Browsing by Subject "Polychlorinated biphenyls"

Now showing 1 - 4 of 4

Bioavailability and trophic transfer of PAHs and PCBs
(2007-05) Drake, Brian Ely, 1983-; Reible, Danny D.
Evaluating organic compound sorption to several materials to assess their potential as amendments to improve in-situ capping of contaminated sediments
(2011-05) Dunlap, Patrick John; Reible, Danny D.; Liljestrand, Howard
Contaminated sediments represent a common environmental problem because they can sequester large quantities of contaminants which can remain long after the source of pollution has been removed. From the sediment these hazardous compounds are released into the sediment porewater where it can partition into organisms in the sediment and bioaccumulate up the food web; leading to an ecological and human health concern. The objective of this work is to investigate an emerging option in contaminated sediment remediation; specifically an option for in-situ treatment known as active capping. Conventional capping uses clean sediment or sands to separate contaminated sediment from overlying water and biota. Active capping is the use of a sorptive amendment to such a cap to improve its effectiveness. This work focuses on granular materials as direct amendments to conventional caps including; granular activated carbon (GAC), iron/palladium amended GAC, alumina pillared clay, rice husk char, and organically modified clays. All materials were investigated in batch sorption tests of benzene, chlorobenzene, and naphthalene in DI water. Additionally porewaters from three sites were extruded and the concentrations of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were measured. At Manistique Harbor and Ottawa River PCBs were identified as the primary contaminant of concern while PAHs were the contaminant of concern at the Grand Calumet River. At these sites a solvent extraction method was used to analyze the sediment concentrations of the contaminants of concern. From the former batch tests activated carbon and a commercially available organoclay were chosen for further investigation. This includes PAHs in batch sorption tests using extruded sediment porewater to investigate matrix effects, and PCB sorption in distilled water.
Mechanisms for endocrine disrupting chemical action on sexual differentiation of the rat brain
(2010-12) Dickerson, Sarah Michelle; Gore, Andrea C., 1964-; Crews, David P.; Duvauchelle, Christine L.; Mills, Edward M.; Thomas, Peter
Endocrine disrupting chemicals (EDCs) are a class of environmental toxicants, of both natural and synthetic origin, that interfere with normal endocrine function. Exposure to EDCs during susceptible periods of development, particularly embryogenesis, can result in profound neurological and reproductive deficits. While the impact of developmental exposure to EDCs on reproductive function and behavior has been much studied, the underlying mechanisms responsible for these observed effects are not well understood. The goal of the research detailed in this dissertation is to elucidate the cellular and molecular targets by which a representative class of EDCs, polychlorinated biphenyls (PCBs), disrupts normal reproductive neuroendocrine function. My specific hypothesis is that PCBs cause changes in sexually dimorphic brain regions underlying sex-specific reproductive physiology and behavior through the perturbation of normal developmental apoptosis, with long-term consequences for reproductive success. The studies detailed herein focus on three areas which contribute to an understanding of the effects of PCBs on neuroendocrine reproductive function: (1) the in vitro effects of PCBs on a neuroendocrine cell line, (2) developmental effects of PCBs on the gestationally exposed F1 generation, and (3) the physiological consequences of these developmental alterations for adult reproductive function. In the first section of this dissertation, the neurotoxic and endocrine disrupting effects of PCBs on a representative developing neuroendocrine cell model, the GT1-7 GnRH cell line, are investigated in time- and dose-response experiments. Treatment and dose-dependent effects are observed for GnRH peptide concentrations, cell viability, apoptotic and necrotic cell death, and caspase activation. In general, GnRH peptide levels are suppressed by high doses and longer durations of PCBs, and elevated at low doses and shorter time points. The suppression of GnRH peptide levels was partially reversed in cultures co-treated with the estrogen receptor antagonist ICI 182,780. All PCBs tested reduced viability and increased both apoptotic and necrotic cell death. The second section of this dissertation examines whether prenatal PCB exposure alters normal neuroendocrine development in the F1 generation, including sexual differentiation of the brain. Disruption of hypothalamic development is detectable as early as the day after birth (postnatal day (P) 1), as indicated by abnormal programmed cell death, and alterations in neuroendocrine gene and protein expression. The third section discusses the physiological impact of developmental PCB exposure on reproductive maturation and adult neuroendocrine function. Pubertal onset is advanced and estrous cyclicity irregular in PCB endocrine-disrupted females. Furthermore, sexual differentiation of female neuroendocrine systems is masculinized/defeminized. Collectively, these results suggest that the disrupted sexual differentiation of the POA can be detected as early as the day after birth, effects that may underlie the adult reproductive phenotype.
The effects of gestational exposure to endocrine-disrupting chemicals on the adult social behavior in male and female rats
(2018-06-13) Reilly, Michael Patrick; Gore, Andrea C., 1964-; Crews, David; Vasquez, Karen; Dominguez, Juan; Richburg, John
Endocrine disrupting chemicals (EDC) exposures during critical periods of development influence neuronal development and the manifestation of sexually dimorphic behaviors that emerge in adulthood. Among these behaviors, social information processing is sexually dimorphic and regulated by sex steroids. Oxytocin and vasopressin serve as primary neurotransmitters mediating these behaviors; these neuroendocrine circuits are hormone sensitive and potential targets of prenatal EDC exposures. In dissertation, I assess the effects of gestational exposure to EDCs on the social behavior of male and females later in adulthood. A weakly estrogenic PCB mixture, Aroclor 1221, was administered to pregnant Sprague-Dawley rat dams during the time when the hypothalamus undergoes sexual differentiation. The brains of these animals were also used to quantify the presence of oxytocin or vasopressin in the two main regions of production: the paraventricular nucleus (PVN) and the supraoptic nucleus (SON). Another experiment extended this treatment paradigm to encompass a longer period of gestational development, added another EDC treatment group (Vinclozolin), and looked at similar behavioral outcomes. Lastly, I provide a novel way of modeling complex social behaviors in a laboratory setting. Through all of this work, we show that the sexes are differentially susceptible to endocrine disruption by PCBs or vinclozolin. Additionally, we provide evidence that the traditional choice models of social behavior in the rodent may not be reflective of how an animal behaves in a more complex, naturalistic, environment.