| Literature DB >> 34506723 |
Sheng Gong1, Nicholas Fayette2, Jasper A Heinsbroek2, Christopher P Ford3.
Abstract
Cocaine addiction is a chronic, relapsing disorder characterized by maladaptation in the brain mesolimbic and nigrostriatal dopamine system. Although changes in the properties of D2-receptor-expressing medium spiny neurons (D2-MSNs) and connected striatal circuits following cocaine treatment are known, the contributions of altered D2-receptor (D2R) function in mediating the rewarding properties of cocaine remain unclear. Here, we describe how a 7-day exposure to cocaine alters dopamine signaling by selectively reducing the sensitivity, but not the expression, of nucleus accumbens D2-MSN D2Rs via an alteration in the relative expression and coupling of G protein subunits. This cocaine-induced reduction of D2R sensitivity facilitated the development of the rewarding effects of cocaine as blocking the reduction in G protein expression was sufficient to prevent cocaine-induced behavioral adaptations. These findings identify an initial maladaptive change in sensitivity by which mesolimbic dopamine signals are encoded by D2Rs following cocaine exposure.Entities:
Keywords: G protein; GPCR; addiction; basal ganglia; metabotropic; psychostimulant
Mesh:
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Year: 2021 PMID: 34506723 PMCID: PMC8571051 DOI: 10.1016/j.neuron.2021.08.012
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173