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Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients

BACKGROUND: The aim of this study was to determine glutathione levels and antioxidant enzyme activities in the drug-naive first-episode patients with schizophrenia in comparison with healthy control subjects. METHODS: It was a case-controlled study carried on twenty-three patients (20 men and 3 wome...

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Autores principales: Raffa, Monia, Atig, Fatma, Mhalla, Ahmed, Kerkeni, Abdelhamid, Mechri, Anwar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161936/
https://www.ncbi.nlm.nih.gov/pubmed/21810251
http://dx.doi.org/10.1186/1471-244X-11-124
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author Raffa, Monia
Atig, Fatma
Mhalla, Ahmed
Kerkeni, Abdelhamid
Mechri, Anwar
author_facet Raffa, Monia
Atig, Fatma
Mhalla, Ahmed
Kerkeni, Abdelhamid
Mechri, Anwar
author_sort Raffa, Monia
collection PubMed
description BACKGROUND: The aim of this study was to determine glutathione levels and antioxidant enzyme activities in the drug-naive first-episode patients with schizophrenia in comparison with healthy control subjects. METHODS: It was a case-controlled study carried on twenty-three patients (20 men and 3 women, mean age = 29.3 ± 7.5 years) recruited in their first-episode of schizophrenia and 40 healthy control subjects (36 men and 9 women, mean age = 29.6 ± 6.2 years). In patients, the blood samples were obtained prior to the initiation of neuroleptic treatments. Glutathione levels: total glutathione (GSHt), reduced glutathione (GSHr) and oxidized glutathione (GSSG) and antioxidant enzyme activities: superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT) were determined by spectrophotometry. RESULTS: GSHt and reduced GSHr were significantly lower in patients than in controls, whereas GSSG was significantly higher in patients. GPx activity was significantly higher in patients compared to control subjects. CAT activity was significantly lower in patients, whereas the SOD activity was comparable to that of controls. CONCLUSION: This is a report of decreased plasma levels of GSHt and GSHr, and impaired antioxidant enzyme activities in drug-naive first-episode patients with schizophrenia. The GSH deficit seems to be implicated in psychosis, and may be an important indirect biomarker of oxidative stress in schizophrenia early in the course of illness. Finally, our results provide support for further studies of the possible role of antioxidants as neuroprotective therapeutic strategies for schizophrenia from early stages.
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spelling pubmed-31619362011-08-26 Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients Raffa, Monia Atig, Fatma Mhalla, Ahmed Kerkeni, Abdelhamid Mechri, Anwar BMC Psychiatry Research Article BACKGROUND: The aim of this study was to determine glutathione levels and antioxidant enzyme activities in the drug-naive first-episode patients with schizophrenia in comparison with healthy control subjects. METHODS: It was a case-controlled study carried on twenty-three patients (20 men and 3 women, mean age = 29.3 ± 7.5 years) recruited in their first-episode of schizophrenia and 40 healthy control subjects (36 men and 9 women, mean age = 29.6 ± 6.2 years). In patients, the blood samples were obtained prior to the initiation of neuroleptic treatments. Glutathione levels: total glutathione (GSHt), reduced glutathione (GSHr) and oxidized glutathione (GSSG) and antioxidant enzyme activities: superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT) were determined by spectrophotometry. RESULTS: GSHt and reduced GSHr were significantly lower in patients than in controls, whereas GSSG was significantly higher in patients. GPx activity was significantly higher in patients compared to control subjects. CAT activity was significantly lower in patients, whereas the SOD activity was comparable to that of controls. CONCLUSION: This is a report of decreased plasma levels of GSHt and GSHr, and impaired antioxidant enzyme activities in drug-naive first-episode patients with schizophrenia. The GSH deficit seems to be implicated in psychosis, and may be an important indirect biomarker of oxidative stress in schizophrenia early in the course of illness. Finally, our results provide support for further studies of the possible role of antioxidants as neuroprotective therapeutic strategies for schizophrenia from early stages. BioMed Central 2011-08-02 /pmc/articles/PMC3161936/ /pubmed/21810251 http://dx.doi.org/10.1186/1471-244X-11-124 Text en Copyright ©2011 Raffa et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Raffa, Monia
Atig, Fatma
Mhalla, Ahmed
Kerkeni, Abdelhamid
Mechri, Anwar
Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title_full Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title_fullStr Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title_full_unstemmed Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title_short Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
title_sort decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161936/
https://www.ncbi.nlm.nih.gov/pubmed/21810251
http://dx.doi.org/10.1186/1471-244X-11-124
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