| Literature DB >> 25433637 |
Ping Su1, Shupeng Li1, Sheng Chen1, Tatiana V Lipina2, Min Wang1, Terence K Y Lai1, Frankie H F Lee1, Hailong Zhang1, Dongxu Zhai1, Stephen S G Ferguson3, José N Nobrega4, Albert H C Wong5, John C Roder2, Paul J Fletcher4, Fang Liu6.
Abstract
Current antipsychotic drugs primarily target dopamine D2 receptors (D2Rs), in conjunction with other receptors such as those for serotonin. However, these drugs have serious side effects such as extrapyramidal symptoms (EPS) and diabetes. Identifying a specific D2R signaling pathway that could be targeted for antipsychotic effects, without inducing EPS, would be a significant improvement in the treatment of schizophrenia. We report here that the D2R forms a protein complex with Disrupted in Schizophrenia 1 (DISC1) that facilitates D2R-mediated glycogen synthase kinase (GSK)-3 signaling and inhibits agonist-induced D2R internalization. D2R-DISC1 complex levels are increased in conjunction with decreased GSK-3α/β (Ser21/9) phosphorylation in both postmortem brain tissue from schizophrenia patients and in Disc1-L100P mutant mice, an animal model with behavioral abnormalities related to schizophrenia. Administration of an interfering peptide that disrupts the D2R-DISC1 complex successfully reverses behaviors relevant to schizophrenia but does not induce catalepsy, a strong predictor of EPS in humans.Entities:
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Year: 2014 PMID： 25433637 DOI： 10.1016/j.neuron.2014.11.007
Source DB: PubMed Journal: Neuron ISSN： 0896-6273 Impact factor: 17.173