To fully understand changes in cognitive function during aging, it is necessary to understand how hormones that decline with age normally regulate and maintain structural and functional plasticity and resilience of the adult brain. Estradiol (E) is the best-studied hormone with respect to protection from cognitive decline and effects of stroke and risk for Alzheimer's disease in women. Yet, we are only beginning to understand how the aging brain responds to E at the cellular, molecular and anatomical levels and how E regulated plasticity changes with age. A major new direction in E action is the investigation of "non-genomic"signaling pathways by which E influences the functions of many cells in the brain and other organs. These pathways affect cell survival, cytoskeletal reorganization, protein synthesis, among other processes, as part of maintaining 'healthy brain cell functions" but they can be lost or severely impaired as the brain ages. The main objective of this project in support of the overall Program Project, focusing on hippocampus, is three-fold: first, to carry out in vitro studies of the E molecular mechanisms underiying E regulation of "non-genomic" signaling processes;second, to determine the relevance of these pathways to such spine synapse formation and maturation (SSF/IVI) via immunocytochemical and ultrastructural studies on the adult rat hippocampus;third, to determine the relevance of these pathways to the loss with aging of E effects as spine synapse formation and maturation (SSF/M)using in vitro and in vivo approaches. In carrying out these goals, collaborative studies within the PPG will determine the relevance of these mechanisms to the studies of the age-related decline in cognitive as well as neuroendocrine function in the aging rat and primate brain which are being studied in other components of this program project. Our central hypothesis is that age-related failure of E treatment to increase the number of synapses in CAI region of the hippocampus may be due to changes in the molecular profile of axospinous synapses with respect to signaling pathway that participate in spine synapse formation and maturation (SSF/M) in response to E. To achieve this, we intend to, first, determine the signaling pathways and estrogen receptor involvement in NR2B phosphorylation and if aging results in a reduction of pNR2b in synaptic compartments;second, to determine how E activates the key signaling pathway, PISK-kinase, in the dendritic spine, and when and where this activation is lost in dendritic spines of the aging brain;third, to determine the role of the actin regulating protein, cortactin, in SSF/M and the rate- limiting role of cortactin in the age-related loss of E-induced SSF/M. Knowledge gained in these studies will focus preventative therapies on the key age-sensitive signaling pathways and molecules.
Age-related cognitive decline is a serious problem. To fully understand changes in cognitive function during aging, we must understand how hormones that decline with age normally regulate and maintain structural and functional plasticity and resilience of the adult brain. We study actions of estradiol (E), known to protect from cognitive decline and effects of stroke and risk for Alzheimer's disease in women;knowledge gained in these studies will focus preventative therapies on the key age-sensitive signaling pathways and molecules.
|Naugle, Michelle M; Lozano, Sateria A; Guarraci, Fay A et al. (2016) Age and Long-Term Hormone Treatment Effects on the Ultrastructural Morphology of the Median Eminence of Female Rhesus Macaques. Neuroendocrinology 103:650-64|
|Garcia, Alexandra N; Depena, Christina K; Yin, Weiling et al. (2016) Testing the critical window of estradiol replacement on gene expression of vasopressin, oxytocin, and their receptors, in the hypothalamus of aging female rats. Mol Cell Endocrinol 419:102-12|
|Almey, Anne; Milner, Teresa A; Brake, Wayne G (2016) Estrogen receptor Î± and G-protein coupled estrogen receptor 1 are localized to GABAergic neurons in the dorsal striatum. Neurosci Lett 622:118-23|
|Mazid, Sanoara; Hall, Baila S; Odell, Shannon C et al. (2016) Sex differences in subcellular distribution of delta opioid receptors in the rat hippocampus in response to acute and chronic stress. Neurobiol Stress 5:37-53|
|Marques-Lopes, Jose; Lynch, Mary-Katherine; Van Kempen, Tracey A et al. (2015) Female protection from slow-pressor effects of angiotensin II involves prevention of ROS production independent of NMDA receptor trafficking in hypothalamic neurons expressing angiotensin 1A receptors. Synapse 69:148-65|
|Yin, Weiling; Sun, Zengrong; Mendenhall, John M et al. (2015) Expression of Vesicular Glutamate Transporter 2 (vGluT2) on Large Dense-Core Vesicles within GnRH Neuroterminals of Aging Female Rats. PLoS One 10:e0129633|
|Waters, Elizabeth M; Thompson, Louisa I; Patel, Parth et al. (2015) G-protein-coupled estrogen receptor 1 is anatomically positioned to modulate synaptic plasticity in the mouse hippocampus. J Neurosci 35:2384-97|
|Yin, Weiling; Maguire, Sean M; Pham, Brian et al. (2015) Testing the Critical Window Hypothesis of Timing and Duration of Estradiol Treatment on Hypothalamic Gene Networks in Reproductively Mature and Aging Female Rats. Endocrinology 156:2918-33|
|Almey, Anne; Milner, Teresa A; Brake, Wayne G (2015) Estrogen receptors in the central nervous system and their implication for dopamine-dependent cognition in females. Horm Behav 74:125-38|
|Hara, Yuko; Waters, Elizabeth M; McEwen, Bruce S et al. (2015) Estrogen Effects on Cognitive and Synaptic Health Over the Lifecourse. Physiol Rev 95:785-807|
Showing the most recent 10 out of 120 publications