| Literature DB >> 32320647 |
Robert G Lewis1, Marcello Serra1, Daniela Radl1, Michela Gori1, Catherine Tran1, Sharon E Michalak2, Christopher D Vanderwal2, Emiliana Borrelli3.
Abstract
Cocaine drastically elevates dopamine (DA) levels in the striatum, a brain region that is critical to the psychomotor and rewarding properties of the drug. DA signaling regulates intrastriatal circuits connecting medium spiny neurons (MSNs) with afferent fibers and interneurons. While the cocaine-mediated increase in DA signaling on MSNs is well documented, that on cholinergic interneurons (ChIs) has been more difficult to assess. Using combined pharmacological, chemogenetic, and cell-specific ablation approaches, we reveal that the D2R-dependent inhibition of acetylcholine (ACh) signaling is fundamental to cocaine-induced changes in behavior and the striatal genomic response. We show that the D2R-dependent control of striatal ChIs enables the motor, sensitized, and reinforcing properties of cocaine. This study highlights the importance of the DA- and D2R-mediated inhibitory control of ChIs activity in the normal functioning of striatal networks.Entities:
Keywords: ChI-D2RKO mice; acetylcholine; addiction; cholingeric interneuron; cocaine; dopamine; dopamine D2 receptor; medium spiny neurons; reward; striatum
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Year: 2020 PMID: 32320647 DOI: 10.1016/j.celrep.2020.107527
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423