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Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice

BACKGROUND: Results from epidemiological studies indicate that particulate air pollution constitutes a hazard for human health. Recent studies suggest that diesel exhaust possesses endocrine activity and therefore may affect reproductive outcome. This study in mice aimed to investigate whether expos...

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Autores principales: Hougaard, Karin S, Jensen, Keld A, Nordly, Pernille, Taxvig, Camilla, Vogel, Ulla, Saber, Anne T, Wallin, Håkan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323399/
https://www.ncbi.nlm.nih.gov/pubmed/18331653
http://dx.doi.org/10.1186/1743-8977-5-3
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author Hougaard, Karin S
Jensen, Keld A
Nordly, Pernille
Taxvig, Camilla
Vogel, Ulla
Saber, Anne T
Wallin, Håkan
author_facet Hougaard, Karin S
Jensen, Keld A
Nordly, Pernille
Taxvig, Camilla
Vogel, Ulla
Saber, Anne T
Wallin, Håkan
author_sort Hougaard, Karin S
collection PubMed
description BACKGROUND: Results from epidemiological studies indicate that particulate air pollution constitutes a hazard for human health. Recent studies suggest that diesel exhaust possesses endocrine activity and therefore may affect reproductive outcome. This study in mice aimed to investigate whether exposure to diesel exhaust particles (DEP; NIST 2975) would affect gestation, postnatal development, activity, learning and memory, and biomarkers of transplacental toxicity. Pregnant mice (C57BL/6; BomTac) were exposed to 19 mg/m(3 )DEP (~1·10(6 )particles/cm(3); mass median diameter ≅ 240 nm) on gestational days 9–19, for 1 h/day. RESULTS: Gestational parameters were similar in control and diesel groups. Shortly after birth, body weights of DEP offspring were slightly lower than in controls. This difference increased during lactation, so by weaning the DEP exposed offspring weighed significantly less than the control progeny. Only slight effects of exposure were observed on cognitive function in female DEP offspring and on biomarkers of exposure to particles or genotoxic substances. CONCLUSION: In utero exposure to DEP decreased weight gain during lactation. Cognitive function and levels of biomarkers of exposure to particles or to genotoxic substances were generally similar in exposed and control offspring. The particle size and chemical composition of the DEP and differences in exposure methods (fresh, whole exhaust versus aged, resuspended DEP) may play a significant role on the biological effects observed in this compared to other studies.
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spelling pubmed-23233992008-04-19 Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice Hougaard, Karin S Jensen, Keld A Nordly, Pernille Taxvig, Camilla Vogel, Ulla Saber, Anne T Wallin, Håkan Part Fibre Toxicol Research BACKGROUND: Results from epidemiological studies indicate that particulate air pollution constitutes a hazard for human health. Recent studies suggest that diesel exhaust possesses endocrine activity and therefore may affect reproductive outcome. This study in mice aimed to investigate whether exposure to diesel exhaust particles (DEP; NIST 2975) would affect gestation, postnatal development, activity, learning and memory, and biomarkers of transplacental toxicity. Pregnant mice (C57BL/6; BomTac) were exposed to 19 mg/m(3 )DEP (~1·10(6 )particles/cm(3); mass median diameter ≅ 240 nm) on gestational days 9–19, for 1 h/day. RESULTS: Gestational parameters were similar in control and diesel groups. Shortly after birth, body weights of DEP offspring were slightly lower than in controls. This difference increased during lactation, so by weaning the DEP exposed offspring weighed significantly less than the control progeny. Only slight effects of exposure were observed on cognitive function in female DEP offspring and on biomarkers of exposure to particles or genotoxic substances. CONCLUSION: In utero exposure to DEP decreased weight gain during lactation. Cognitive function and levels of biomarkers of exposure to particles or to genotoxic substances were generally similar in exposed and control offspring. The particle size and chemical composition of the DEP and differences in exposure methods (fresh, whole exhaust versus aged, resuspended DEP) may play a significant role on the biological effects observed in this compared to other studies. BioMed Central 2008-03-11 /pmc/articles/PMC2323399/ /pubmed/18331653 http://dx.doi.org/10.1186/1743-8977-5-3 Text en Copyright © 2008 Hougaard 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
Hougaard, Karin S
Jensen, Keld A
Nordly, Pernille
Taxvig, Camilla
Vogel, Ulla
Saber, Anne T
Wallin, Håkan
Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title_full Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title_fullStr Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title_full_unstemmed Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title_short Effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
title_sort effects of prenatal exposure to diesel exhaust particles on postnatal development, behavior, genotoxicity and inflammation in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323399/
https://www.ncbi.nlm.nih.gov/pubmed/18331653
http://dx.doi.org/10.1186/1743-8977-5-3
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