Structural Malformations in the Neonatal Rat Brain Accompany Developmental Exposure to Ammonium Perchlorate

Mary E Gilbert; Katherine L O'Shaughnessy; Kiersten S Bell; Jermaine L Ford

doi:10.3390/toxics11121027

Structural Malformations in the Neonatal Rat Brain Accompany Developmental Exposure to Ammonium Perchlorate

Toxics. 2023 Dec 18;11(12):1027. doi: 10.3390/toxics11121027.

Authors

Mary E Gilbert¹, Katherine L O'Shaughnessy¹, Kiersten S Bell², Jermaine L Ford³

Affiliations

¹ Centre for Public Health and Environmental Assessment, Office of Research and Development, Environmetal Protection Agency, Research Triangle Park, NC 27709, USA.
² College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
³ National Center for Computational Toxicology, Office of Research and Development, Environmental Protection Agency, Research Triangle Park, NC 27709, USA.

Abstract

Environmental contaminants are often flagged as thyroid system disruptors due to their actions to reduce serum thyroxine (T4) in rodent models. The presence of a periventricular heterotopia (PVH), a brain malformation resulting from T4 insufficiency, has been described in response to T4 decrements induced by pharmaceuticals that reduce the hormone synthesis enzyme thyroperoxidase. In this report, we extend these observations to the environmental contaminant perchlorate, an agent that interferes with thyroid status by inhibiting iodine uptake into the thyroid gland. Pregnant rat dams were administered perchlorate in their drinking water (0, 30, 100, 300, 1000 ppm) from gestational day (GD) 6 until the weaning of pups on postnatal day (PN) 21. Serum T4 was reduced in dams and fetuses in late gestation and remained lower in lactating dams. Pup serum and brain T4, however, were not reduced beyond PN0, and small PVHs were evident in the brains of offspring when assessed on PN14. To emulate the developmental time window of the brain in humans, a second study was conducted in which pups from perchlorate-exposed dams were administered perchlorate orally from PN0 to PN6. This treatment reduced serum and brain T4 in the pup and resulted in large PVH. A third study extended the period of serum and brain TH suppression in pups by coupling maternal perchlorate exposure with maternal dietary iodine deficiency (ID). No PVHs were evident in the pups from ID dams, small PVHs were observed in the offspring of dams exposed to 300 ppm of perchlorate, and very large PVHs were present in the brains of pups born to dams receiving ID and perchlorate. These findings underscore the importance of the inclusion of serum hormone profiles in pregnant dams and fetuses in in vivo screens for thyroid-system-disrupting chemicals and indicate that chemical-induced decreases in fetal rat serum that resolve in the immediate postnatal period may still harbor considerable concern for neurodevelopment in humans.

Keywords: AOP; brain; development; neurotoxicity; perchlorate; thyroid hormone.

Grants and funding

This research was conducted at the US EPA and received no external funding.