Effects of acute N-acetylcysteine challenge on cortical glutathione and glutamate in schizophrenia: A pilot in vivo proton magnetic resonance spectroscopy study.

TitleEffects of acute N-acetylcysteine challenge on cortical glutathione and glutamate in schizophrenia: A pilot in vivo proton magnetic resonance spectroscopy study.
Publication TypeJournal Article
Year of Publication2019
AuthorsGirgis RR, Baker S, Mao X, Gil R, Javitt DC, Kantrowitz JT, Gu M, Spielman DM, Ojeil N, Xu X, Abi-Dargham A, Shungu DC, Kegeles LS
JournalPsychiatry Res
Volume275
Pagination78-85
Date Published2019 05
ISSN1872-7123
KeywordsAcetylcysteine, Adolescent, Adult, Female, Free Radical Scavengers, Glutamic Acid, Glutathione, Gyrus Cinguli, Humans, Male, Middle Aged, Prefrontal Cortex, Proton Magnetic Resonance Spectroscopy, Schizophrenia, Young Adult
Abstract

Findings from in vivo brain proton magnetic resonance spectroscopy (H MRS) and preclinical studies have suggested region- and medication status-dependent increases in glutamate (Glu) levels and deficiencies in glutathione (GSH) levels in schizophrenia. N-acetylcysteine (NAC), a GSH synthesis precursor, has demonstrated modest clinical benefit in schizophrenia. The objective of this study was to examine the effects of acute administration of NAC on GSH and Glu levels measured with H MRS in 19 patients with schizophrenia and 20 healthy control subjects. Levels of GSH were acquired in dorsal anterior cingulate cortex (dACC), and those of Glu in dACC and medial prefrontal cortex (mPFC), at baseline and 60 min following acute oral administration of 2400 mg of NAC. No differences in the levels of GSH or Glu were found at baseline or following NAC administration between patients with schizophrenia and control subjects in either of the targeted brain regions. Future studies measuring GSH levels in brain regions previously found to exhibit glutamatergic abnormalities or using genetic polymorphisms, while controlling for the age and medication status of the cohorts, are warranted to better identify groups of patients more likely to respond to NAC and its mode of action and mechanisms.

DOI10.1016/j.psychres.2019.03.018
Alternate JournalPsychiatry Res
PubMed ID30884334
PubMed Central IDPMC6515541
Grant ListR01 MH100005 / MH / NIMH NIH HHS / United States
S10 OD021782 / OD / NIH HHS / United States
R01 MH110683 / MH / NIMH NIH HHS / United States
R21 MH099508 / MH / NIMH NIH HHS / United States
R01 MH075895 / MH / NIMH NIH HHS / United States
P41 EB015891 / EB / NIBIB NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065