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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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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