Blunted neural reward response to alcohol and greater alcohol motivation in binge drinkers in a randomized clinical experiment

被引:3
|
作者
Blaine, Sara [1 ,2 ]
Fogelman, Nia [2 ]
Lacadie, Cheryl [3 ]
Constable, Todd [3 ]
Sinha, Rajita [2 ,4 ]
机构
[1] Auburn Univ, Dept Psychol Sci, Auburn, AL USA
[2] Yale Sch Med, Dept Psychiat, New Haven, CT USA
[3] Yale Sch Med, Dept Radiol & Biomed Imaging, New Haven, CT USA
[4] Yale Univ, Sch Med, Dept Psychiat, 2 Church St South,Suite 209, New Haven, CT 06519 USA
来源
基金
美国国家卫生研究院;
关键词
binge drinking; fMRI; motivation; orbitofrontal cortex; reward; PITUITARY-ADRENAL AXIS; CEREBRAL-BLOOD-FLOW; INTRAVENOUS ALCOHOL; PERFUSION; BRAIN; DRUG; DOPAMINE; HEAVY; PREDICTIONS; SENSITIVITY;
D O I
10.1111/acer.15082
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Alcohol stimulates cerebral blood flow (CBF) in brain reward regions. However, neural processes that support sustained alcohol motivation after the first drink are not well understood.Methods: Using a novel placebo-controlled, randomized, crossover experiment, 27 individuals who binge drink (BD; 15 M, 12 F) and 25 social drinkers (SD; 15 M, 10 F) underwent a behavioral test of self-motivated alcohol consumption using an Alcohol Taste Test (ATT) involving alcoholic and nonalcoholic beer on separate days. The test was followed immediately by perfusion functional magnetic resonance imaging (fMRI). On both days, participants then engaged in a post-scan ATT with placebo beer to assess sustained alcohol self-motivation without active alcohol effects. Linear mixed effects models were used to examine the effects of drinking group on the placebo-controlled effect of initial alcohol motivation on brain perfusion (whole brain corrected p < 0.001, cluster corrected p < 0.025) and on the relationship between placebo-controlled brain perfusion and sustained alcohol motivation.Results: Initial alcohol self-motivation in the alcohol relative to placebo session led to markedly decreased activation in the medial orbitofrontal cortex (OFC) and the ventral striatum in BD relative to SD, indicative of neural reward tolerance. The BD group also showed an enhanced neural response in behavioral intention regions of the supplementary motor area (SMA) and inferior frontal gyrus (IFG) regions. Moreover, there was greater sustained alcohol motivation in BD than SD in the post-scan ATT in the alcohol relative to placebo session. Correspondingly, only in BD and only in the alcohol session, lower alcohol-induced OFC response correlated with concurrent sensitized SMA response, and each predicted the subsequent sustained higher alcohol motivation in the post-scan ATT.Conclusions: Alcohol-related OFC tolerance may play an important role in sustained alcohol motivation. Furthermore, both specific alcohol-related neural reward tolerance and premotor sensitization responses may contribute to escalating alcohol motivation to drive excessive alcohol intake, even in individuals without alcohol use disorder.
引用
收藏
页码:1067 / 1078
页数:12
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