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DOPAMINE IN SCHIZOPHRENIA - A REVIEW AND RECONCEPTUALIZATION
Author(s): DAVIS KL, KAHN RS, KO G, DAVIDSON M
Source: AMERICAN JOURNAL OF PSYCHIATRY    Volume: 148    Issue: 11    Pages: 1474-1486    Published: NOV 1991  
Times Cited: 794     References: 132     
Abstract: Objective: The initial hypothesis that schizophrenia is a manifestation of hyperdopaminergia has recently been faulted. However, several new findings suggest that abnormal, although not necessarily excessive, dopamine activity is an important factor in schizophrenia. The authors discuss these findings and their implications. Method: All published studies regarding dopamine and schizophrenia and all studies on the role of dopamine in cognition were reviewed. Attention has focused on post-mortem studies, positron emission tomography, neuroleptic drug actions, plasma levels of the dopamine metabolite homovanillic acid (HVA), and cerebral blood flow. Results: Evidence, particularly from intracellular recording studies in animals and plasma HVA measurements, suggests that neuroleptics act by reducing dopamine activity in mesolimbic dopamine neurons. Post-mortem studies have shown high dopamine and HVA concentrations in various subcortical brain regions and greater than normal dopamine receptor densities in the brains of schizophrenic patients. On the other hand, the negative/deficit symptom complex of schizophrenia may be associated with low dopamine activity in the prefrontal cortex. Recent animal and human studies suggest that prefrontal dopamine neurons inhibit subcortical dopamine activity. The authors hypothesize that schizophrenia is characterized by abnormally low prefrontal dopamine activity (causing deficit symptoms) leading to excessive dopamine activity in mesolimbic dopamine neurons (causing positive symptoms). Conclusions: The possible co-occurrence of high and low dopamine activity in schizophrenia has implications for the conceptualization of dopamine's role in schizophrenia. It would explain the concurrent presence of negative and positive symptoms. This hypothesis is testable and has important implications for treatment of schizophrenia and schizophrenia spectrum disorders.
Document Type: Review
Language: English
Reprint Address: DAVIS, KL (reprint author), MT SINAI HOSP, DEPT PSYCHIAT, BOX 1230, 1 GUSTAVE L LEVY PL, NEW YORK, NY 10029 USA
Publisher: AMER PSYCHIATRIC ASSOCIATION, 1400 K ST NW, WASHINGTON, DC 20005
Subject Category: Psychiatry
IDS Number: GM202
ISSN: 0002-953X
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