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Altered anterior cingulate cortex to hippocampus effective connectivity in response to drug cues in men with cocaine use disorder. | LitMetric

Altered anterior cingulate cortex to hippocampus effective connectivity in response to drug cues in men with cocaine use disorder.

Psychiatry Res Neuroimaging

Institute for Drug and Alcohol Studies, Richmond, VA, USA; Department of Psychiatry, Virginia Commonwealth University (VCU), Richmond, VA, USA; Department of Pharmacology and Toxicology, Richmond, VA, USA; Department of Neurology, VCU, Richmond, VA, USA.

Published: January 2018

Drug-related attentional bias may have significant implications for the treatment of cocaine use disorder (CocUD). However, the neurobiology of attentional bias is not completely understood. This study employed dynamic causal modeling (DCM) to conduct an analysis of effective (directional) connectivity involved in drug-related attentional bias in treatment-seeking CocUD subjects. The DCM analysis was conducted based on functional magnetic resonance imaging (fMRI) data acquired from fifteen CocUD subjects while performing a cocaine-word Stroop task, during which blocks of Cocaine Words (CW) and Neutral Words (NW) alternated. There was no significant attentional bias at group level. Although no significant brain activation was found, the DCM analysis found that, relative to the NW, the CW caused a significant increase in the strength of the right (R) anterior cingulate cortex (ACC) to R hippocampus effective connectivity. Greater increase of this connectivity was associated with greater CW reaction time (relative to NW reaction time). The increased strength of R ACC to R hippocampus connectivity may reflect ACC activation of hippocampal memories related to drug use, which was triggered by the drug cues. This circuit could be a potential target for therapeutics in CocUD patients. No significant change was found in the other modeled connectivities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741507PMC
http://dx.doi.org/10.1016/j.pscychresns.2017.10.012DOI Listing

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