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Choosing Money over Drugs: The Neural Underpinnings of Difficult Choice in Chronic Cocaine Users
Author(s) -
Michael J. Wesley,
Terry Lohrenz,
Mikhail N. Koffarnus,
Samuel M. McClure,
Richard De La Garza,
Ramiro Salas,
Daisy G.Y. Thompson-Lake,
Thomas F. Newton,
Warren K. Bickel,
P. Read Montague
Publication year - 2014
Publication title -
journal of addiction
Language(s) - English
Resource type - Journals
eISSN - 2090-7834
pISSN - 2090-7850
DOI - 10.1155/2014/189853
Subject(s) - addiction , dorsolateral prefrontal cortex , striatum , neuroimaging , ventral striatum , dorsum , neuroscience , psychology , impulsivity , prefrontal cortex , medicine , developmental psychology , cognition , dopamine , anatomy
Addiction is considered a disorder that drives individuals to choose drugs at the expense of healthier alternatives. However, chronic cocaine users (CCUs) who meet addiction criteria retain the ability to choose money in the presence of the opportunity to choose cocaine. The neural mechanisms that differentiate CCUs from non-cocaine using controls (Controls) while executing these preferred choices remain unknown. Thus, therapeutic strategies aimed at shifting preferences towards healthier alternatives remain somewhat uninformed. This study used BOLD neuroimaging to examine brain activity as fifty CCUs and Controls performed single- and cross-commodity intertemporal choice tasks for money and/or cocaine. Behavioral analyses revealed preferences for each commodity type. Imaging analyses revealed the brain activity that differentiated CCUs from Controls while choosing money over cocaine. We observed that CCUs devalued future commodities more than Controls. Choices for money as opposed to cocaine correlated with greater activity in dorsal striatum of CCUs, compared to Controls. In addition, choices for future money as opposed to immediate cocaine engaged the left dorsolateral prefrontal cortex (DLPFC) of CCUs more than Controls. These data suggest that the ability of CCUs to execute choices away from cocaine relies on activity in the dorsal striatum and left DLPFC.

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