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DISC1 signaling in cocaine addiction: Towards molecular mechanisms of co-morbidity

  • SUNY Buffalo
  • Johns Hopkins University

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Substance abuse and other psychiatric diseases may share molecular pathology. In order to test this hypothesis, we examined the role of Disrupted In Schizophrenia 1 (DISC1), a psychiatric risk factor, in cocaine self-administration (SA). Cocaine SA significantly increased expression of DISC1 in the nucleus accumbens (NAc); while knockdown of DISC1 in NAc significantly increased cocaine SA and decreased phosphorylation of GSK-3β at Ser9 compared to scrambled shRNA. Our study provides the first mechanistic evidence of a critical role of DISC1 in drug-induced behavioral neuroadaptations and sheds more light at the shared molecular pathology of drug abuse and other major psychiatric disorders.

Original languageEnglish
Pages (from-to)70-74
Number of pages5
JournalNeuroscience Research
Volume105
DOIs
StatePublished - Apr 1 2016

Keywords

  • Co-morbidity
  • Cocaine
  • DISC1
  • Drug abuse
  • Psychiatric disorders

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