comparable patterns of cytokine production; and these responses were significantly attenuated by PMB. CONCLUSIONS: The findings suggest that exposure to coarse PM collected during a peat fire causes greater lung inflammation in association with endotoxin and ROS, whereas the ultrafine PM preferentially affected cardiac responses. In addition, lung tissue slices were shown to be a predictive, alternative assay to assess pro-inflammatory effects of PM of differing size and composition. Importantly, these toxicological findings were consistent with the cardiopulmonary health effects noted in epidemiologic reports from exposed populations.
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spelling pubmed-40724802014-06-27 Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices Kim, Yong Ho Tong, Haiyan Daniels, Mary Boykin, Elizabeth Krantz, Q Todd McGee, John Hays, Michael Kovalcik, Kasey Dye, Janice A Gilmour, M Ian Part Fibre Toxicol Research BACKGROUND: Emissions from a large peat fire in North Carolina in 2008 were associated with increased hospital admissions for asthma and the rate of heart failure in the exposed population. Peat fires often produce larger amounts of smoke and last longer than forest fires, however few studies have reported on their toxicity. Moreover, reliable alternatives to traditional animal toxicity testing are needed to reduce the number of animals required for hazard identification and risk assessments. METHODS: Size-fractionated particulate matter (PM; ultrafine, fine, and coarse) were obtained from the peat fire while smoldering (ENCF-1) or when nearly extinguished (ENCF-4). Extracted samples were analyzed for chemical constituents and endotoxin content. Female CD-1 mice were exposed via oropharyngeal aspiration to 100 μg/mouse, and assessed for relative changes in lung and systemic markers of injury and inflammation. At 24 h post-exposure, hearts were removed for ex vivo functional assessments and ischemic challenge. Lastly, 8 mm diameter lung slices from CD-1 mice were exposed (11 μg) ± co-treatment of PM with polymyxin B (PMB), an endotoxin-binding compound. RESULTS: On an equi-mass basis, coarse ENCF-1 PM had the highest endotoxin content and elicited the greatest pro-inflammatory responses in the mice including: increases in bronchoalveolar lavage fluid protein, cytokines (IL-6, TNF-α, and MIP-2), neutrophils and intracellular reactive oxygen species (ROS) production. Exposure to fine or ultrafine particles from either period failed to elicit significant lung or systemic effects. In contrast, mice exposed to ENCF-1 ultrafine PM developed significantly decreased cardiac function and greater post-ischemia-associated myocardial infarction. Finally, similar exposures to mouse lung slices induced comparable patterns of cytokine production; and these responses were significantly attenuated by PMB. CONCLUSIONS: The findings suggest that exposure to coarse PM collected during a peat fire causes greater lung inflammation in association with endotoxin and ROS, whereas the ultrafine PM preferentially affected cardiac responses. In addition, lung tissue slices were shown to be a predictive, alternative assay to assess pro-inflammatory effects of PM of differing size and composition. Importantly, these toxicological findings were consistent with the cardiopulmonary health effects noted in epidemiologic reports from exposed populations. BioMed Central 2014-06-16 /pmc/articles/PMC4072480/ /pubmed/24934158 http://dx.doi.org/10.1186/1743-8977-11-29 Text en Copyright © 2014 Kim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kim, Yong Ho
Tong, Haiyan
Daniels, Mary
Boykin, Elizabeth
Krantz, Q Todd
McGee, John
Hays, Michael
Kovalcik, Kasey
Dye, Janice A
Gilmour, M Ian
Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title_full Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title_fullStr Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title_full_unstemmed Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title_short Cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
title_sort cardiopulmonary toxicity of peat wildfire particulate matter and the predictive utility of precision cut lung slices
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072480/
https://www.ncbi.nlm.nih.gov/pubmed/24934158
http://dx.doi.org/10.1186/1743-8977-11-29
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