Glutathione precursor, N-acetyl-cysteine, improves mismatch negativity in schizophrenia patients - PubMed (original) (raw)

Randomized Controlled Trial

. 2008 Aug;33(9):2187-99.

doi: 10.1038/sj.npp.1301624. Epub 2007 Nov 14.

Micah M Murray, Patricia Deppen, Maria G Knyazeva, Michael Berk, Olivier Boulat, Pierre Bovet, Ashley I Bush, Philippe Conus, David Copolov, Eleonora Fornari, Reto Meuli, Alessandra Solida, Pascal Vianin, Michel Cuénod, Thierry Buclin, Kim Q Do

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Randomized Controlled Trial

Glutathione precursor, N-acetyl-cysteine, improves mismatch negativity in schizophrenia patients

Suzie Lavoie et al. Neuropsychopharmacology. 2008 Aug.

Abstract

In schizophrenia patients, glutathione dysregulation at the gene, protein and functional levels, leads to N-methyl-D-aspartate (NMDA) receptor hypofunction. These patients also exhibit deficits in auditory sensory processing that manifests as impaired mismatch negativity (MMN), which is an auditory evoked potential (AEP) component related to NMDA receptor function. N-acetyl-cysteine (NAC), a glutathione precursor, was administered to patients to determine whether increased levels of brain glutathione would improve MMN and by extension NMDA function. A randomized, double-blind, cross-over protocol was conducted, entailing the administration of NAC (2 g/day) for 60 days and then placebo for another 60 days (or vice versa). 128-channel AEPs were recorded during a frequency oddball discrimination task at protocol onset, at the point of cross-over, and at the end of the study. At the onset of the protocol, the MMN of patients was significantly impaired compared to sex- and age- matched healthy controls (p=0.003), without any evidence of concomitant P300 component deficits. Treatment with NAC significantly improved MMN generation compared with placebo (p=0.025) without any measurable effects on the P300 component. MMN improvement was observed in the absence of robust changes in assessments of clinical severity, though the latter was observed in a larger and more prolonged clinical study. This pattern suggests that MMN enhancement may precede changes to indices of clinical severity, highlighting the possible utility AEPs as a biomarker of treatment efficacy. The improvement of this functional marker may indicate an important pathway towards new therapeutic strategies that target glutathione dysregulation in schizophrenia.

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