The prevalence of obesity, Type II diabetes, and metabolic syndrome has been attributed, in part, to nutritional, psychological, and lifestyle changes in the developed world over the past century. However, other factors may contribute to this epidemic and include influences of endocrine disrupting compounds (EDCs). One such group of EDCs is flame-retardants used in household products, furniture, clothing, toys, and electronics. These EDCs are a potential ?obesogens?, which may lead to an increase or susceptibility to obesity, metabolic syndrome, and Type II diabetes in children and adults. Organophosphate flame-retardants (OPFR) are increasing in usage due to the phase-out of PBDE flame-retardants. Three of the most common OPFR are triphenyl phosphate, tricresyl phosphate, and tris(1,3-dichloro-2-propyl) phosphate. Little is known about the effects of these compounds, at environmentally relevant concentrations, on adult energy or glucose homeostasis in humans or in rodent models. Therefore, the proposed research will be focused on the effects of adult exposure to these OPFRs, in a mixture and alone, on energy and glucose homeostasis in mice. The mechanisms behind these effects are unknown but potentially involve transcriptional effects in the hypothalamus mediated by the actions of the classical estrogen receptors (ER?) and nuclear receptors (PPAR?). Our hypothesis is that OPFR impinge on the activity of nuclear receptors, both steroid and metabolic, to exert their multi-focal effects on energy and glucose homeostasis in the hypothalamus. By investigating the effects of OPFRs on energy and glucose homeostasis, we can begin to understand the impacts of these environmental contaminants on human health. Experiments will compare the effects of OPFR in the hypothalamus using a combined approach of whole-animal physiology and behavior, gene and protein expression, electrophysiology, and peptide hormone analysis in transgenic mouse strains.
In Aim 1, we will examine the effects of adult OPFR exposure on energy intake, energy expenditure, and glucose homeostasis in adults and on hypothalamic gene and protein expression via steroid and nuclear receptors.
In Aim 2, we will examine the effects of adult OPFR exposure on NPY neuronal sensitivity to peripheral peptide hormones (leptin, insulin, ghrelin) and K+ channel activity and subunit expression using state-of-the-art electrophysiology coupled with single cell-type qPCR.

Public Health Relevance

Endocrine disrupting compounds (EDC) are environmental contaminants, such as organophosphate flame- retardants, that influence of endocrine functions including energy homeostasis. This project seeks to determine the receptor-mediated effects of these flame-retardants on the arcuate nucleus, a hypothalamic center that control energy and glucose homeostasis. Understanding the cellular mechanisms involved in exposures to flame-retardants will be key to understanding the dysregulation of the homeostatic systems that lead to pathological states of energy balance such as obesity, Type II diabetes, and metabolic syndrome.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21ES027119-02
Application #
9432539
Study Section
Systemic Injury by Environmental Exposure (SIEE)
Program Officer
Schug, Thaddeus
Project Start
2017-03-01
Project End
2019-02-28
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Rutgers University
Department
Veterinary Sciences
Type
Earth Sciences/Resources
DUNS #
001912864
City
Piscataway
State
NJ
Country
United States
Zip Code
Vail, Gwyndolin; Roepke, Troy A (2018) Membrane-initiated estrogen signaling via Gq-coupled GPCR in the central nervous system. Steroids :
Walley, Sabrina N; Roepke, Troy A (2018) Perinatal exposure to endocrine disrupting compounds and the control of feeding behavior-An overview. Horm Behav 101:22-28
Acevedo-Rodriguez, A; Kauffman, A S; Cherrington, B D et al. (2018) Emerging insights into hypothalamic-pituitary-gonadal axis regulation and interaction with stress signalling. J Neuroendocrinol 30:e12590