Abstract

Altered antioxidant status has been reported in schizophrenia. The glutathione (GSH) redox system is important for reducing oxidative stress. GSH, a radical scavenger, is converted to oxidized glutathione (GSSG) through glutathione peroxidase (GPx), and converted back to GSH by glutathione reductase (GR). Measurements of GSH, GSSG and its related enzymatic reactions are thus important for evaluating the redox and antioxidant status. In the present study, levels of GSH, GSSG, GPx and GR were assessed in the caudate region of postmortem brains from schizophrenic patients and control subjects (with and without other psychiatric disorders). Significantly lower levels of GSH, GPx, and GR were found in schizophrenic group than in control groups without any psychiatric disorders. Concomitantly, a decreased GSH:GSSG ratio was also found in schizophrenic group. Moreover, both GSSG and GR levels were significantly and inversely correlated to age of schizophrenic patients, but not control subjects. No significant differences were found in any GSH redox measures between control subjects and individuals with other types of psychiatric disorders. There were, however, positive correlations between GSH and GPx, GSH and GR, as well as GPx and GR levels in control subjects without psychiatric disorders. These positive correlations suggest a dynamic state is kept in check during the redox coupling under normal conditions. By contrast, lack of such correlations in schizophrenia point to a disturbance of redox coupling mechanisms in the antioxidant defense system, possibly resulting from a decreased level of GSH as well as age-related decreases of GSSG and GR activities.

Highlights

  • Biological systems have evolved complex protective strategies against free radical toxicity [1]

  • There are no significant differences of age, postmortem interval (PMI), and storage time among three test groups with exception that brain weights was found significantly higher in schizophrenic than in control samples without psychiatric disorders

  • As expected, the frequency of smoking was higher in patients with either schizophrenia or bipolar and/or depression than in control subjects without psychiatric disorders

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Summary

Introduction

Biological systems have evolved complex protective strategies against free radical toxicity [1]. Under physiological conditions the potential for free radicalmediated damage is kept in check by the antioxidant defense system, comprising a series of enzymatic and non-enzymatic components (Fig. 1). The key antioxidant enzymes include superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px). Superoxide dismutase catalyzes the conversion of superoxide radicals (O−2 ) to hydrogen peroxide (H2O2), which in turn can form the highly reactive hydroxyl radicals. Catalase and glutathione peroxidase convert hydrogen peroxide to water. Glutathione (GSH) is utilized by GSH-Px to yield the oxidized form of glutathione (GSSG), which is converted back to GSH by glutathione reductase (GR). Nitric oxide (NO) which is the product of a five-electron oxidation

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