The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex

Bisphenol-A (BPA) is a monomer used in the production of polycarbonate plastics, epoxies and resins and is present in many common household objects ranging from water bottles, can linings, baby bottles, and dental resins. BPA exposure has been linked to numerous negative health effects throughout th...

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Main Authors: Emily Anna Kelly, Lisa A Opanashuk, Ania K Majewska
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-10-01
Series:Frontiers in Neuroanatomy
Subjects:
V1
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnana.2014.00117/full
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spelling doaj-c887ef82697d48699bf5a05e738695bb2020-11-24T21:01:33ZengFrontiers Media S.A.Frontiers in Neuroanatomy1662-51292014-10-01810.3389/fnana.2014.00117103326The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory CortexEmily Anna Kelly0Lisa A Opanashuk1Ania K Majewska2University of RochesterUniversity of RochesterUniversity of RochesterBisphenol-A (BPA) is a monomer used in the production of polycarbonate plastics, epoxies and resins and is present in many common household objects ranging from water bottles, can linings, baby bottles, and dental resins. BPA exposure has been linked to numerous negative health effects throughout the body, although the mechanisms of BPA action on the developing brain are still poorly understood. In this study, we sought to investigate whether low dose BPA exposure during a developmental phase when brain connectivity is being organized can cause long-term deleterious effects on brain function and plasticity that outlast the BPA exposure. Lactating dams were orally exposed to 25 g/kg/day of BPA (one half the U.S. Environmental Protection Agency’s 50 g/kg/day rodent dose reference) or vehicle alone from postnatal day (P)5 to P21. Pups exposed to BPA in their mother’s milk exhibited deficits in activity-dependent plasticity in the visual cortex during the visual critical period (P28). To determine the possible mechanisms underlying BPA action, we used immunohistochemistry to examine histological markers known to impact cortical maturity and developmental plasticity and quantified cortical dendritic spine density, morphology and dynamics. While we saw no changes in parvalbumin neuron density, myelin basic protein expression or microglial density in BPA-exposed animals, these mice showed increases in spine density on apical dendrites in cortical layer 5 neurons but no significant alternations in morphological parameters. Taken together our results suggest that exposure to very low levels of BPA during a critical period of brain development can have profound consequences for the normal wiring of sensory circuits and their plasticity later in life.http://journal.frontiersin.org/Journal/10.3389/fnana.2014.00117/fullSpineplasticityDendriteV1Bisphenol-Aocular dominance
collection DOAJ
language English
format Article
sources DOAJ
author Emily Anna Kelly
Lisa A Opanashuk
Ania K Majewska
spellingShingle Emily Anna Kelly
Lisa A Opanashuk
Ania K Majewska
The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
Frontiers in Neuroanatomy
Spine
plasticity
Dendrite
V1
Bisphenol-A
ocular dominance
author_facet Emily Anna Kelly
Lisa A Opanashuk
Ania K Majewska
author_sort Emily Anna Kelly
title The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
title_short The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
title_full The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
title_fullStr The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
title_full_unstemmed The Effects of Postnatal Exposure to Low-Dose Bisphenol-A on Activity-Dependent Plasticity in the Mouse Sensory Cortex
title_sort effects of postnatal exposure to low-dose bisphenol-a on activity-dependent plasticity in the mouse sensory cortex
publisher Frontiers Media S.A.
series Frontiers in Neuroanatomy
issn 1662-5129
publishDate 2014-10-01
description Bisphenol-A (BPA) is a monomer used in the production of polycarbonate plastics, epoxies and resins and is present in many common household objects ranging from water bottles, can linings, baby bottles, and dental resins. BPA exposure has been linked to numerous negative health effects throughout the body, although the mechanisms of BPA action on the developing brain are still poorly understood. In this study, we sought to investigate whether low dose BPA exposure during a developmental phase when brain connectivity is being organized can cause long-term deleterious effects on brain function and plasticity that outlast the BPA exposure. Lactating dams were orally exposed to 25 g/kg/day of BPA (one half the U.S. Environmental Protection Agency’s 50 g/kg/day rodent dose reference) or vehicle alone from postnatal day (P)5 to P21. Pups exposed to BPA in their mother’s milk exhibited deficits in activity-dependent plasticity in the visual cortex during the visual critical period (P28). To determine the possible mechanisms underlying BPA action, we used immunohistochemistry to examine histological markers known to impact cortical maturity and developmental plasticity and quantified cortical dendritic spine density, morphology and dynamics. While we saw no changes in parvalbumin neuron density, myelin basic protein expression or microglial density in BPA-exposed animals, these mice showed increases in spine density on apical dendrites in cortical layer 5 neurons but no significant alternations in morphological parameters. Taken together our results suggest that exposure to very low levels of BPA during a critical period of brain development can have profound consequences for the normal wiring of sensory circuits and their plasticity later in life.
topic Spine
plasticity
Dendrite
V1
Bisphenol-A
ocular dominance
url http://journal.frontiersin.org/Journal/10.3389/fnana.2014.00117/full
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