The ventral tegmental area dopamine to basolateral amygdala projection supports acquisition of cocaine self-administration.

Neuropharmacology

Department of Psychiatry, University of Pittsburgh, 450 Technology Drive, Pittsburgh, PA, 15219, USA; Center for Neuroscience, University of Pittsburgh, 4200 Fifth Ave, Pittsburgh, PA, 15213, USA. Electronic address:

Published: December 2024

AI Article Synopsis

  • Dopamine signaling in the amygdala is crucial for associative learning, particularly in linking environmental cues to the effects of drugs like cocaine.
  • Researchers used chemogenetics to alter dopamine inputs from the ventral tegmental area (VTA) to the basolateral amygdala (BLA) during cocaine-related behaviors, revealing that inhibiting dopamine reduced the motivation to seek cocaine when exposed to previously associated cues.
  • The findings suggest that targeting dopamine pathways in the amygdala could lead to new treatments for substance use disorders by potentially modifying the associations formed between cues and drug use.

Article Abstract

Dopamine signaling in the amygdala is known to play a role in associative learning and memory, including the process of learning to associate environmental cues with the reinforcing properties of drugs like cocaine. Evidence suggests that the ventral tegmental area (VTA) dopamine (DA) projection specifically to the basolateral amygdala (BLA) participates in establishing cocaine-cue associations that can promote later craving- and relapse-like responses to the cue alone. In order to further investigate the specific role of VTA-BLA projections in cocaine-reinforced learning, we used chemogenetics to manipulate VTA DA inputs to the BLA during cocaine self-administration, cue- and cocaine-primed reinstatement, and conditioned place preference. We found inhibiting DA input to the BLA during cocaine self-administration inhibited acquisition and weakened the ability of the previously cocaine-paired cue to elicit cocaine-seeking, while acutely inhibiting the pathway on the day of cue-induced reinstatement testing had no effect. Conversely, exciting the projection during self-administration boosted the salience of the cocaine-paired cue as indicated by enhanced responding during cue-induced reinstatement. Importantly, interfering with DA input to the BLA had no impact on the ability of cocaine to elicit a place preference or induce reinstatement in response to a priming cocaine injection. Overall, we show that manipulation of projections underlying DA signaling in the BLA may be useful for developing therapeutic interventions for substance use disorders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11585075PMC
http://dx.doi.org/10.1016/j.neuropharm.2024.110160DOI Listing

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