The thrust of this neuroscience research center proposal will be to elucidate neurobiological components of schizophrenia. The research center involves both clinical and preclinical investigations delineating neurobiological brain abnormalities in schizophrenia and the actions of psychotic drugs. Through the use of this center research scientists will collaborate to study these problems at the anatomical, immunocytochemical molecular neurobiological, biochemical, neurophysiological, clinical and behavior levels. Two general themes will be investigated: 1) brain abnormalities in adult schizophrenic patients and fetuses at high risk for schizophrenia and 2) phencyclidine (PCP) as a model for schizophrenia and the design of investigations around this model. The first line of research involves an anatomical survey of potential forebrain pathology comparing anatomical and immunocytochemical features of targeted areas of the brain. The second PCP research area involves the study of the PCP NMDA receptor complex in high risk fetal and adult schizophrenic brains as compared to controls, PET studies of patients abusing PCP, development of a ligand for the PCP and NMDA site in man, the study of alpha endopsychosin in high risk fetal and adult schizophrenic brains and the investigation of CSF in schizophrenic patients. Alterations in dopamine is a current theory of neurotransmitter pathology in schizophrenia. D1 and D2 receptors will be studied in animals and high risk fetal and adult schizophrenic brains along with their interaction with excitatory amino acids. Novel treatment strategies for PCP psychosis are suggested.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH044188-02
Application #
3107283
Study Section
Special Emphasis Panel (SRCM (06))
Project Start
1989-03-01
Project End
1994-02-28
Budget Start
1990-03-01
Budget End
1991-02-28
Support Year
2
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Albert, Katherine A; Hemmings Jr, Hugh C; Adamo, Anna I B et al. (2002) Evidence for decreased DARPP-32 in the prefrontal cortex of patients with schizophrenia. Arch Gen Psychiatry 59:705-12
Bunney Jr, W E; Hetrick, W P; Bunney, B G et al. (1999) Structured Interview for Assessing Perceptual Anomalies (SIAPA). Schizophr Bull 25:577-92
Jin, Y; Bunney Jr, W E; Sandman, C A et al. (1998) Is P50 suppression a measure of sensory gating in schizophrenia? Biol Psychiatry 43:873-8
Jones, E G (1997) Cortical development and thalamic pathology in schizophrenia. Schizophr Bull 23:483-501
Jin, Y; Potkin, S G; Patterson, J V et al. (1997) Effects of P50 temporal variability on sensory gating in schizophrenia. Psychiatry Res 70:71-81
Katz, M; Buchsbaum, M S; Siegel Jr, B V et al. (1996) Correlational patterns of cerebral glucose metabolism in never-medicated schizophrenics. Neuropsychobiology 33:1-11
Hetrick, W P; Sandman, C A; Bunney Jr, W E et al. (1996) Gender differences in gating of the auditory evoked potential in normal subjects. Biol Psychiatry 39:51-8
Akbarian, S; Sucher, N J; Bradley, D et al. (1996) Selective alterations in gene expression for NMDA receptor subunits in prefrontal cortex of schizophrenics. J Neurosci 16:19-30
Schroder, J; Buchsbaum, M S; Siegel, B V et al. (1996) Cerebral metabolic activity correlates of subsyndromes in chronic schizophrenia. Schizophr Res 19:41-53
Buchsbaum, M S; Someya, T; Teng, C Y et al. (1996) PET and MRI of the thalamus in never-medicated patients with schizophrenia. Am J Psychiatry 153:191-9

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