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Mesocorticolimbic system reactivity to alcohol use-related visual cues as a function of alcohol sensitivity phenotype: A pilot fMRI study
被引:2
|作者:
Cofresi, Roberto U.
[1
]
Upton, Spencer
[1
]
Brown, Alexander A.
[1
]
Piasecki, Thomas M.
[2
]
Bartholow, Bruce D.
[3
]
Froeliger, Brett
[1
,4
]
机构:
[1] Univ Missouri, Dept Psychol Sci, Columbia, MO 65211 USA
[2] Univ Wisconsin Madison, Ctr Tobacco Res & Intervent, Dept Med, Madison, WI USA
[3] Univ Iowa, Dept Psychol & Brain Sci, Iowa City, IA USA
[4] Univ Missouri Columbia, Dept Psychiat, Columbia, MO USA
来源:
关键词:
Alcohol;
Incentive;
Fronto-striatal;
Sensitization;
Level of response;
INCENTIVE-SENSITIZATION THEORY;
IDENTIFICATION TEST AUDIT;
INDIVIDUAL VARIATION;
BASAL GANGLIA;
DRUG-ADDICTION;
MOTIVATIONAL PROPERTIES;
NEUROBIOLOGICAL BASIS;
POTENTIAL REACTIVITY;
SUBJECTIVE RESPONSE;
NEURAL BASIS;
D O I:
10.1016/j.addicn.2024.100156
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Low sensitivity (LS) to alcohol is a risk factor for alcohol use disorder (AUD). Compared to peers with high sensitivity (HS), LS individuals drink more, report more problems, and exhibit potentiated alcohol cue reactivity (ACR). Heightened ACR suggests LS confers AUD risk via incentive sensitization, which is thought to take place in the mesocorticolimbic system. This study examined neural ACR in LS and HS individuals. Young adults (N = 32, Mage=20.3) were recruited based on the Alcohol Sensitivity Questionnaire (HS: n = 16; LS: n = 16; 9 females/ group). Participants completed an event-related fMRI ACR task. Group LS had higher ACR in left ventrolateral prefrontal cortex than group HS. In group LS, ACR in left caudomedial orbitofrontal cortex or left putamen was low at low alcohol use levels and high at heavier or more problematic alcohol use levels, whereas the opposite was true in group HS. Alcohol use level also was associated with the level of ACR in left substantia nigra among males in group LS. Taken together, results suggest elevated mesocorticolimbic ACR among LS individuals, especially those using alcohol at hazardous levels. Future studies with larger samples are warranted to determine the neurobiological loci underlying LS-based amplified ACR and AUD risk.
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