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The role of the neuropeptide PEN receptor, GPR83, in the reward pathway: Relationship to sex-differences.
Fakira, Amanda K; Peck, Emily G; Liu, Yutong; Lueptow, Lindsay M; Trimbake, Nikita A; Han, Ming-Hu; Calipari, Erin S; Devi, Lakshmi A.
Afiliação
  • Fakira AK; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA.
  • Peck EG; Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Liu Y; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA; Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, NY, NY, USA.
  • Lueptow LM; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA.
  • Trimbake NA; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA.
  • Han MH; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA; Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, NY, NY, USA.
  • Calipari ES; Department of Pharmacology, Vanderbilt Center for Addiction Research, Vanderbilt Brain Institute, Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Devi LA; Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, NY, NY, USA; Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, NY, NY, USA. Electronic address: lakshmi.devi@mssm.edu.
Neuropharmacology ; 157: 107666, 2019 10.
Article em En | MEDLINE | ID: mdl-31199956
GPR83, the receptor for the neuropeptide PEN, exhibits high expression in the nucleus accumbens of the human and rodent brain, suggesting that it plays a role in modulating the mesolimbic reward pathway. However, the cell-type specific expression of GPR83, its functional impact in the reward pathway, and in drug reward-learning has not been fully explored. Using GPR83/eGFP mice, we show high GPR83 expression on cholinergic interneurons in the nucleus accumbens and moderate expression on ventral tegmental area dopamine neurons. In GPR83 knockout mice, baseline dopamine release in the nucleus accumbens is enhanced which disrupts the ratio of tonic vs phasic release. Additionally, GPR83 knockout leads to changes in the expression of dopamine-related genes. Using the morphine conditioned place preference model, we identify sex differences in morphine reward-learning, show that GPR83 is upregulated in the nucleus accumbens following morphine conditioned place preference, and show that shRNA-mediated knockdown of GPR83 in the nucleus accumbens leads to attenuation morphine reward. Together, these findings detect GPR83 expression in the reward-pathway, and show its involvement in dopamine release and morphine reward-learning.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Recompensa / Caracteres Sexuais / Receptores Acoplados a Proteínas G / Aprendizagem Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Recompensa / Caracteres Sexuais / Receptores Acoplados a Proteínas G / Aprendizagem Idioma: En Ano de publicação: 2019 Tipo de documento: Article