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Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins

The prevalence of cognitive abnormalities in children has partly been ascribed to environmental chemical exposure. Appropriate animal models and tools for evaluating higher brain function are required to examine this problem. A recently developed behavioral test in which rats learn six unique flavor...

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Autores principales: Kakeyama, Masaki, Endo, Toshihiro, Zhang, Yan, Miyazaki, Wataru, Tohyama, Chiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927058/
https://www.ncbi.nlm.nih.gov/pubmed/24292196
http://dx.doi.org/10.1007/s00204-013-1161-y
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author Kakeyama, Masaki
Endo, Toshihiro
Zhang, Yan
Miyazaki, Wataru
Tohyama, Chiharu
author_facet Kakeyama, Masaki
Endo, Toshihiro
Zhang, Yan
Miyazaki, Wataru
Tohyama, Chiharu
author_sort Kakeyama, Masaki
collection PubMed
description The prevalence of cognitive abnormalities in children has partly been ascribed to environmental chemical exposure. Appropriate animal models and tools for evaluating higher brain function are required to examine this problem. A recently developed behavioral test in which rats learn six unique flavor-location pairs in a test arena was used to evaluate paired-associate learning, a hallmark of the higher cognitive function that is essential to language learning in humans. Pregnant Long-Evans rats were dosed by gavage with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) or 2,3,7,8-tetrabromodibenzo-p-dioxin (TBDD) at a dose of  0, 200, or 800 ng/kg (referred as Control, TCDD-200, TCDD-800, TBDD-200, or TBDD-800, hereafter) on gestational day 15, and the offspring was tested during adulthood. Paired-associate learning was found to be impaired in the TCDD-200 and TBDD-200 groups, but not in either group exposed to 800 ng/kg, the observations of which were ensured by non-cued trials. As for the emotional aspect, during habituation, the TCDD-200 and TBDD-200 groups showed significantly longer latencies to enter the test arena from a start box than the Control, TCDD-800, and TBDD-800 groups, suggesting that the TCDD-200 and TBDD-200 groups manifested anxiety-like behavior. Thus, both the chlorinated dioxin and its brominated congener affected higher brain function to a similar extent in a nearly identical manner. Use of the behavioral test that can evaluate paired-associate learning in rats demonstrated that in utero and lactational exposure to not only TCDD but also TBDD perturbed higher brain function in rat offspring in a nonmonotonic manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-013-1161-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-39270582014-02-21 Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins Kakeyama, Masaki Endo, Toshihiro Zhang, Yan Miyazaki, Wataru Tohyama, Chiharu Arch Toxicol Reproductive Toxicology The prevalence of cognitive abnormalities in children has partly been ascribed to environmental chemical exposure. Appropriate animal models and tools for evaluating higher brain function are required to examine this problem. A recently developed behavioral test in which rats learn six unique flavor-location pairs in a test arena was used to evaluate paired-associate learning, a hallmark of the higher cognitive function that is essential to language learning in humans. Pregnant Long-Evans rats were dosed by gavage with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) or 2,3,7,8-tetrabromodibenzo-p-dioxin (TBDD) at a dose of  0, 200, or 800 ng/kg (referred as Control, TCDD-200, TCDD-800, TBDD-200, or TBDD-800, hereafter) on gestational day 15, and the offspring was tested during adulthood. Paired-associate learning was found to be impaired in the TCDD-200 and TBDD-200 groups, but not in either group exposed to 800 ng/kg, the observations of which were ensured by non-cued trials. As for the emotional aspect, during habituation, the TCDD-200 and TBDD-200 groups showed significantly longer latencies to enter the test arena from a start box than the Control, TCDD-800, and TBDD-800 groups, suggesting that the TCDD-200 and TBDD-200 groups manifested anxiety-like behavior. Thus, both the chlorinated dioxin and its brominated congener affected higher brain function to a similar extent in a nearly identical manner. Use of the behavioral test that can evaluate paired-associate learning in rats demonstrated that in utero and lactational exposure to not only TCDD but also TBDD perturbed higher brain function in rat offspring in a nonmonotonic manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-013-1161-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-11-29 2014 /pmc/articles/PMC3927058/ /pubmed/24292196 http://dx.doi.org/10.1007/s00204-013-1161-y Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Reproductive Toxicology
Kakeyama, Masaki
Endo, Toshihiro
Zhang, Yan
Miyazaki, Wataru
Tohyama, Chiharu
Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title_full Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title_fullStr Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title_full_unstemmed Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title_short Disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
title_sort disruption of paired-associate learning in rat offspring perinatally exposed to dioxins
topic Reproductive Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927058/
https://www.ncbi.nlm.nih.gov/pubmed/24292196
http://dx.doi.org/10.1007/s00204-013-1161-y
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