In vivo effects of ketamine on glutamate-glutamine and gamma-aminobutyric acid in obsessive-compulsive disorder: Proof of concept.

TitleIn vivo effects of ketamine on glutamate-glutamine and gamma-aminobutyric acid in obsessive-compulsive disorder: Proof of concept.
Publication TypeJournal Article
Year of Publication2015
AuthorsRodriguez CI, Kegeles LS, Levinson A, R Ogden T, Mao X, Milak MS, Vermes D, Xie S, Hunter L, Flood P, Moore H, Shungu DC, Simpson HB
JournalPsychiatry Res
Volume233
Issue2
Pagination141-7
Date Published2015 Aug 30
ISSN1872-7123
KeywordsAdult, Cross-Over Studies, Excitatory Amino Acid Antagonists, Female, gamma-Aminobutyric Acid, Glutamic Acid, Glutamine, Humans, Ketamine, Male, Obsessive-Compulsive Disorder, Prefrontal Cortex, Proton Magnetic Resonance Spectroscopy, Treatment Outcome
Abstract

We previously reported the rapid and robust clinical effects of ketamine versus saline infusions in a proof-of-concept crossover trial in unmedicated adults with obsessive-compulsive disorder (OCD). This study examined the concurrent neurochemical effects of ketamine versus saline infusions using proton magnetic resonance spectroscopy ((1)H MRS) during the clinical proof-of-concept crossover trial. Levels of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) and the excitatory neurochemicals glutamate+glutamine (Glx) were acquired in the medial prefrontal cortex (MPFC), a region implicated in OCD pathology. Seventeen unmedicated OCD adults received two intravenous infusions at least 1 week apart, one of saline and one of ketamine, while lying supine in a 3.0 T GE MR scanner. The order of each infusion pair was randomized. Levels of GABA and Glx were measured in the MPFC before, during, and after each infusion and normalized to water (W). A mixed effects model found that MPFC GABA/W significantly increased over time in the ketamine compared with the saline infusion. In contrast, there were no significant differences in Glx/W between the ketamine and saline infusions. Together with earlier evidence of low cortical GABA in OCD, our findings suggest that models of OCD pathology should consider the role of GABAergic abnormalities in OCD symptomatology.

DOI10.1016/j.pscychresns.2015.06.001
Alternate JournalPsychiatry Res
PubMed ID26104826
PubMed Central IDPMC4715460
Grant ListK24 MH091555 / MH / NIMH NIH HHS / United States
K23MH092434 / MH / NIMH NIH HHS / United States
K24MH09155 / MH / NIMH NIH HHS / United States
UL1TR000040 / TR / NCATS NIH HHS / United States
UL1 TR000040 / TR / NCATS NIH HHS / United States
K23 MH092434 / MH / NIMH NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

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