Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo

Détails

ID Serval
serval:BIB_E163FEC5E7C2
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo
Périodique
European Journal of Neuroscience
Auteur⸱e⸱s
Do Kim Quang, Trabesinger Andreas Heinz, Kirsten-Krüger Monika, Lauer C.J., Dydak Ulrike, Hell Daniel, Holsboer F., Boesiger Peter, Cuénod Michel
ISSN
0953-816X
Statut éditorial
Publié
Date de publication
2000
Peer-reviewed
Oui
Volume
12
Numéro
10
Pages
3721-3728
Langue
anglais
Notes
DA - 20001103 IS - 0953-816X LA - eng PT - Journal Article RN - 0 (Reactive Oxygen Species) RN - 51-61-6 (Dopamine) RN - 70-18-8 (Glutathione) SB - IM Institution : Brain Research Institute, University of Zurich and Centre for Research in Psychiatric Neuroscience, University of Lausanne, Route de Cery, CH-1008 Prilly-Lausanne, Switzerland. Kim.Do@inst.hospvd.ch Mention de responsabiblité : Do,K.Q.;Trabesinger,A.H.;Kirsten-Kruger,M.;Lauer,C.J.;Dydak,U.;Hell,D.;Holsboer,F.;Boesiger,P.;Cuenod,M. SAPHIRID:48100
Résumé
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 gamma-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
Pubmed
Web of science
Création de la notice
10/03/2008 11:49
Dernière modification de la notice
20/08/2019 17:05
Données d'usage