| First Author | Huang B | Year | 2018 |
| Journal | Sci Signal | Volume | 11 |
| Issue | 512 | PubMed ID | 29317519 |
| Mgi Jnum | J:272666 | Mgi Id | MGI:6285000 |
| Doi | 10.1126/scisignal.aam5402 | Citation | Huang B, et al. (2018) beta-Arrestin-biased beta-adrenergic signaling promotes extinction learning of cocaine reward memory. Sci Signal 11(512) |
| abstractText | Extinction learning of cocaine-associated contextual cues can help prevent cocaine addicts from relapsing. Pharmacological manipulation of beta-adrenergic receptor (beta-AR) during extinction learning is being developed as a potential strategy to treat drug addiction. We demonstrated that the extinction learning of cocaine-associated memory was mediated by beta-arrestin2-biased but not heterotrimeric guanine nucleotide-binding protein (G protein)-dependent beta-adrenergic signaling. We found that administration of the nonbiased beta-AR antagonist propranolol, but not the G protein-biased beta-AR antagonist carvedilol, blocked extinction learning of cocaine-conditioned place preference and the associated ERK activation in the infralimbic prefrontal cortex. Overexpression of beta-arrestin2 in the infralimbic prefrontal cortex promoted extinction learning, which was blocked by propranolol. Knockout of beta-arrestin2 in the infralimbic prefrontal cortex, specifically in excitatory neurons, impaired extinction learning of cocaine-conditioned place preference, which was not rescued by carvedilol. beta-Arrestin2 signaling in infralimbic excitatory neurons was also required for the extinction learning in the cocaine self-administration model. Our results suggest that beta-arrestin-biased beta-adrenergic signaling in the infralimbic prefrontal cortex regulates extinction learning of cocaine-associated memories and could be therapeutically targeted to treat addiction. |
