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Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits

Negative symptoms of schizophrenia are debilitating and chronic in nature, are difficult to treat, and contribute to poor functional outcomes. Motivational deficits are a core negative symptom and may involve alterations in reward processing, which involve subcortical regions such as the basal gangl...

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Autores principales: Goldsmith, David R., Rapaport, Mark Hyman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044128/
https://www.ncbi.nlm.nih.gov/pubmed/32153436
http://dx.doi.org/10.3389/fpsyt.2020.00046
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author Goldsmith, David R.
Rapaport, Mark Hyman
author_facet Goldsmith, David R.
Rapaport, Mark Hyman
author_sort Goldsmith, David R.
collection PubMed
description Negative symptoms of schizophrenia are debilitating and chronic in nature, are difficult to treat, and contribute to poor functional outcomes. Motivational deficits are a core negative symptom and may involve alterations in reward processing, which involve subcortical regions such as the basal ganglia. More specifically, dopamine-rich regions like the ventral striatum, have been implicated in these reward-processing deficits. Inflammation is one mechanism that may underlie negative symptoms, and specifically motivational deficits, via the effects of inflammatory cytokines on the basal ganglia. Previous work has demonstrated that inflammatory stimuli decrease neural activity in the ventral striatum and decrease connectivity in reward-relevant neural circuitry. The immune system has been shown to be involved in the pathophysiology of schizophrenia, and inflammatory cytokines have been shown to be altered in patients with the disorder. This paper reviews the literature on associations between inflammatory markers and negative symptoms of schizophrenia as well as the role of anti-inflammatory drugs to target negative symptoms. We also review the literature on the role of inflammation and reward processing deficits in both healthy controls and individuals with depression. We use the literature on inflammation and depression as a basis for a model that explores potential mechanisms responsible for inflammation modulating certain aspects of negative symptoms in patients with schizophrenia. This approach may offer novel targets to treat these symptoms of the disorder that are significant barriers to functional recovery and do not respond well to available antipsychotic medications.
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spelling pubmed-70441282020-03-09 Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits Goldsmith, David R. Rapaport, Mark Hyman Front Psychiatry Psychiatry Negative symptoms of schizophrenia are debilitating and chronic in nature, are difficult to treat, and contribute to poor functional outcomes. Motivational deficits are a core negative symptom and may involve alterations in reward processing, which involve subcortical regions such as the basal ganglia. More specifically, dopamine-rich regions like the ventral striatum, have been implicated in these reward-processing deficits. Inflammation is one mechanism that may underlie negative symptoms, and specifically motivational deficits, via the effects of inflammatory cytokines on the basal ganglia. Previous work has demonstrated that inflammatory stimuli decrease neural activity in the ventral striatum and decrease connectivity in reward-relevant neural circuitry. The immune system has been shown to be involved in the pathophysiology of schizophrenia, and inflammatory cytokines have been shown to be altered in patients with the disorder. This paper reviews the literature on associations between inflammatory markers and negative symptoms of schizophrenia as well as the role of anti-inflammatory drugs to target negative symptoms. We also review the literature on the role of inflammation and reward processing deficits in both healthy controls and individuals with depression. We use the literature on inflammation and depression as a basis for a model that explores potential mechanisms responsible for inflammation modulating certain aspects of negative symptoms in patients with schizophrenia. This approach may offer novel targets to treat these symptoms of the disorder that are significant barriers to functional recovery and do not respond well to available antipsychotic medications. Frontiers Media S.A. 2020-02-20 /pmc/articles/PMC7044128/ /pubmed/32153436 http://dx.doi.org/10.3389/fpsyt.2020.00046 Text en Copyright © 2020 Goldsmith and Rapaport http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Goldsmith, David R.
Rapaport, Mark Hyman
Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title_full Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title_fullStr Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title_full_unstemmed Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title_short Inflammation and Negative Symptoms of Schizophrenia: Implications for Reward Processing and Motivational Deficits
title_sort inflammation and negative symptoms of schizophrenia: implications for reward processing and motivational deficits
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044128/
https://www.ncbi.nlm.nih.gov/pubmed/32153436
http://dx.doi.org/10.3389/fpsyt.2020.00046
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