Alcohol Cue–Induced Ventral Striatum Activity Predicts Subsequent Alcohol Self‐Administration
Autor: | Lindsay R. Meredith, Elizabeth M. Burnette, Suzanna Donato, Alexandra Venegas, Lara A. Ray, ReJoyce Green, Aaron C. Lim, Erica N. Grodin |
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Rok vydání: | 2020 |
Předmět: |
Adult
Male Taste Genotype Receptors Opioid mu 030508 substance abuse Medicine (miscellaneous) Self Administration Alcohol Toxicology Placebo Gyrus Cinguli Aldehyde Dehydrogenase 1 Family Article Naltrexone Random Allocation Young Adult 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Thalamus Neuroimaging Humans Medicine Proportional Hazards Models Neural correlates of consciousness Ethanol business.industry Aldehyde Dehydrogenase Mitochondrial Functional Neuroimaging Ventral striatum Central Nervous System Depressants Magnetic Resonance Imaging Psychiatry and Mental health medicine.anatomical_structure chemistry Ventral Striatum Multilevel Analysis Female Cues 0305 other medical science Self-administration business Alcohol-Related Disorders 030217 neurology & neurosurgery Alcohol Deterrents Clinical psychology medicine.drug |
Zdroj: | Alcohol Clin Exp Res |
ISSN: | 1530-0277 0145-6008 |
DOI: | 10.1111/acer.14342 |
Popis: | Author(s): Lim, Aaron C; Green, ReJoyce; Grodin, Erica N; Venegas, Alexandra; Meredith, Lindsay R; Donato, Suzanna; Burnette, Elizabeth; Ray, Lara A | Abstract: BackgroundHuman 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.MethodsNon-treatment-seeking heavy drinkers of East Asian descent (nn=n41) completed a randomized, placebo-controlled, double-blind, crossover experiment on the effects of naltrexone on neuroimaging and human laboratory paradigms. Participants completed 5ndays 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.ResultsMultilevel Cox regressions indicated a significant effect of taste cue-elicited ventral striatum activation on latency to first drink, Wald χ2 n=n2.88, pn=n0.05, 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)n=n5.90, 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.ConclusionsNeuroimaging 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. |
Databáze: | OpenAIRE |
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