@article{hicks_sullivan_cao_sluzas_rebuli_patisaul_2016, title={Interaction of bisphenol A (BPA) and soy phytoestrogens on sexually dimorphic sociosexual behaviors in male and female rats}, volume={84}, ISSN={["1095-6867"]}, DOI={10.1016/j.yhbeh.2016.06.010}, abstractNote={Concerns have been raised regarding the potential for endocrine disrupting compounds (EDCs) to alter brain development and behavior. Developmental exposure to bisphenol A (BPA), a ubiquitous EDC, has been linked to altered sociosexual and mood-related behaviors in various animal models and children but effects are inconsistent across laboratories and animal models creating confusion about potential risk in humans. Exposure to endocrine active diets, such as soy, which is rich in phytoestrogens, may contribute to this variability. Here, we tested the individual and combined effects of low dose oral BPA and soy diet or the individual isoflavone genistein (GEN; administered as the aglycone genistin (GIN)) on rat sociosexual behaviors with the hypothesis that soy would obfuscate any BPA-related effects. Social and activity levels were unchanged by developmental exposure to BPA but soy diet had sex specific effects including suppressed novelty preference, and open field exploration in females. The data presented here reinforce that environmental factors, including anthropogenic chemical exposure and hormone active diets, can shape complex behaviors and even reverse expected sex differences.}, journal={HORMONES AND BEHAVIOR}, author={Hicks, Kimani D. and Sullivan, Alana W. and Cao, Jinyan and Sluzas, Emily and Rebuli, Meghan and Patisaul, Heather B.}, year={2016}, month={Aug}, pages={121–126} }
 @article{sullivan_beach_stetzik_perry_alyssa s. d'addezio_cushing_patisaul_2014, title={A Novel Model for Neuroendocrine Toxicology: Neurobehavioral Effects of BPA Exposure in a Prosocial Species, the Prairie Vole (Microtus ochrogaster)}, volume={155}, ISSN={["1945-7170"]}, DOI={10.1210/en.2014-1379}, abstractNote={Abstract}, number={10}, journal={ENDOCRINOLOGY}, author={Sullivan, Alana W. and Beach, Elsworth C. and Stetzik, Lucas A. and Perry, Amy and Alyssa S. D'Addezio and Cushing, Bruce S. and Patisaul, Heather B.}, year={2014}, month={Oct}, pages={3867–3881} }
 @article{patisaul_mabrey_adewale_sullivan_2014, title={Soy but not bisphenol A (BPA) induces hallmarks of polycystic ovary syndrome (PCOS) and related metabolic co-morbidities in rats}, volume={49}, ISSN={["0890-6238"]}, DOI={10.1016/j.reprotox.2014.09.003}, abstractNote={Polycystic ovarian syndrome (PCOS) is the most common female endocrine disorder with a prevalence as high as 8-15% depending on ethnicity and the diagnostic criteria employed. The basic pathophysiology and mode of inheritance remain unclear, but environmental factors such as diet, stress and chemical exposures are thought to be contributory. Developmental exposure to endocrine disrupting compounds (EDCs) have been hypothesized to exacerbate risk, in part because PCOS hallmarks and associated metabolic co-morbidities can be reliably induced in animal models by perinatal androgen exposure. Here we show that lifetime exposure to a soy diet, containing endocrine active phytoestrogens, but not developmental exposure (gestational day 6-lactational day 40) to the endocrine disrupting monomer bisphenol A (BPA), can induce key features of PCOS in the rat; results which support the hypothesis that hormonally active diets may contribute to risk when consumed throughout gestation and post-natal life.}, journal={REPRODUCTIVE TOXICOLOGY}, author={Patisaul, Heather B. and Mabrey, Natalie and Adewale, Heather B. and Sullivan, Alana W.}, year={2014}, month={Nov}, pages={209–218} }
 @article{patisaul_sullivan_radford_walker_adewale_winnik_coughlin_buckley_gore_2012, title={Anxiogenic Effects of Developmental Bisphenol A Exposure Are Associated with Gene Expression Changes in the Juvenile Rat Amygdala and Mitigated by Soy}, volume={7}, ISSN={["1932-6203"]}, DOI={10.1371/journal.pone.0043890}, abstractNote={Early life exposure to Bisphenol A (BPA), a component of polycarbonate plastics and epoxy resins, alters sociosexual behavior in numerous species including humans. The present study focused on the ontogeny of these behavioral effects beginning in adolescence and assessed the underlying molecular changes in the amygdala. We also explored the mitigating potential of a soy-rich diet on these endpoints. Wistar rats were exposed to BPA via drinking water (1 mg/L) from gestation through puberty, and reared on a soy-based or soy-free diet. A group exposed to ethinyl estradiol (50 µg/L) and a soy-free diet was used as a positive estrogenic control. Animals were tested as juveniles or adults for anxiety-like and exploratory behavior. Assessment of serum BPA and genistein (GEN), a soy phytoestrogen, confirmed that internal dose was within a human-relevant range. BPA induced anxiogenic behavior in juveniles and loss of sexual dimorphisms in adult exploratory behavior, but only in the animals reared on the soy-free diet. Expression analysis revealed a suite of genes, including a subset known to mediate sociosexual behavior, associated with BPA-induced juvenile anxiety. Notably, expression of estrogen receptor beta (Esr2) and two melanocortin receptors (Mc3r, Mc4r) were downregulated. Collectively, these results show that behavioral impacts of BPA can manifest during adolescence, but wane in adulthood, and may be mitigated by diet. These data also reveal that, because ERβ and melanocortin receptors are crucial to their function, oxytocin/vasopressin signaling pathways, which have previously been linked to human affective disorders, may underlie these behavioral outcomes.}, number={9}, journal={PLOS ONE}, author={Patisaul, Heather B. and Sullivan, Alana W. and Radford, Meghan E. and Walker, Deena M. and Adewale, Heather B. and Winnik, Bozena and Coughlin, Janis L. and Buckley, Brian and Gore, Andrea C.}, year={2012}, month={Sep} }
 @article{sullivan_hamilton_patisaul_2011, title={Neonatal agonism of ERβ impairs male reproductive behavior and attractiveness}, volume={60}, ISSN={0018-506X}, url={http://dx.doi.org/10.1016/j.yhbeh.2011.04.006}, DOI={10.1016/j.yhbeh.2011.04.006}, abstractNote={The organization of the developing male rodent brain is profoundly influenced by endogenous steroids, most notably estrogen. This process may be disrupted by estrogenic endocrine disrupting compounds (EDCs) resulting in altered sex behavior and the capacity to attract a mate in adulthood. To better understand the relative role each estrogen receptor (ER) subtype (ERα and ERβ) plays in mediating these effects, we exposed male Long Evans rats to estradiol benzoate (EB, 10 μg), vehicle, or agonists specific for ERβ (DPN, 1 mg/kg) or ERα (PPT, 1 mg/kg) daily for the first four days of life, and then assessed adult male reproductive behavior and attractiveness via a partner preference paradigm. DPN had a greater adverse impact than PPT on reproductive behavior, suggesting a functional role for ERβ in the organization of these male-specific behaviors. Therefore the impact of neonatal ERβ agonism was further investigated by repeating the experiment using vehicle, EB and additional DPN doses (0.5 mg/kg, 1 mg/kg, and 2 mg/kg bw). Exposure to DPN suppressed male reproductive behavior and attractiveness in a dose dependent manner. Finally, males were exposed to EB or an environmentally relevant dose of genistein (GEN, 10 mg/kg), a naturally occurring xenoestrogen, which has a higher relative binding affinity for ERβ than ERα. Sexual performance was impaired by GEN but not attractiveness. In addition to suppressing reproductive behavior and attractiveness, EB exposure significantly lowered the testis to body weight ratio, and circulating testosterone levels. DPN and GEN exposure only impaired behavior, suggesting that disrupted androgen secretion does not underlie the impairment.}, number={2}, journal={Hormones and Behavior}, publisher={Elsevier BV}, author={Sullivan, Alana W. and Hamilton, Peter and Patisaul, Heather B.}, year={2011}, month={Jul}, pages={185–194} }
 @article{losa_todd_sullivan_cao_mickens_patisaul_2011, title={Neonatal exposure to genistein adversely impacts the ontogeny of hypothalamic kisspeptin signaling pathways and ovarian development in the peripubertal female rat}, volume={31}, ISSN={["0890-6238"]}, DOI={10.1016/j.reprotox.2010.10.002}, abstractNote={Neonatal exposure to estrogenic endocrine disrupting compounds (EDCs) can advance pubertal onset and induce premature anestrous in female rats. It was recently discovered that hypothalamic kisspeptin (KISS) signaling pathways are sexually dimorphic and regulate both the timing of pubertal onset and estrous cyclicity. Thus we hypothesized that disrupted sex specific ontogeny of KISS signaling pathways might be a mechanism underlying these EDC effects. We first established the sex specific development of KISS gene expression, cell number and neural fiber density across peripuberty in the anteroventral periventricular nucleus (AVPV) and arcuate nucleus (ARC), hypothesizing that the sexually dimorphic aspects of KISS signaling would be most vulnerable to EDCs. We next exposed female rats to the phytoestrogen genistein (GEN, 1 or 10 mg/kg bw), estradiol benzoate (EB, 10 μg), or vehicle from post natal day (P) 0–3 via subcutaneous (sc) injection. Animals were sacrificed on either P21, 24, 28, or 33 (n = 5–14 per group at each age). Vaginal opening was significantly advanced by EB and the higher dose of GEN compared to control animals and was accompanied by lower numbers of KISS immunoreactive fibers in the AVPV and ARC. Ovarian morphology was also assessed in all age groups for the presence of multiple oocyte follicles (MOFs). The number of MOFs decreased over time in each group, and none were observed in control animals by P24. MOFs were still present, however, in the EB and 10 mg/kg GEN groups beyond P24 indicating a disruption in the timing of ovarian development.}, number={3}, journal={REPRODUCTIVE TOXICOLOGY}, author={Losa, Sandra M. and Todd, Karina L. and Sullivan, Alana W. and Cao, Jinyan and Mickens, Jillian A. and Patisaul, Heather B.}, year={2011}, month={Apr}, pages={280–289} }