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Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study
BACKGROUND: Many epidemiological studies have shown that mass concentrations of ambient particulate matter (PM) are associated with adverse health effects in the human population. Since PM is still a very crude measure, this experimental study has explored the role of two distinct size fractions: ul...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513241/ https://www.ncbi.nlm.nih.gov/pubmed/16700918 http://dx.doi.org/10.1186/1743-8977-3-7 |
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author | Kooter, Ingeborg M Boere, A John F Fokkens, Paul HB Leseman, Daan LAC Dormans, Jan AMA Cassee, Flemming R |
author_facet | Kooter, Ingeborg M Boere, A John F Fokkens, Paul HB Leseman, Daan LAC Dormans, Jan AMA Cassee, Flemming R |
author_sort | Kooter, Ingeborg M |
collection | PubMed |
description | BACKGROUND: Many epidemiological studies have shown that mass concentrations of ambient particulate matter (PM) are associated with adverse health effects in the human population. Since PM is still a very crude measure, this experimental study has explored the role of two distinct size fractions: ultrafine (<0.15 μm) and fine (0.15- 2.5 μm) PM. In a series of 2-day inhalation studies, spontaneously hypersensitive (SH) rats were exposed to fine, concentrated, ambient PM (fCAP) at a city background location or a combination of ultrafine and fine (u+fCAP) PM at a location dominated by traffic. We examined the effect on inflammation and both pathological and haematological indicators as markers of pulmonary and cardiovascular injury. Exposure concentrations ranged from 399 μg/m(3 )to 3613 μg/m(3 )for fCAP and from 269μg/m(3 )to 556 μg/m(3 )for u+fCAP. RESULTS: Ammonium, nitrate, and sulphate ions accounted for 56 ± 16% of the total fCAP mass concentrations, but only 17 ± 6% of the u+fCAP mass concentrations. Unambiguous particle uptake in alveolar macrophages was only seen after u+fCAP exposures. Neither fCAP nor u+fCAP induced significant changes of cytotoxicity or inflammation in the lung. However, markers of oxidative stress (heme oxygenase-1 and malondialdehyde) were affected by both fCAP and u+fCAP exposure, although not always significantly. Additional analysis revealed heme oxygenase-1 (HO-1) levels that followed a nonmonotonic function with an optimum at around 600 μg/m(3 )for fCAP. As a systemic response, exposure to u+fCAP and fCAP resulted in significant decreases of the white blood cell concentrations. CONCLUSION: Minor pulmonary and systemic effects are observed after both fine and ultrafine + fine PM exposure. These effects do not linearly correlate with the CAP mass. A greater component of traffic CAP and/or a larger proportion ultrafine PM does not strengthen the absolute effects. |
format | Text |
id | pubmed-1513241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15132412006-07-20 Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study Kooter, Ingeborg M Boere, A John F Fokkens, Paul HB Leseman, Daan LAC Dormans, Jan AMA Cassee, Flemming R Part Fibre Toxicol Research BACKGROUND: Many epidemiological studies have shown that mass concentrations of ambient particulate matter (PM) are associated with adverse health effects in the human population. Since PM is still a very crude measure, this experimental study has explored the role of two distinct size fractions: ultrafine (<0.15 μm) and fine (0.15- 2.5 μm) PM. In a series of 2-day inhalation studies, spontaneously hypersensitive (SH) rats were exposed to fine, concentrated, ambient PM (fCAP) at a city background location or a combination of ultrafine and fine (u+fCAP) PM at a location dominated by traffic. We examined the effect on inflammation and both pathological and haematological indicators as markers of pulmonary and cardiovascular injury. Exposure concentrations ranged from 399 μg/m(3 )to 3613 μg/m(3 )for fCAP and from 269μg/m(3 )to 556 μg/m(3 )for u+fCAP. RESULTS: Ammonium, nitrate, and sulphate ions accounted for 56 ± 16% of the total fCAP mass concentrations, but only 17 ± 6% of the u+fCAP mass concentrations. Unambiguous particle uptake in alveolar macrophages was only seen after u+fCAP exposures. Neither fCAP nor u+fCAP induced significant changes of cytotoxicity or inflammation in the lung. However, markers of oxidative stress (heme oxygenase-1 and malondialdehyde) were affected by both fCAP and u+fCAP exposure, although not always significantly. Additional analysis revealed heme oxygenase-1 (HO-1) levels that followed a nonmonotonic function with an optimum at around 600 μg/m(3 )for fCAP. As a systemic response, exposure to u+fCAP and fCAP resulted in significant decreases of the white blood cell concentrations. CONCLUSION: Minor pulmonary and systemic effects are observed after both fine and ultrafine + fine PM exposure. These effects do not linearly correlate with the CAP mass. A greater component of traffic CAP and/or a larger proportion ultrafine PM does not strengthen the absolute effects. BioMed Central 2006-05-15 /pmc/articles/PMC1513241/ /pubmed/16700918 http://dx.doi.org/10.1186/1743-8977-3-7 Text en Copyright © 2006 Kooter 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 cited. |
spellingShingle | Research Kooter, Ingeborg M Boere, A John F Fokkens, Paul HB Leseman, Daan LAC Dormans, Jan AMA Cassee, Flemming R Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title | Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title_full | Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title_fullStr | Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title_full_unstemmed | Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title_short | Response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
title_sort | response of spontaneously hypertensive rats to inhalation of fine and ultrafine particles from traffic: experimental controlled study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513241/ https://www.ncbi.nlm.nih.gov/pubmed/16700918 http://dx.doi.org/10.1186/1743-8977-3-7 |
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