Ethyl-eicosapentaenoic acid in first-episode psychosis. A 1H-MRS study

Neuropsychopharmacology. 2008 Sep;33(10):2467-73. doi: 10.1038/sj.npp.1301628. Epub 2008 Jan 16.

Abstract

Ethyl-eicosapentaenoic acid (E-EPA) is an omega-3 fatty acid that has been used in a range of neuropsychiatric conditions with some benefits. However, its mechanism of action is unknown. Here, we investigate its effects on in vivo brain metabolism in first-episode psychosis (FEP). Proton magnetic resonance spectroscopy at 3 T was performed in the temporal lobes of 24 FEP patients before and after 12 weeks of treatment in the context of a larger double-blind, placebo-controlled E-EPA augmentation study. Treatment group effects for glutathione (F1,12=6.1, p=0.03), and a hemisphere-by-group interaction for glutamine/glutamate (F1,20=4.4, p=0.049) were found. Glutathione increased bilaterally and glutamate/glutamine increased in the left hemisphere following E-EPA administration. Improvement in negative symptoms correlated with metabolic brain changes, particularly glutathione (r=-0.57). These results suggest that E-EPA augmentation alters glutathione availability and modulates the glutamine/glutamate cycle in early psychosis, with some of the metabolic brain changes being correlated with negative symptom improvement. Larger confirmatory studies of these postulated metabolic brain effects of E-EPA are warranted.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Brain / drug effects*
  • Brain / metabolism*
  • Brain / physiopathology
  • Brain Chemistry / drug effects*
  • Brain Chemistry / physiology
  • Brain Mapping
  • Dietary Supplements
  • Double-Blind Method
  • Eicosapentaenoic Acid / analogs & derivatives*
  • Eicosapentaenoic Acid / pharmacology
  • Eicosapentaenoic Acid / therapeutic use
  • Female
  • Glutamic Acid / metabolism
  • Glutamine / metabolism
  • Glutathione / metabolism
  • Humans
  • Magnetic Resonance Spectroscopy
  • Male
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Placebos
  • Psychotic Disorders / diagnosis
  • Psychotic Disorders / drug therapy*
  • Psychotic Disorders / metabolism*
  • Temporal Lobe / metabolism
  • Temporal Lobe / physiopathology
  • Time Factors
  • Treatment Outcome
  • Up-Regulation / drug effects
  • Up-Regulation / physiology

Substances

  • Placebos
  • Glutamine
  • Glutamic Acid
  • eicosapentaenoic acid ethyl ester
  • Eicosapentaenoic Acid
  • Glutathione