Over the past seven years, scientists at the University of Pittsburgh and Carnegie Mellon University have work together investigating the pathophysiology of schizophrenia. We have acquired substantial experience in the organization and operation of a translational center focused at the interface of basic and clinical neuroscience, and we have established a milieu in which basic and clinical neuroscientists collaborative productively on multidisciplinary issues. Our plans for this renewal application represent not only the logical extension of the ongoing research activities of individual projects in our Center, but also include the synergistic research programs that have resulted from interactions among Center investigators. Consequently, this application contains descriptions of eight integrated research projects, supported by four cores. Through this program of research, we are attempting to test complementary aspects of the following central hypothesis: Certain cognitive abnormalities characteristic of schizophrenia are due to an impairment of functions dependent on the dorsolateral prefrontal cortex (DLPFC). These dysfunctions arise during development as a consequence of interrelated abnormalities in specific subsets of the glutamate, GABA and dopamine components of the DLPFC circuitry. This abnormalities lead to altered glutamateric output from the DLPFC to cortical association regions, mediodorsal thalamic nucleus and nucleus accumbens. This hypothesis guides the work conducted within each project, and is subject to modification by the results obtained from each project. As a result of our extensive interactions, all Center investigators are made are of the data that suggest modifications to the hypothesis, and they are then able to make appropriate adjustments in their study designs or experimental models. Thus,our objective is to operate in a truly bidirectional fashion such that individual projects both attend to and contribute to the central hypothesis. In addition, our plans reflect the continuing evolution of our Center as they incorporate novel research opportunities that have developed in association with the integration of new faculty into the Center, including senior scientists who recruitment to Pittsburgh was in part facilitated by our CNMD, as well as junior faculty whose research careers have developed within the context of our Center.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH045156-10
Application #
2890407
Study Section
Special Emphasis Panel (ZMH1-NRB-R (02))
Program Officer
Huerta, Michael F
Project Start
1990-04-01
Project End
2003-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
10
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Psychiatry
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Cai, HuaLin; Zhou, Xiang; Dougherty, George G et al. (2018) Pregnenolone-progesterone-allopregnanolone pathway as a potential therapeutic target in first-episode antipsychotic-naïve patients with schizophrenia. Psychoneuroendocrinology 90:43-51
Stevenson, J M; Reilly, J L; Harris, M S H et al. (2016) Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes. Transl Psychiatry 6:e739
Lizano, Paulo L; Keshavan, Matcheri S; Tandon, Neeraj et al. (2016) Angiogenic and immune signatures in plasma of young relatives at familial high-risk for psychosis and first-episode patients: A preliminary study. Schizophr Res 170:115-22
Horton, Leslie E; Tarbox, Sarah I; Olino, Thomas M et al. (2015) Trajectories of premorbid childhood and adolescent functioning in schizophrenia-spectrum psychoses: A first-episode study. Psychiatry Res 227:339-46
Bishop, Jeffrey R; Reilly, James L; Harris, Margret S H et al. (2015) Pharmacogenetic associations of the type-3 metabotropic glutamate receptor (GRM3) gene with working memory and clinical symptom response to antipsychotics in first-episode schizophrenia. Psychopharmacology (Berl) 232:145-54
Hall, Nathan; Colby, Carol (2014) S-cone visual stimuli activate superior colliculus neurons in old world monkeys: implications for understanding blindsight. J Cogn Neurosci 26:1234-56
Subramanian, Janani; Colby, Carol L (2014) Shape selectivity and remapping in dorsal stream visual area LIP. J Neurophysiol 111:613-27
Berdyyeva, Tamara K; Olson, Carl R (2014) Intracortical microstimulation of supplementary eye field impairs ability of monkeys to make serially ordered saccades. J Neurophysiol 111:1529-40
Lencer, Rebekka; Bishop, Jeffrey R; Harris, Margret S H et al. (2014) Association of variants in DRD2 and GRM3 with motor and cognitive function in first-episode psychosis. Eur Arch Psychiatry Clin Neurosci 264:345-55
Richard, Annette E; Carter, Cameron S; Cohen, Jonathan D et al. (2013) Persistence, diagnostic specificity and genetic liability for context-processing deficits in schizophrenia. Schizophr Res 147:75-80

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