Granger causality reveals a dominant role of memory circuit in chronic opioid dependence

Addict Biol. 2017 Jul;22(4):1068-1080. doi: 10.1111/adb.12390. Epub 2016 Mar 14.

Abstract

Resting-state magnetic resonance imaging has uncovered abnormal functional connectivity in heroin-dependent individuals (HDIs). However, it remains unclear how brain regions implicated in addictions are related in baseline state without conditioned cues in heroin dependent individuals during opioid maintenance treatment (HDIs-OMT). Previous connectivity analysis assessed the strength of correlated activity between brain regions but lacked the ability to infer directional neural interactions. In the current study, we employed Granger causality analysis to investigate directional causal influences among the brain circuits in HDIs-OMT and non-opioid users. The results revealed a weaker effective connectivity between the caudate nucleus implicated in mediating the reward circuit and other brain regions and also a weaker connectivity between the anterior cingulate cortex and medial prefrontal cortex implicated in mediating inhibitory control. Conversely, HDIs-OMT exhibited stronger effective connectivity between the hippocampus and amygdala implicated in mediating learning-memory, and the anterior cingulate cortex involved in mediating inhibitory control while the putamen mediated learned habits, suggesting that the hippocampus and amygdala may propel the memory circuit to override the control circuit and drive the learned habit in HDIs-OMT. Alterations in learning-memory and inhibitory control may contribute jointly and form a basis for relapse risk even after a period of heroin abstinence. Sustained neural effect of opioid dependence on methadone maintenance including hyperactivation in the memory circuit and impairment in the control circuit support the role of the memory circuitry in relapse and may help redefine targets for treatment.

Keywords: Granger causality; inhibitory control; learning-memory; opioid dependence; resting-state fMRI.

MeSH terms

  • Adult
  • Amygdala / diagnostic imaging
  • Amygdala / drug effects
  • Amygdala / physiopathology
  • Brain / diagnostic imaging
  • Brain / drug effects*
  • Brain / physiopathology*
  • Brain Mapping / methods*
  • Gyrus Cinguli / diagnostic imaging
  • Gyrus Cinguli / drug effects
  • Gyrus Cinguli / physiopathology
  • Hippocampus / diagnostic imaging
  • Hippocampus / drug effects
  • Hippocampus / physiopathology
  • Humans
  • Magnetic Resonance Imaging / methods*
  • Male
  • Memory / physiology
  • Memory Disorders / chemically induced*
  • Memory Disorders / diagnostic imaging
  • Memory Disorders / physiopathology*
  • Middle Aged
  • Opioid-Related Disorders / complications*
  • Opioid-Related Disorders / physiopathology
  • Prefrontal Cortex / diagnostic imaging
  • Prefrontal Cortex / physiopathology
  • Putamen / diagnostic imaging
  • Putamen / drug effects
  • Putamen / physiopathology
  • Rest