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Neurotherapeutics. 2019 Dec 20. doi: 10.1007/s13311-019-00817-1. [Epub ahead of print]

Alcohol Use Disorder Interventions Targeting Brain Sites for Both Conditioned Reward and Delayed Gratification.

Oberlin BG1,2,3,4, Shen YI5,6, Kareken DA5,6,7.

Author information

1
Department of Psychiatry, Indiana University School of Medicine, Indianapolis, USA. boberlin@iupui.edu.
2
Department of Neurology, Indiana University School of Medicine, Indianapolis,, USA. boberlin@iupui.edu.
3
Addiction Neuroscience Program, Department of Psychology, Indiana University Purdue University at Indianapolis, School of Science, Indianapolis, USA. boberlin@iupui.edu.
4
Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, USA. boberlin@iupui.edu.
5
Department of Psychiatry, Indiana University School of Medicine, Indianapolis, USA.
6
Department of Neurology, Indiana University School of Medicine, Indianapolis,, USA.
7
Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, USA.

Abstract

Alcohol use disorder is a destructive compulsion characterized by chronic relapse and poor recovery outcomes. Heightened reactivity to alcohol-associated stimuli and compromised executive function are hallmarks of alcohol use disorder. Interventions targeting these two interacting domains are thought to ameliorate these altered states, but the mutual brain sites of action are yet unknown. Although interventions on alcohol cue reactivity affect reward area responses, how treatments alter brain responses when subjects exert executive effort to delay gratification is not as well-characterized. Focusing on interventions that could be developed into effective clinical treatments, we review and identify brain sites of action for these two categories of potential therapies. Using activation likelihood estimation (ALE) meta-analysis, we find that interventions on alcohol cue reactivity localize to ventral prefrontal cortex, dorsal anterior cingulate, and temporal, striatal, and thalamic regions. Interventions for increasing delayed reward preference elicit changes mostly in midline default mode network regions, including posterior cingulate, precuneus, and ventromedial prefrontal cortex-in addition to temporal and parietal regions. Anatomical co-localization of effects appears in the ventromedial prefrontal cortex, whereas effects specific to delay-of-gratification appear in the posterior cingulate and precuneus. Thus, the current available literature suggests that interventions in the domains of cue reactivity and delay discounting alter brain activity along midline default mode regions, specifically in the ventromedial prefrontal cortex for both domains, and the posterior cingulate/precuneus for delay-of-gratification. We believe that these findings could facilitate targeting and development of new interventions, and ultimately treatments of this challenging disorder.

KEYWORDS:

Meta analysis; addiction; alcoholism; cues; ethanol; impulsivity; intertemporal choice

PMID:
31863407
DOI:
10.1007/s13311-019-00817-1

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