4.5 Article

Targeting dopamine D2 and Cannabinoid-1 (CB1) receptors in rat nucleus accumbens

Journal

JOURNAL OF COMPARATIVE NEUROLOGY
Volume 495, Issue 3, Pages 299-313

Publisher

WILEY
DOI: 10.1002/cne.20881

Keywords

marijuana; motor inhibition; reward; drug addiction; basal ganglia

Funding

  1. NIDA NIH HHS [P60 DA005130-229006, DA00286, R01 DA004600, R01 DA004600-18, K02 DA000286, P60 DA005130, DA11322, DA 04600, R01 DA011322] Funding Source: Medline
  2. PHS HHS [005130] Funding Source: Medline

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The nucleus accumbens (Acb) shell and core are essential components of neural circuitry mediating the reward and motor effects produced by activation of dopamine D2 or cannabinoid-1 (CB1) receptors. D2 receptors can form heterodimeric complexes with cannabinoid-1 (CB1) receptors and are also involved in control of the availability of both dopamine and endocannabinoids. Thus, the subcellular locations of D2 and CB1 receptors with respect to each other are implicit to their physiological actions in the Acb. We used electron microscopic immunocytochemistry to determine these locations in the Acb shell and core of rat brain. In each region, many neuronal profiles showed endomembrane and plasmalemmal distributions of one or both receptors. Approximately one-third of the labeled profiles were somata and dendrites, some of which showed overlapping subeellular distributions of D2 and CB1 immunoreactivities. The remaining labeled profiles were small axons and axon terminals containing CB1 and/or D2 receptors. Of the labeled terminals forming recognizable synapses, similar to 20% of those containing CB1 receptors contacted D2-labeled dendrites, while conversely, almost 15% of those containing D2 receptors contacted CB1-labeled dendrites. These results provide the first ultrastructural evidence that D2 and CB1 receptors in the Acb shell and core have subeellular distributions supporting both intracellular associations and local involvement of D2 receptors in making available endocannabinoids that are active on CB1 receptors in synaptic neurons. These distributions have direct relevance to the rewarding and euphoric as well as motor effects produced by marijuana and by addictive drugs enhancing dopamine levels in the Acb.

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