The proposed research continues previously funded studies on the pathophysiology of psychotic major depression (PMD), a severe and often debilitating form of depression. Results thus far indicate that PMD patients have increased and phase advanced corticotropin (ACTH) circadian rhythms, increased overnight cortisol levels, and prefrontal cognitive deficits that may originate in glucocorticoid (GC) effects on ascending mesocortical dopamine (DA) pathways. Parallel studies in animals indicate that chronic administration of GC's decreases DA utilization in rat prefrontal cortex, and impairs prefrontal DA mediated cognitive performance in squirrel monkeys. Moreover, GC receptor blockade by mifepristone produces rapid relief of PMD cognitive impairments as measured by psychiatric tests. Based on these results, the proposed studies test the following four hypotheses: (l) Hypothalamic-pituitary-adrenal (HPA) axis dysregulation in PMD is associated with specific cognitive impairments in executive functions, attention, and semantic analysis, and with correlated volumetric losses and functional activation abnormalities in prefrontal cortex and the hippocampal formation, as measured by structural and functional magnetic resonance imaging (fMRI); (2) Mifepristone treatment relieves PMD cognitive deficits and delusional symptoms as measured by psychometric and psychiatric tests, normalizes the PMD phase advance in plasma ACTH circadian rhythms, and is accompanied by functional reorganizations in prefrontal cortical networks as measured by fMRI; (3) In monkeys, chronic stress induces prefrontal cognitive impairments analogous to those seen previously with chronic UC treatment, and these stress effects are blocked by mifepristone; and (4) In rats, mifepristone blocks the effects of chronic stress and chronic GC treatment on prefrontal DA metabolism. The approaches used to address these aims move across the boundaries of clinical psychopharmacology, basic behavioral neuroscience, experimental neurochemistry, and functional neuroimaging, with the ultimate goal of understanding why some depressed patients become psychotic or otherwise cognitively impaired, and uncovering new and faster methods of treatment for PMD and related psychotic disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
2R01MH050604-05
Application #
2901726
Study Section
Special Emphasis Panel (ZRG1-BDCN-6 (01))
Program Officer
Meinecke, Douglas L
Project Start
1994-09-01
Project End
2004-05-31
Budget Start
1999-09-01
Budget End
2000-05-31
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Davis, Elena Goetz; Keller, Jennifer; Hallmayer, Joachim et al. (2018) Corticotropin-releasing factor 1 receptor haplotype and cognitive features of major depression. Transl Psychiatry 8:5
Keller, J; Gomez, R; Williams, G et al. (2017) HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition. Mol Psychiatry 22:527-536
Schatzberg, A F; Keller, J; Tennakoon, L et al. (2014) HPA axis genetic variation, cortisol and psychosis in major depression. Mol Psychiatry 19:220-7
Cohen, Jeremy D; Nichols, Taylor; Keller, Jennifer et al. (2013) Insular cortex abnormalities in psychotic major depression: relationship to gender and psychotic symptoms. Neurosci Res 75:331-9
Lembke, Anna; Gomez, Rowena; Tenakoon, Lakshika et al. (2013) The mineralocorticoid receptor agonist, fludrocortisone, differentially inhibits pituitary-adrenal activity in humans with psychotic major depression. Psychoneuroendocrinology 38:115-21
Kelley, Ryan; Garrett, Amy; Cohen, Jeremy et al. (2013) Altered brain function underlying verbal memory encoding and retrieval in psychotic major depression. Psychiatry Res 211:119-26
Etkin, Amit; Schatzberg, Alan F (2011) Common abnormalities and disorder-specific compensation during implicit regulation of emotional processing in generalized anxiety and major depressive disorders. Am J Psychiatry 168:968-78
Greicius, Michael D; Flores, Benjamin H; Menon, Vinod et al. (2007) Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biol Psychiatry 62:429-37
Parker, Karen J; Rainwater, Kimberly L; Buckmaster, Christine L et al. (2007) Early life stress and novelty seeking behavior in adolescent monkeys. Psychoneuroendocrinology 32:785-92
Lyons, David M; Parker, Karen J; Zeitzer, Jamie M et al. (2007) Preliminary evidence that hippocampal volumes in monkeys predict stress levels of adrenocorticotropic hormone. Biol Psychiatry 62:1171-4

Showing the most recent 10 out of 15 publications