Estradiol (E2) plays a crucial role in the maintenance of proper energy and fluid homeostasis. This key role of E2 is especially apparent in postmenopausal women who have decreased E2 levels and are at an elevated risk for obesity, obesity-related diseases, and hypertension. Unfortunately, the mechanism by which E2 regulates energy and fluid balance is still poorly understood. Rodent studies indicate that estrogens decrease food and water intake through a genomic mechanism via activation of the classical estrogen receptor subtype, estrogen receptor ? (ER??). ER?? localizes to the cell nucleus, where it alters gene expression by interacting with responsive elements on DNA. The more recent discovery that ER?? also can associate with the cell membrane and act as a surface receptor led to the appreciation that this receptor can affect gene expression through alternate, non-traditional mechanisms including activation of transcription factors such as cAMP response element binding protein (CREB). Recent studies from our laboratory demonstrate that activation of membrane-associated estrogen receptors (mER) decrease food and water intake. Accordingly, this proposal was designed to provide training in the areas of fluid intake, intercellular signaling and viral mediated genetic manipulations in addition to enhance the existing strengths of the candidate in the area of estrogen modulation of food intake. This will be accomplished, in part, by performing the proposed experiments that test the overarching hypothesis that mER decreases food and water intake by engaging intracellular signaling pathways traditionally associated with transcriptional changes. To this end, the experiments in this proposal include two aims, the first of which will test the requirement of metabotropic glutamate receptors (mGluR) in mediating the effects of mER on food and water intake.
The second aim will examine food and water intake following knockdown of mER through AAV manipulation. Next this set of experiments will test for physical interactions between mER?? and mGluR and will test the role of mGluR on the intracellular effects of E2. In addition to providing important training to the candidate that will help her transition to a career as an independent scientist, the proposed research has the potential to increase the understanding of the mechanisms by which E2 signaling influences food and water intake and has the potential to reveal more general principals of steroid effects on gene expression.
Maintaining proper body weight and fluid balance is critical to prevent obesity-related and cardiovascular diseases, respectively. Low estradiol levels in postmenopausal women are associated, however, with a greater risk for developing obesity and cardiovascular-related health problems. Therefore, understanding how estrogens modulate food and water intake in healthy animals is a crucial step in an attempt to reveal potential interventions that reduce morbidity and improve quality of life for postmenopausal women.
|Santollo, Jessica; Marshall, AnikÃ³; Curtis, Kathleen S et al. (2016) Divergent effects of ERÎ± and ERÎ² on fluid intake by female rats are not dependent on concomitant changes in AT1R expression or body weight. Am J Physiol Regul Integr Comp Physiol 311:R14-23|
|Santollo, Jessica; Daniels, Derek (2015) Multiple estrogen receptor subtypes influence ingestive behavior in female rodents. Physiol Behav 152:431-7|
|Santollo, Jessica; Daniels, Derek (2015) Control of fluid intake by estrogens in the female rat: role of the hypothalamus. Front Syst Neurosci 9:25|
|Santollo, Jessica; Daniels, Derek (2015) Activation of G protein-coupled estrogen receptor 1 (GPER-1) decreases fluid intake in female rats. Horm Behav 73:39-46|
|Santollo, Jessica; Whalen, Philip E; Speth, Robert C et al. (2014) Properly timed exposure to central ANG II prevents behavioral sensitization and changes in angiotensin receptor expression. Am J Physiol Regul Integr Comp Physiol 307:R1396-404|