Literature DB >> 23911441

Tales from the dark side: do neuromodulators of drug withdrawal require changes in endocannabinoid tone?

Erik B Oleson1, Roger Cachope2, Aurelie Fitoussi2, Joseph F Cheer3.   

Abstract

Environmental and interoceptive cues are theorized to serve as 'signals' that motivate drug seeking and effects that may be augmented in the withdrawn state. Phasic dopamine release events are observed in the nucleus accumbens in response to such motivational salient stimuli and are thought to be necessary for drug-associated cues to trigger craving. We recently demonstrated how dopamine neurons encode stimuli conditioned to a negative event, as might occur during conditioned withdrawal, and stimuli predicting the avoidance of negative events, as might occur as an addict seeks out drugs to prevent withdrawal. In this review we first discuss how the subsecond dopamine release events might process conditioned withdrawal and drug seeking driven by negative reinforcement processes within the context of our dopamine data obtained during conditioned avoidance procedures. We next describe how the endocannabinoid system modulates phasic dopamine release events and how it might be harnessed to treat negative affective states in addiction. Specifically, we have demonstrated that endocannabinoids in the ventral tegmentum sculpt cue-induced accumbal surges in dopamine release and, therefore, may also be mobilized during drug withdrawal.
© 2013.

Entities:  

Keywords:  Addiction; Avoidance; Dependence; Dopamine; Endocannabinoid

Mesh:

Substances:

Year:  2013        PMID: 23911441      PMCID: PMC3874071          DOI: 10.1016/j.pnpbp.2013.07.019

Source DB:  PubMed          Journal:  Prog Neuropsychopharmacol Biol Psychiatry        ISSN: 0278-5846            Impact factor:   5.067


  89 in total

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Authors:  A R Childress; A T McLellan; R Ehrman; C P O'Brien
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5.  Cocaine cues and dopamine in dorsal striatum: mechanism of craving in cocaine addiction.

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Review 9.  Incubation of cocaine craving after withdrawal: a review of preclinical data.

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