Abstract
Chronic prescription of antipsychotics seems to lose its therapeutic benefits in the prevention of recurring psychotic symptoms. In many instances, the occurrence of relapse from initial remission is followed by an increase in dose of the prescribed antipsychotic. The current understanding of why this occurs is still in its infancy, but a controversial idea that has regained attention recently is the notion of iatrogenic dopamine supersensitivity. Studies on cell cultures and animal models have shown that long-term antipsychotic use is linked to both an upregulation of dopamine D2-receptors in the striatum and the emergence of enhanced receptor affinity to endogenous dopamine. These findings have been hypothesized to contribute to the phenomenon known as dopamine supersensitivity psychosis (DSP), which has been clinically typified as the foundation of rebound psychosis, drug tolerance, and tardive dyskinesia. The focus of this review is the update of evidence behind the classification of antipsychotic induced DSP and an investigation of its relationship to treatment resistance. Since antipsychotics are the foundation of illness management, a greater understanding of DSP and its prevention may greatly affect patient outcomes.
Keywords: Antipsychotics, dopamine supersensitivity psychosis, D2-receptors, rebound psychosis, relapse, schizophrenia, treatment-resistance, tolerance.
Current Neuropharmacology
Title:Antipsychotic Induced Dopamine Supersensitivity Psychosis: A Comprehensive Review
Volume: 15 Issue: 1
Author(s): John Yin, Alasdair M. Barr, Alfredo Ramos-Miguel and Ric M. Procyshyn
Affiliation:
Keywords: Antipsychotics, dopamine supersensitivity psychosis, D2-receptors, rebound psychosis, relapse, schizophrenia, treatment-resistance, tolerance.
Abstract: Chronic prescription of antipsychotics seems to lose its therapeutic benefits in the prevention of recurring psychotic symptoms. In many instances, the occurrence of relapse from initial remission is followed by an increase in dose of the prescribed antipsychotic. The current understanding of why this occurs is still in its infancy, but a controversial idea that has regained attention recently is the notion of iatrogenic dopamine supersensitivity. Studies on cell cultures and animal models have shown that long-term antipsychotic use is linked to both an upregulation of dopamine D2-receptors in the striatum and the emergence of enhanced receptor affinity to endogenous dopamine. These findings have been hypothesized to contribute to the phenomenon known as dopamine supersensitivity psychosis (DSP), which has been clinically typified as the foundation of rebound psychosis, drug tolerance, and tardive dyskinesia. The focus of this review is the update of evidence behind the classification of antipsychotic induced DSP and an investigation of its relationship to treatment resistance. Since antipsychotics are the foundation of illness management, a greater understanding of DSP and its prevention may greatly affect patient outcomes.
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Cite this article as:
Yin John, Barr M. Alasdair, Ramos-Miguel Alfredo and Procyshyn M. Ric, Antipsychotic Induced Dopamine Supersensitivity Psychosis: A Comprehensive Review, Current Neuropharmacology 2017; 15 (1) . https://dx.doi.org/10.2174/1570159X14666160606093602
DOI https://dx.doi.org/10.2174/1570159X14666160606093602 |
Print ISSN 1570-159X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6190 |
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