At the request of NIMH (Division of Neuroscience and Basic Behavioral Science, Dr. Douglas Meinecke), this Supplemental application corresponds to Funded Years 03 and 04 of """"""""Hippocampal Atrophy in Major Depression (RO1 MH 67996; PI: C. Stockmeier). The request for Supplemental support to continue and expand tissue collection is an extension of Supplemental Postmortem Brain Collection funding (NOT-MH-01- 010) awarded to Dr. Gregory Ordway as part of RO1 63187 (06/01/02 -11/30/05), and 11 years of NIMH funding for collection to the PI prior to that. Neuroimaging and postmortem brain studies provide evidence for hippocampal pathology in major depressive disorder (MDD). It is hypothesized that a decrease in hippocampal neuropil, in response to diminished markers of neural growth and synaptic connection, resulting in an increase in neuronal and glial density, is the microscopic basis for the histopathology of the hippocampus in MDD. To meet the Specific Aims of the parent RO1 (MH 67996), supplemental funds are requested for the collection of 1) human brain tissue at autopsy and 2) sufficient clinical information from next-of-kin and medical records for retrospective assessment of DSM-IV psychiatric disorders. With informed written consent, brain tissue is sought from subjects suffering a major depressive episode in the last two weeks of life and psychiatrically-normal control subjects matched for age, gender, postmortem interval arid tissue pH. These depressed subjects will not be receiving antidepressant or antipsychotic treatment at the time of death and all subjects must be neurologically and neuropathologically normal. Subjects with MDD must have no current co-morbid Axis I diagnosis of an alcohol or psychoactive substance use disorder. The presence or absence of MDD is determined by consensus diagnosis based on medical records and data gathered from next-of-kin of all subjects with the Structured Clinical Interview for DSM IV Psychiatric Disorders (SCID). At current collection rates, the collection of 6-8 subjects with MDD and about 10 normal control subjects per year for the next two years will permit achievement of the funded specific aims. Current NIH funding to Drs.C. Stockmeier, G. Ordway, G. Rajkowska, R. Duman, B. Karolewicz and M. Austin depends solely on this Supplement for brain tissue to better understanding of the cellular and molecular pathophysiology of the major mental illnesses. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
3R01MH067996-03S1
Application #
7026827
Study Section
Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section (NPAS)
Program Officer
Meinecke, Douglas L
Project Start
2003-03-01
Project End
2007-11-30
Budget Start
2006-01-20
Budget End
2006-11-30
Support Year
3
Fiscal Year
2006
Total Cost
$198,362
Indirect Cost
Name
University of Mississippi Medical Center
Department
Psychiatry
Type
Schools of Medicine
DUNS #
928824473
City
Jackson
State
MS
Country
United States
Zip Code
39216
Athey, Alison; Overholser, James; Bagge, Courtney et al. (2018) Risk-taking behaviors and stressors differentially predict suicidal preparation, non-fatal suicide attempts, and suicide deaths. Psychiatry Res 270:160-167
Mahajan, Gouri J; Vallender, Eric J; Garrett, Michael R et al. (2018) Altered neuro-inflammatory gene expression in hippocampus in major depressive disorder. Prog Neuropsychopharmacol Biol Psychiatry 82:177-186
Cobb, J A; O'Neill, K; Milner, J et al. (2016) Density of GFAP-immunoreactive astrocytes is decreased in left hippocampi in major depressive disorder. Neuroscience 316:209-20
Rubinow, Marisa J; Mahajan, Gouri; May, Warren et al. (2016) Basolateral amygdala volume and cell numbers in major depressive disorder: a postmortem stereological study. Brain Struct Funct 221:171-84
Rafalo-Ulinska, Anna; Piotrowska, Joanna; Kryczyk, Agata et al. (2016) Zinc transporters protein level in postmortem brain of depressed subjects and suicide victims. J Psychiatr Res 83:220-229
Harris, Sharonda; Johnson, Shakevia; Duncan, Jeremy W et al. (2015) Evidence revealing deregulation of the KLF11-MAO A pathway in association with chronic stress and depressive disorders. Neuropsychopharmacology 40:1373-82
Fisher, Lauren B; Overholser, James C; Dieter, Lesa (2015) Methods of committing suicide among 2,347 people in Ohio. Death Stud 39:39-43
Johnson, Shakevia; Duncan, Jeremy; Hussain, Syed A et al. (2015) The IFN?-PKR pathway in the prefrontal cortex reactions to chronic excessive alcohol use. Alcohol Clin Exp Res 39:476-84
Gomez-Sanchez, Elise P (2015) Salt-sensitive hypertension: food for thought. Hypertension 65:283-4
Gomez-Sanchez, Elise; Gomez-Sanchez, Celso E (2014) The multifaceted mineralocorticoid receptor. Compr Physiol 4:965-94

Showing the most recent 10 out of 44 publications