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Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations

Coal tar (CT) is a thick black liquid produced as a by‐product of coal carbonization to produce coke or manufactured gas. It is comprised a complex mixture of polycyclic aromatic compounds, including a wide range of polycyclic aromatic hydrocarbons (PAHs), many of which are genotoxic and carcinogeni...

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Autores principales: Long, Alexandra S., Watson, Margaret, Arlt, Volker M., White, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979669/
https://www.ncbi.nlm.nih.gov/pubmed/27473530
http://dx.doi.org/10.1002/em.22032
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author Long, Alexandra S.
Watson, Margaret
Arlt, Volker M.
White, Paul A.
author_facet Long, Alexandra S.
Watson, Margaret
Arlt, Volker M.
White, Paul A.
author_sort Long, Alexandra S.
collection PubMed
description Coal tar (CT) is a thick black liquid produced as a by‐product of coal carbonization to produce coke or manufactured gas. It is comprised a complex mixture of polycyclic aromatic compounds, including a wide range of polycyclic aromatic hydrocarbons (PAHs), many of which are genotoxic and carcinogenic. CT is used in some pavement sealants (also known as sealcoat), which are applied to pavement in order to seal and beautify the surface. Human exposure is known to occur not only during application, but also as a result of the weathering process, as elevated levels of PAHs have been found in settled house dust in residences adjacent to CT‐sealed surfaces. In this study we examined the genotoxicity of an extract of a commercially available CT‐based sealcoat in the transgenic Muta™Mouse model. Mice were orally exposed to 3 doses of sealcoat extract daily for 28 days. We evaluated genotoxicity by examining: (1) stable DNA adducts and (2) lacZ mutations in bone marrow, liver, lung, small intestine, and glandular stomach, as well as (3) micronucleated red blood cells. Significant increases were seen for each endpoint and in all tissues. The potency of the response differed across tissues, with the highest frequency of adducts occurring in liver and lung, and the highest frequency of mutations occurring in small intestine. The results of this study are the first demonstration of mammalian genotoxicity following exposure to CT‐containing pavement sealcoat. This work provides in vivo evidence to support the contention that there may be adverse health effects in mammals, and potentially in humans, from exposure to coal tar. Environ. Mol. Mutagen. 57:535–545, 2016. © 2016 Her Majesty the Queen in Right of Canada
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spelling pubmed-49796692016-08-23 Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations Long, Alexandra S. Watson, Margaret Arlt, Volker M. White, Paul A. Environ Mol Mutagen Research Articles Coal tar (CT) is a thick black liquid produced as a by‐product of coal carbonization to produce coke or manufactured gas. It is comprised a complex mixture of polycyclic aromatic compounds, including a wide range of polycyclic aromatic hydrocarbons (PAHs), many of which are genotoxic and carcinogenic. CT is used in some pavement sealants (also known as sealcoat), which are applied to pavement in order to seal and beautify the surface. Human exposure is known to occur not only during application, but also as a result of the weathering process, as elevated levels of PAHs have been found in settled house dust in residences adjacent to CT‐sealed surfaces. In this study we examined the genotoxicity of an extract of a commercially available CT‐based sealcoat in the transgenic Muta™Mouse model. Mice were orally exposed to 3 doses of sealcoat extract daily for 28 days. We evaluated genotoxicity by examining: (1) stable DNA adducts and (2) lacZ mutations in bone marrow, liver, lung, small intestine, and glandular stomach, as well as (3) micronucleated red blood cells. Significant increases were seen for each endpoint and in all tissues. The potency of the response differed across tissues, with the highest frequency of adducts occurring in liver and lung, and the highest frequency of mutations occurring in small intestine. The results of this study are the first demonstration of mammalian genotoxicity following exposure to CT‐containing pavement sealcoat. This work provides in vivo evidence to support the contention that there may be adverse health effects in mammals, and potentially in humans, from exposure to coal tar. Environ. Mol. Mutagen. 57:535–545, 2016. © 2016 Her Majesty the Queen in Right of Canada John Wiley and Sons Inc. 2016-07-30 2016-08 /pmc/articles/PMC4979669/ /pubmed/27473530 http://dx.doi.org/10.1002/em.22032 Text en © 2016 Reproduced with the permission of the Government of Canada This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Long, Alexandra S.
Watson, Margaret
Arlt, Volker M.
White, Paul A.
Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title_full Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title_fullStr Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title_full_unstemmed Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title_short Oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
title_sort oral exposure to commercially available coal tar‐based pavement sealcoat induces murine genetic damage and mutations
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979669/
https://www.ncbi.nlm.nih.gov/pubmed/27473530
http://dx.doi.org/10.1002/em.22032
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