Maternal organophosphate flame retardant exposure alters the developing mesencephalic dopamine system in fetal rat

Author:

Newell Andrew J1,Kapps Victoria A1,Cai Yuheng23,Rai Mani Ratnam23,St. Armour Genevieve1,Horman Brian M1,Rock Kylie D1,Witchey Shannah K1,Greenbaum Alon23,Patisaul Heather B14ORCID

Affiliation:

1. Department of Biological Sciences, North Carolina State University , Raleigh, North Carolina 27695, USA

2. Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University , Raleigh, North Carolina 27606, USA

3. Comparative Medicine Institute, North Carolina State University , Raleigh, North Carolina 27606, USA

4. Center for Human Health and the Environment, North Carolina State University , Raleigh, North Carolina 27695, USA

Abstract

AbstractOrganophosphate flame retardants (OPFRs) have become the predominant substitution for legacy brominated flame retardants but there is concern about their potential developmental neurotoxicity (DNT). OPFRs readily dissociate from the fireproofed substrate to the environment, and they (or their metabolites) have been detected in diverse matrices including air, water, soil, and biota, including human urine and breastmilk. Given this ubiquitous contamination, it becomes increasingly important to understand the potential effects of OPFRs on the developing nervous system. We have previously shown that maternal exposure to OPFRs results in neuroendocrine disruption, alterations to developmental metabolism of serotonin (5-HT) and axonal extension in male fetal rats, and potentiates adult anxiety-like behaviors. The development of the serotonin and dopamine systems occur in parallel and interact, therefore, we first sought to enhance our prior 5-HT work by first examining the ascending 5-HT system on embryonic day 14 using whole mount clearing of fetal heads and 3-dimensional (3D) brain imaging. We also investigated the effects of maternal OPFR exposure on the development of the mesocortical dopamine system in the same animals through 2-dimensional and 3D analysis following immunohistochemistry for tyrosine hydroxylase (TH). Maternal OPFR exposure induced morphological changes to the putative ventral tegmental area and substantia nigra in both sexes and reduced the overall volume of this structure in males, whereas 5-HT nuclei were unchanged. Additionally, dopaminergic axogenesis was disrupted in OPFR exposed animals, as the dorsoventral spread of ventral telencephalic TH afferents were greater at embryonic day 14, while sparing 5-HT fibers. These results indicate maternal exposure to OPFRs alters the development trajectory of the embryonic dopaminergic system and adds to growing evidence of OPFR DNT.

Funder

Comparative Medicine Institute of North Carolina State University

National Institute of Environmental Health Sciences

Publisher

Oxford University Press (OUP)

Subject

Toxicology

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