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PMID: 2185538 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Dopaminergic mechanisms in idiopathic and drug-induced psychoses.

Schizophrenia bulletin ·Vol. 16 ·No. 1 ·1990-00-00 ·Pages 97-110

Lieberman JA, Kinon BJ, Loebel AD

Abstract

Stimulant drugs such as cocaine and amphetamine are among the most commonly abused substances by schizophrenic patients. This may be due in part to aspects of the illness and treatment side effects that impel patients to use dopamine agonist drugs. Dopaminergic neural systems have been shown to mediate both stimulant drug effects and schizophrenia. Because of the hypothesized overlap in the pathophysiology of schizophrenia and the neurobiological effects of chronic stimulant use, the potential for serious complication of the primary disease by substance abuse exists. This article reviews the neurobiological mechanisms of behavioral sensitization and neurotoxicity associated with chronic stimulant administration in the context of pathophysiological theories of schizophrenia. Discussion focuses on the potential impact of stimulant use on the disease process as well as the manifest phenomenology and course of schizophrenia.

MeSH Terms
Amphetamine/adverse effects Animals Brain/drug effects Cocaine/adverse effects Dopamine/physiology Dose-Response Relationship, Drug Humans Psychoses, Substance-Induced/physiopathology Receptors, Dopamine/drug effects Schizophrenia/physiopathology Schizophrenic Psychology Substance-Related Disorders/physiopathology
Chemicals
Receptors, Dopamine Amphetamine Cocaine Dopamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lieberman J A
Hillside Hospital, Glen Oaks, NY 11004.
Kinon B J
Loebel A D
Article Info
Journal
Schizophrenia bulletin
Abbr.
Schizophr Bull
ISSN
0586-7614
Published
1990-00-00
Pages
97-110
Language
English
Region
United States
NLM ID
0236760
Subset
IM
Grants
NIMH NIH HHS · MH-00537 · United States
NIMH NIH HHS · MH-41646 · United States
NIMH NIH HHS · MH-41960 · United States
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