Abstract

Substantial evidence indicates that bisphenol A (BPA), a ubiquitous environmental chemical used in the synthesis of polycarbonate plastics and epoxy resins, can impair brain development. Clinical and epidemiological studies exploring potential connections between BPA and neurodevelopmental disorders in humans have repeatedly identified correlations between early BPA exposure and developmental disorders, such as attention deficit/hyperactivity disorder and autism spectrum disorder. Investigations using invertebrate and vertebrate animal models have revealed that developmental exposure to BPA can impair multiple aspects of neuronal development, including neural stem cell proliferation and differentiation, synapse formation, and synaptic plasticity—neuronal phenotypes that are thought to underpin the fundamental changes in behavior-associated neurodevelopmental disorders. Consistent with neuronal phenotypes caused by BPA, behavioral analyses of BPA-treated animals have shown significant impacts on behavioral endophenotypes related to neurodevelopmental disorders, including altered locomotor activity, learning and memory deficits, and anxiety-like behavior. To contextualize the correlations between BPA and neurodevelopmental disorders in humans, this review summarizes the current literature on the developmental neurotoxicity of BPA in laboratory animals with an emphasis on neuronal phenotypes, molecular mechanisms, and behavioral outcomes. The collective works described here predominantly support the notion that gestational exposure to BPA should be regarded as a risk factor for neurodevelopmental disorders.

Highlights

  • Publisher’s Note: MDPI stays neutralBisphenol A (BPA, 2,2-bis (40 -hydroxyphenyl) propane), a ubiquitous chemical used in the synthesis of polycarbonate plastic and epoxy resins, is taking shape as a risk factor for neurodevelopmental disorders (NDDs)

  • NDDs refer to a heterogeneous group of nervous system disorders caused by changes in brain development, including autism spectrum disorder (ASD), attention deficit/hyperactivity disorder (ADHD), intellectual disability (ID), learning disabilities, cerebral palsy, seizure disorders, and impairments in vision and hearing

  • This review described the neurodevelopmental impacts—molecular, cellular, and behavioral—resulting from early exposure to bisphenol A (BPA) in organisms spanning the animal kingdom, from invertebrates to mammals

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Summary

Introduction

Bisphenol A (BPA, 2,2-bis (40 -hydroxyphenyl) propane), a ubiquitous chemical used in the synthesis of polycarbonate plastic and epoxy resins, is taking shape as a risk factor for neurodevelopmental disorders (NDDs). NDDs [7–9], BPA has garnered increasing attention over the past fifteen years for its ability to disrupt brain development. The aim of this review is to summarize studies that have delineated neurodevelopmental consequences of early (prenatal or perinatal) BPA exposure in animal models in an effort to illuminate the mechanisms by which it may impede human brain development. Consistent with the brain being a commonly reported target of EDCs [42], early BPA exposure is associated with behavioral impairment and NDDs in children [7–9]. Longitudinal studies that measured maternal BPA exposure levels during pregnancy and subsequently examined the children identified positive correlations between BPA and ADHD-related symptoms [43], learning deficits [44,45], externalizing behaviors [46], and anxiety and depression [47].

Neural Stem Cell Proliferation and Differentiation Are Affected by BPA
Synapse Formation Is Disrupted by BPA
Synaptic Plasticity Is Impaired by BPA
Behavior Is Impacted by BPA
Findings
Conclusions
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