
Activation of Protein Kinases and Phosphatases Coupled to Glutamate Receptors Regulates the Phosphorylation State of DARPP32 at Threonine 75 After Repeated Exposure to Cocaine in the Rat Dorsal Striatum in a Ca2+-Dependent Manner
Author(s) -
Jieun Kim,
In Soo Ryu,
Seungwan Seo,
Eun Sang Choe
Publication year - 2015
Publication title -
international journal of neuropsychopharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 107
eISSN - 1469-5111
pISSN - 1461-1457
DOI - 10.1093/ijnp/pyv075
Subject(s) - phosphorylation , kinase , phosphatase , glutamate receptor , protein kinase a , protein phosphorylation , protein kinase c , microbiology and biotechnology , synaptic plasticity , protein phosphatase 1 , chemistry , striatum , mitogen activated protein kinase , biology , biochemistry , dopamine , receptor , neuroscience
Phosphorylation state of dopamine- and cAMP-regulated phosphoprotein, molecular weight 32 kDa (DARPP32) is crucial to understand drug-mediated synaptic plasticity. In this study, mechanisms underlying repeated cocaine-stimulated phosphorylation of DARPP32 at threonine 75 (pDARPP32-Thr75) were determined by investigating the hypothesis that activation of protein kinases and phosphatases coupled to glutamate signaling is necessary for the regulation of pDARPP32-Thr75 after repeated cocaine administration.