In order to fully understand changes in brain function during aging, it is necessary to understand how hormones that decline with age, such as estradiol (E) and dehydroepiandrosterone (DHEA) maintain the normal plasticity and resilience of the adult brain. Estradiol is the best studied hormone with respect to cognitive decline and Alzheimer's disease; yet, even then, we are largely ignorant about how the aging brain responds to E at the cellular and at anatomical levels, or whether E (and DHEA) have neuroprotective actions that are related to their ability to regulate plasticity. This project utilizes cell culture of embryonic hippocampal neurons that are allowed to mature for at least 10d in vitro to differentiate and establish connections among neurons with an environment of glial cells. It uses not only cell culture, with immunocytochemistry and in situ hybridization, but also employs the technique of differential display to identify novel and known genes that are activated during the induction of resilience and synapse formation. The project has a three-fold objective: First, to study the processes at the cellular and molecular level by which estradiol (E) causes synapse formation in hippocampal neurons; this will be relevant to the studies of the hypothesized age-related decline in E- induced hippocampal synapse formation in the aging rat and primate brain which are being studied in other components of this program project; Second, to study how the conditions of E treatment that results in synapse formation alter the response of the hippocampus to excitotoxic damage, and , in this connection, Third, to investigate the possible synergistic neuroprotective effects of another steroid that declines with age, dehydroepiandrosterone (DHEA). DHEA has been reported to block NMDA-induced excitotoxicity and to do so, at least in part, by acting on glial cells, which are also responsive to estrogens. Glial cells also participate in E-induced synapse formation and the information gained in these studies will illuminate this aspect as well.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG016765-02
Application #
6299414
Study Section
Project Start
2000-04-01
Project End
2001-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
2
Fiscal Year
2000
Total Cost
$642,420
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Baxter, Mark G; Santistevan, Anthony C; Bliss-Moreau, Eliza et al. (2018) Timing of cyclic estradiol treatment differentially affects cognition in aged female rhesus monkeys. Behav Neurosci 132:213-223
Crimins, Johanna L; Puri, Rishi; Calakos, Katina C et al. (2018) Synaptic distributions of pS214-tau in rhesus monkey prefrontal cortex are associated with spine density, but not with cognitive decline. J Comp Neurol :
Milham, Michael P; Ai, Lei; Koo, Bonhwang et al. (2018) An Open Resource for Non-human Primate Imaging. Neuron 100:61-74.e2
Motley, Sarah E; Grossman, Yael S; Janssen, William G M et al. (2018) Selective Loss of Thin Spines in Area 7a of the Primate Intraparietal Sulcus Predicts Age-Related Working Memory Impairment. J Neurosci 38:10467-10478
Bliss-Moreau, Eliza; Baxter, Mark G (2018) Estradiol treatment in a nonhuman primate model of menopause preserves affective reactivity. Behav Neurosci 132:224-229
Garcia, Alexandra N; Depena, Christina; Bezner, Kelsey et al. (2018) The timing and duration of estradiol treatment in a rat model of the perimenopause: Influences on social behavior and the neuromolecular phenotype. Horm Behav 97:75-84
Beckman, Danielle; Baxter, Mark G; Morrison, John H (2018) Future directions in animal models of Alzheimer's disease. J Neurosci Res 96:1829-1830
McEwen, Bruce S; Milner, Teresa A (2017) Understanding the broad influence of sex hormones and sex differences in the brain. J Neurosci Res 95:24-39
Nutsch, Victoria L; Bell, Margaret R; Will, Ryan G et al. (2017) Aging and estradiol effects on gene expression in the medial preoptic area, bed nucleus of the stria terminalis, and posterodorsal medial amygdala of male rats. Mol Cell Endocrinol 442:153-164
Garcia, Alexandra N; Bezner, Kelsey; Depena, Christina et al. (2017) The effects of long-term estradiol treatment on social behavior and gene expression in adult female rats. Horm Behav 87:145-154

Showing the most recent 10 out of 132 publications