A combined spectroscopic and functional MRI investigation of the dorsal anterior cingulate region in opiate addiction

Mol Psychiatry. 2007 Jul;12(7):611, 691-702. doi: 10.1038/sj.mp.4001955. Epub 2007 Jan 23.

Abstract

Converging neuropsychological and functional neuroimaging evidence indicates that the dorsal anterior cingulate cortex (dACC) is dysfunctional in drug-addicted populations. Few studies, however, have investigated the biochemical and physiological properties of the dACC in such populations. We used proton magnetic resonance spectroscopy ((1)H-MRS) together with functional magnetic resonance imaging (fMRI) to probe dACC biochemistry and physiological activity during performance of a behavioural control task in 24 opiate-dependent individuals (maintained on a stable dose of methadone or buprenorphine at the time of study) and 24 age, gender, intelligence and performance-matched healthy subjects. While both groups activated the dACC to comparable levels, the opiate-using group displayed relatively increased task-related activation of frontal, parietal and cerebellar regions, as well as reduced concentrations of dACC N-acetylaspartate and glutamate/glutamine. In addition, the opiate-using group failed to show the expected correlations between dACC activation and behavioural measures of cognitive control. These findings suggest that the dACC is biochemically and physiologically abnormal in long-term opiate-dependent individuals. Furthermore, opiate addicts required increased, perhaps compensatory, involvement of the fronto-parietal and cerebellar behavioural regulation network to achieve normal levels of task performance/behavioural control. These neurobiological findings may partly underpin key addiction-related phenomena, such as poor inhibitory control of drug-related behaviour in the face of adverse consequences, and may be of relevance to the design of future treatment studies.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adaptation, Physiological
  • Adult
  • Analysis of Variance
  • Arousal / physiology*
  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / metabolism
  • Brain Mapping*
  • Case-Control Studies
  • Cerebellum / physiology
  • Cerebellum / physiopathology
  • Female
  • Frontal Lobe / physiology
  • Frontal Lobe / physiopathology
  • Glutamic Acid / metabolism
  • Glutamine / metabolism
  • Gyrus Cinguli / metabolism
  • Gyrus Cinguli / physiopathology*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Matched-Pair Analysis
  • Opioid-Related Disorders / metabolism
  • Opioid-Related Disorders / physiopathology*
  • Parietal Lobe / physiology
  • Parietal Lobe / physiopathology
  • Psychomotor Performance / physiology
  • Time Factors

Substances

  • Glutamine
  • Aspartic Acid
  • Glutamic Acid
  • N-acetylaspartate