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According to our matching algorithm, Rachel Pearcy Tillage is the likely recipient of the following grants.
| Years |
Recipients |
Code |
Title / Keywords |
Matching
score |
| 2018 — 2020 |
Pearcy, Rachel |
F31Activity Code Description:
To provide predoctoral individuals with supervised research training in specified health and health-related areas leading toward the research degree (e.g., Ph.D.). |
The Role of Locus Coeruleus Hyperactivity and Galanin in Depressive Behavior
PROJECT SUMMARY Depression is a highly prevalent disorder, yet reliable treatments are currently lacking for many people. Because the basic etiology of depression is not yet known, it is currently impossible to create therapeutics that target its underlying neurobiological causes. Evidence from previous research suggests that dysregulated hyperactivity of the noradrenergic locus coeruleus (LC), a brainstem nucleus that has been implicated in neuropsychiatric disorders, may be causally involved in depression. Because norepinephrine transmission itself can have antidepressant properties, it is likely that a different LC-derived neuromodulator is responsible. Galanin is a neuropeptide that is enriched in LC neurons and has pro-depressant effects. Therefore, the overarching hypothesis for this project is that LC hyperactivity and resulting galanin transmission can cause depression-like behavior. The proposed project will combine optogenetic and in vivo electrophysiology techniques to modulate and measure neuron activity with genetic approaches to manipulate galanin in behavioral assays of depression-like behavior in mice. In Aim 1, I will use optogenetics to determine whether driving LC firing frequencies that cause galanin release can induce depressive-like behavior in wild-type or genetically altered mice with overexpression or depletion of LC-derived galanin. In Aim 2, I will assess the ability of optogenetically-induced LC hyperactivity to alter the activity of ventral tegmental area (VTA) dopaminergic neurons, which are thought to be compromised in depression-related behaviors, and determine the contribution of galanin using the genetically altered mice described above. These experiments will be the first to precisely test the causal relationship between LC hyperactivity and depression and determine the contribution of LC-derived galanin and suppression of VTA dopamine neurons, which will help pave the way for the development of effective, targeted therapeutics to treat people with depression.
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