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Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats

Epidemiological studies link traffic-related air pollution (TRAP) to increased risk for various neurodevelopmental disorders (NDDs); however, there are limited preclinical data demonstrating a causal relationship between TRAP and adverse neurodevelopmental outcomes. Moreover, much of the preclinical...

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Autores principales: Patten, Kelley T., González, Eduardo A., Valenzuela, Anthony, Berg, Elizabeth, Wallis, Christopher, Garbow, Joel R., Silverman, Jill L., Bein, Keith J., Wexler, Anthony S., Lein, Pamela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264203/
https://www.ncbi.nlm.nih.gov/pubmed/32483143
http://dx.doi.org/10.1038/s41398-020-0845-3
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author Patten, Kelley T.
González, Eduardo A.
Valenzuela, Anthony
Berg, Elizabeth
Wallis, Christopher
Garbow, Joel R.
Silverman, Jill L.
Bein, Keith J.
Wexler, Anthony S.
Lein, Pamela J.
author_facet Patten, Kelley T.
González, Eduardo A.
Valenzuela, Anthony
Berg, Elizabeth
Wallis, Christopher
Garbow, Joel R.
Silverman, Jill L.
Bein, Keith J.
Wexler, Anthony S.
Lein, Pamela J.
author_sort Patten, Kelley T.
collection PubMed
description Epidemiological studies link traffic-related air pollution (TRAP) to increased risk for various neurodevelopmental disorders (NDDs); however, there are limited preclinical data demonstrating a causal relationship between TRAP and adverse neurodevelopmental outcomes. Moreover, much of the preclinical literature reports effects of concentrated ambient particles or diesel exhaust that do not recapitulate the complexity of real-world TRAP exposures. To assess the developmental neurotoxicity of more realistic TRAP exposures, we exposed male and female rats during gestation and early postnatal development to TRAP drawn directly from a traffic tunnel in Northern California and delivered to animals in real-time. We compared NDD-relevant neuropathological outcomes at postnatal days 51–55 in TRAP-exposed animals versus control subjects exposed to filtered air. As indicated by immunohistochemical analyses, TRAP significantly increased microglial infiltration in the CA1 hippocampus, but decreased astrogliosis in the dentate gyrus. TRAP exposure had no persistent effect on pro-inflammatory cytokine levels in the male or female brain, but did significantly elevate the anti-inflammatory cytokine IL-10 in females. In male rats, TRAP significantly increased hippocampal neurogenesis, while in females, TRAP increased granule cell layer width. TRAP had no effect on apoptosis in either sex. Magnetic resonance imaging revealed that TRAP-exposed females, but not males, also exhibited decreased lateral ventricular volume, which was correlated with increased granule cell layer width in the hippocampus in females. Collectively, these data indicate that exposure to real-world levels of TRAP during gestation and early postnatal development modulate neurodevelopment, corroborating epidemiological evidence of an association between TRAP exposure and increased risk of NDDs.
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spelling pubmed-72642032020-06-10 Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats Patten, Kelley T. González, Eduardo A. Valenzuela, Anthony Berg, Elizabeth Wallis, Christopher Garbow, Joel R. Silverman, Jill L. Bein, Keith J. Wexler, Anthony S. Lein, Pamela J. Transl Psychiatry Article Epidemiological studies link traffic-related air pollution (TRAP) to increased risk for various neurodevelopmental disorders (NDDs); however, there are limited preclinical data demonstrating a causal relationship between TRAP and adverse neurodevelopmental outcomes. Moreover, much of the preclinical literature reports effects of concentrated ambient particles or diesel exhaust that do not recapitulate the complexity of real-world TRAP exposures. To assess the developmental neurotoxicity of more realistic TRAP exposures, we exposed male and female rats during gestation and early postnatal development to TRAP drawn directly from a traffic tunnel in Northern California and delivered to animals in real-time. We compared NDD-relevant neuropathological outcomes at postnatal days 51–55 in TRAP-exposed animals versus control subjects exposed to filtered air. As indicated by immunohistochemical analyses, TRAP significantly increased microglial infiltration in the CA1 hippocampus, but decreased astrogliosis in the dentate gyrus. TRAP exposure had no persistent effect on pro-inflammatory cytokine levels in the male or female brain, but did significantly elevate the anti-inflammatory cytokine IL-10 in females. In male rats, TRAP significantly increased hippocampal neurogenesis, while in females, TRAP increased granule cell layer width. TRAP had no effect on apoptosis in either sex. Magnetic resonance imaging revealed that TRAP-exposed females, but not males, also exhibited decreased lateral ventricular volume, which was correlated with increased granule cell layer width in the hippocampus in females. Collectively, these data indicate that exposure to real-world levels of TRAP during gestation and early postnatal development modulate neurodevelopment, corroborating epidemiological evidence of an association between TRAP exposure and increased risk of NDDs. Nature Publishing Group UK 2020-05-27 /pmc/articles/PMC7264203/ /pubmed/32483143 http://dx.doi.org/10.1038/s41398-020-0845-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Patten, Kelley T.
González, Eduardo A.
Valenzuela, Anthony
Berg, Elizabeth
Wallis, Christopher
Garbow, Joel R.
Silverman, Jill L.
Bein, Keith J.
Wexler, Anthony S.
Lein, Pamela J.
Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title_full Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title_fullStr Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title_full_unstemmed Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title_short Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats
title_sort effects of early life exposure to traffic-related air pollution on brain development in juvenile sprague-dawley rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264203/
https://www.ncbi.nlm.nih.gov/pubmed/32483143
http://dx.doi.org/10.1038/s41398-020-0845-3
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