Alcohol Cue-Induced Ventral Striatum Activity Predicts Subsequent Alcohol Self-Administration

Alcohol Clin Exp Res. 2020 Jun;44(6):1224-1233. doi: 10.1111/acer.14342. Epub 2020 May 14.

Abstract

Background: Human laboratory paradigms are a pillar in medication development for alcohol use disorders (AUD). Neuroimaging paradigms, in which individuals are exposed to cues that elicit neural correlates of alcohol craving (e.g., mesocorticolimbic activation), are increasingly utilized to test the effects of AUD medications. Elucidation of the translational effects of these neuroimaging paradigms on human laboratory paradigms, such as self-administration, is warranted. The current study is a secondary analysis examining whether alcohol cue-induced activation in the ventral striatum is predictive of subsequent alcohol self-administration in the laboratory.

Methods: Non-treatment-seeking heavy drinkers of East Asian descent (n = 41) completed a randomized, placebo-controlled, double-blind, crossover experiment on the effects of naltrexone on neuroimaging and human laboratory paradigms. Participants completed 5 days of study medication (or placebo); on day 4, they completed a neuroimaging alcohol taste cue-reactivity task. On the following day (day 5), participants completed a 60-minute alcohol self-administration paradigm.

Results: Multilevel Cox regressions indicated a significant effect of taste cue-elicited ventral striatum activation on latency to first drink, Wald χ2 = 2.88, p = 0.05, such that those with higher ventral striatum activation exhibited shorter latencies to consume their first drink. Similarly, ventral striatum activation was positively associated with total number of drinks consumed, F(1, 38) = 5.90, p = 0.02. These effects were significant after controlling for alcohol use severity, OPRM1 genotype, and medication. Other potential regions of interest (anterior cingulate, thalamus) were not predictive of self-administration outcomes.

Conclusions: Neuroimaging alcohol taste cue paradigms may be predictive of laboratory paradigms such as self-administration. Elucidation of the relationships among different paradigms will inform how these paradigms may be used synergistically in experimental medicine and medication development.

Keywords: Alcohol Self-administration; Cue-Induced Craving; Human Laboratory; Neuroimaging; Ventral Striatum.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Alcohol Deterrents / pharmacology
  • Alcohol-Related Disorders / diagnostic imaging*
  • Alcohol-Related Disorders / physiopathology
  • Aldehyde Dehydrogenase 1 Family / genetics
  • Aldehyde Dehydrogenase, Mitochondrial / genetics
  • Central Nervous System Depressants / administration & dosage*
  • Cues*
  • Ethanol / administration & dosage*
  • Female
  • Functional Neuroimaging
  • Genotype
  • Gyrus Cinguli / diagnostic imaging
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Multilevel Analysis
  • Naltrexone / pharmacology
  • Proportional Hazards Models
  • Random Allocation
  • Receptors, Opioid, mu / genetics
  • Self Administration
  • Thalamus / diagnostic imaging
  • Ventral Striatum / diagnostic imaging*
  • Ventral Striatum / drug effects
  • Ventral Striatum / physiopathology
  • Young Adult

Substances

  • Alcohol Deterrents
  • Central Nervous System Depressants
  • OPRM1 protein, human
  • Receptors, Opioid, mu
  • Ethanol
  • Naltrexone
  • Aldehyde Dehydrogenase 1 Family
  • Aldehyde Dehydrogenase, Mitochondrial