Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives

Schizophrenia is recognized to be a highly heterogeneous disease at various levels, from genetics to clinical manifestations and treatment sensitivity. This heterogeneity is also reflected in the variety of oxidative stress-related mechanisms contributing to the phenotypic realization and manifestat...

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Main Authors: Evgeny A. Ermakov, Elena M. Dmitrieva, Daria A. Parshukova, Daria V. Kazantseva, Alisa R. Vasilieva, Liudmila P. Smirnova
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:Oxidative Medicine and Cellular Longevity
Online Access:http://dx.doi.org/10.1155/2021/8881770
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spelling doaj-aedacebc9d7442c785f297af78911f0e2021-02-15T12:53:11ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942021-01-01202110.1155/2021/88817708881770Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment PerspectivesEvgeny A. Ermakov0Elena M. Dmitrieva1Daria A. Parshukova2Daria V. Kazantseva3Alisa R. Vasilieva4Liudmila P. Smirnova5Laboratory of Repair Enzymes, Institute of Chemical Biology and Fundamental Medicine, Siberian Division of Russian Academy of Sciences, Novosibirsk 630090, RussiaLaboratory of Molecular Genetics and Biochemistry, Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk 634014, RussiaLaboratory of Molecular Genetics and Biochemistry, Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk 634014, RussiaSiberian State Medical University, Tomsk 634055, RussiaSiberian State Medical University, Tomsk 634055, RussiaLaboratory of Molecular Genetics and Biochemistry, Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk 634014, RussiaSchizophrenia is recognized to be a highly heterogeneous disease at various levels, from genetics to clinical manifestations and treatment sensitivity. This heterogeneity is also reflected in the variety of oxidative stress-related mechanisms contributing to the phenotypic realization and manifestation of schizophrenia. At the molecular level, these mechanisms are supposed to include genetic causes that increase the susceptibility of individuals to oxidative stress and lead to gene expression dysregulation caused by abnormal regulation of redox-sensitive transcriptional factors, noncoding RNAs, and epigenetic mechanisms favored by environmental insults. These changes form the basis of the prooxidant state and lead to altered redox signaling related to glutathione deficiency and impaired expression and function of redox-sensitive transcriptional factors (Nrf2, NF-κB, FoxO, etc.). At the cellular level, these changes lead to mitochondrial dysfunction and metabolic abnormalities that contribute to aberrant neuronal development, abnormal myelination, neurotransmitter anomalies, and dysfunction of parvalbumin-positive interneurons. Immune dysfunction also contributes to redox imbalance. At the whole-organism level, all these mechanisms ultimately contribute to the manifestation and development of schizophrenia. In this review, we consider oxidative stress-related mechanisms and new treatment perspectives associated with the correction of redox imbalance in schizophrenia. We suggest that not only antioxidants but also redox-regulated transcription factor-targeting drugs (including Nrf2 and FoxO activators or NF-κB inhibitors) have great promise in schizophrenia. But it is necessary to develop the stratification criteria of schizophrenia patients based on oxidative stress-related markers for the administration of redox-correcting treatment.http://dx.doi.org/10.1155/2021/8881770
collection DOAJ
language English
format Article
sources DOAJ
author Evgeny A. Ermakov
Elena M. Dmitrieva
Daria A. Parshukova
Daria V. Kazantseva
Alisa R. Vasilieva
Liudmila P. Smirnova
spellingShingle Evgeny A. Ermakov
Elena M. Dmitrieva
Daria A. Parshukova
Daria V. Kazantseva
Alisa R. Vasilieva
Liudmila P. Smirnova
Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
Oxidative Medicine and Cellular Longevity
author_facet Evgeny A. Ermakov
Elena M. Dmitrieva
Daria A. Parshukova
Daria V. Kazantseva
Alisa R. Vasilieva
Liudmila P. Smirnova
author_sort Evgeny A. Ermakov
title Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
title_short Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
title_full Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
title_fullStr Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
title_full_unstemmed Oxidative Stress-Related Mechanisms in Schizophrenia Pathogenesis and New Treatment Perspectives
title_sort oxidative stress-related mechanisms in schizophrenia pathogenesis and new treatment perspectives
publisher Hindawi Limited
series Oxidative Medicine and Cellular Longevity
issn 1942-0900
1942-0994
publishDate 2021-01-01
description Schizophrenia is recognized to be a highly heterogeneous disease at various levels, from genetics to clinical manifestations and treatment sensitivity. This heterogeneity is also reflected in the variety of oxidative stress-related mechanisms contributing to the phenotypic realization and manifestation of schizophrenia. At the molecular level, these mechanisms are supposed to include genetic causes that increase the susceptibility of individuals to oxidative stress and lead to gene expression dysregulation caused by abnormal regulation of redox-sensitive transcriptional factors, noncoding RNAs, and epigenetic mechanisms favored by environmental insults. These changes form the basis of the prooxidant state and lead to altered redox signaling related to glutathione deficiency and impaired expression and function of redox-sensitive transcriptional factors (Nrf2, NF-κB, FoxO, etc.). At the cellular level, these changes lead to mitochondrial dysfunction and metabolic abnormalities that contribute to aberrant neuronal development, abnormal myelination, neurotransmitter anomalies, and dysfunction of parvalbumin-positive interneurons. Immune dysfunction also contributes to redox imbalance. At the whole-organism level, all these mechanisms ultimately contribute to the manifestation and development of schizophrenia. In this review, we consider oxidative stress-related mechanisms and new treatment perspectives associated with the correction of redox imbalance in schizophrenia. We suggest that not only antioxidants but also redox-regulated transcription factor-targeting drugs (including Nrf2 and FoxO activators or NF-κB inhibitors) have great promise in schizophrenia. But it is necessary to develop the stratification criteria of schizophrenia patients based on oxidative stress-related markers for the administration of redox-correcting treatment.
url http://dx.doi.org/10.1155/2021/8881770
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