Abstract
Continued seeking and drinking of alcohol despite adverse legal, health, economic, and societal consequences
is a central hallmark of human alcohol use disorders. This compulsive drive for alcohol, defined
by resistance to adverse and deleterious consequences, represents a major challenge when attempting to
treat alcoholism clinically. Thus, there has long been interest in developing pre-clinical rodent models for
the compulsive drug use that characterizes drug addiction. Here, we review recent studies that have
attempted to model compulsive aspects of alcohol and cocaine intake in rodents, and consider technical
and conceptual issues that need to be addressed when trying to recapitulate compulsive aspects of
human addiction. Aversion-resistant alcohol intake has been examined by pairing intake or seeking with
the bitter tastant quinine or with footshock, and exciting recent work has used these models to identify
neuroadaptations in the amygdala, cortex, and striatal regions that promote compulsive intake. Thus,
rodent models do seem to reflect important aspects of compulsive drives that sustain human addiction,
and will likely provide critical insights into the molecular and circuit underpinnings of aversion-resistant
intake as well as novel therapeutic interventions for compulsive aspects of addiction.
is a central hallmark of human alcohol use disorders. This compulsive drive for alcohol, defined
by resistance to adverse and deleterious consequences, represents a major challenge when attempting to
treat alcoholism clinically. Thus, there has long been interest in developing pre-clinical rodent models for
the compulsive drug use that characterizes drug addiction. Here, we review recent studies that have
attempted to model compulsive aspects of alcohol and cocaine intake in rodents, and consider technical
and conceptual issues that need to be addressed when trying to recapitulate compulsive aspects of
human addiction. Aversion-resistant alcohol intake has been examined by pairing intake or seeking with
the bitter tastant quinine or with footshock, and exciting recent work has used these models to identify
neuroadaptations in the amygdala, cortex, and striatal regions that promote compulsive intake. Thus,
rodent models do seem to reflect important aspects of compulsive drives that sustain human addiction,
and will likely provide critical insights into the molecular and circuit underpinnings of aversion-resistant
intake as well as novel therapeutic interventions for compulsive aspects of addiction.
Original language | English |
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Pages (from-to) | 253-264 |
Number of pages | 12 |
Journal | Alcohol |
Volume | 48 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2014 |
Keywords
- Compulsion
- Addiction
- Aversion
- Punishment
- Alcohol
- Striatum
- Accumbens
- Central amygdala
- Cortex
- Adaptation
- Ion channel
- Glutamate receptor
- Intracellular signaling
- Circuit