Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo
Do, K. Q. ; Trabesinger, A. H. ; Kirsten-Krüger, M. ; Lauer, C. J. ; Dydak, U. ; Hell, D. ; Holsboer, F. ; Boesiger, P. ; Cuénod, M.
Oxford, UK : Blackwell Science Ltd
Published 2000
Oxford, UK : Blackwell Science Ltd
Published 2000
ISSN: |
1460-9568
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Source: |
Blackwell Publishing Journal Backfiles 1879-2005
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Topics: |
Medicine
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Notes: |
Schizophrenia is a major psychiatric disease, which affects the centre of the personality, with severe problems of perception, cognition as well as affective and social behaviour. In cerebrospinal fluid of drug-free schizophrenic patients, a significant decrease in the level of total glutathione (GSH) by 27% (P 〈 0.05) was observed as compared to controls, in keeping with the reported reduced level of its metabolite γ-glutamylglutamine. With a new non-invasive proton magnetic resonance spectroscopy methodology, GSH level in medial prefrontal cortex of schizophrenic patients was found to be 52% (P = 0.0012) lower than in controls. GSH plays a fundamental role in protecting cells from damage by reactive oxygen species generated among others by the metabolism of dopamine. A deficit in GSH would lead to degenerative processes in the surrounding of dopaminergic terminals resulting in loss of connectivity. GSH also potentiates the N-methyl-d-aspartate (NMDA) receptor response to glutamate, an effect presumably reduced by a GSH deficit, leading to a situation similar to the application of phencyclidine (PCP). Thus, a GSH hypothesis might integrate many established biological aspects of schizophrenia.
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Type of Medium: |
Electronic Resource
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URL: |