Enhanced conditioned "liking" of novel visual cues paired with alcohol or non-alcohol beverage container images among individuals at higher risk for alcohol use disorder.
Enhanced conditioned "liking" of novel visual cues paired with alcohol or non-alcohol beverage container images among individuals at higher risk for alcohol use disorder.
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DOI:
10.1007/s00213-022-06231-4
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发表时间:
2022-11
影响因子:
3.4
通讯作者:
Schachtman, Todd R.
中科院分区:
文献类型:
--
作者:
Cofresi, Roberto U.;Piasecki, Thomas M.;Bartholow, Bruce D.;Schachtman, Todd R.
This study used an evaluative conditioning (EC) procedure to assess the affective properties of a CS for ingested drug reward in humans. Specifically, the study tested whether the evaluative response (“liking”/”disliking”) to an arbitrary visual stimulus (“CS2,” e.g., a purple hexagon) could be changed through pairings with an alcohol or non-alcohol beverage cue (“CS1,” e.g., a full wine glass, a juice box), which is ostensibly a conditioned visual predictive stimulus for alcohol or non-alcohol liquid reward, respectively. Participants (N = 369, 18–23 years, 66% female, 79% white, 21% reporting no alcohol use ever or in the past year) received 24 CS1 pairings with each CS2. CS2 and CS1 evaluations were assessed pre- and post-conditioning. Alcohol and non-alcohol CS2 “liking” correlated with alcohol use. “Liking” of the alcohol but not non-alcohol CS1 also correlated with alcohol use. Alcohol CS1 “liking” also correlated with alcohol and non-alcohol CS2 ‘liking,” whereas non-alcohol CS1 ‘liking” correlated with non-alcohol but not alcohol CS2 “liking.” Taken together, findings support the idea that drug-related visual stimuli acquire appetitive (hedonic and/or incentive) properties as a function of individual differences in drug use, which entail individual differences in exposure to the conditioning effects of addictive substances like alcohol. Findings also suggest a link between drug use and the propensity to attribute affective/motivational significance to reward-predictive cues in general. The online version contains supplementary material available at 10.1007/s00213-022-06231-4.
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