Signaling pathway adaptations and novel protein kinase A substrates related to behavioral sensitization to cocaine

Amy C. Boudreau, Carrie R. Ferrario, Marc J. Glucksman, Marina E. Wolf

Research output: Contribution to journalArticlepeer-review

73 Scopus citations


Behavioral sensitization is an animal model for aspects of cocaine addiction. Cocaine-sensitized rats exhibit increased AMPA receptor (AMPAR) surface expression in the nucleus accumbens (NAc) which may in turn enhance drug seeking. To identify signaling pathways contributing to AMPAR up-regulation, we measured AMPAR surface expression and signaling pathway activation in the NAc of cocaine-sensitized rats, cocaine-exposed rats that failed to sensitize and saline controls on withdrawal days (WD) 1, 7, and 21. We focused on calcium/calmodulin-dependent protein kinase II (CaMKII), extracellular signal-regulated protein kinase (ERK), and protein kinase A (PKA). In sensitized rats, AMPAR surface expression was elevated on WD7 and WD21 but not WD1. ERK2 activation followed a parallel time-course, suggesting a role in AMPAR up-regulation. Both sensitized and non-sensitized rats exhibited CaMKII activation on WD7, suggesting that CaMKII activation is not sufficient for AMPAR up-regulation. PKA phosphorylation, measured using an antibody recognizing phosphorylated PKA substrates, increased gradually over withdrawal in sensitized rats, from below control levels on WD1 to significantly greater than controls on WD21. Using proteomics, novel sensitization-related PKA substrates were identified, including two structural proteins (CRMP-2 and α-tubulin) that we speculate may link PKA signaling to previously reported dendritic remodeling in NAc neurons of cocaine-sensitized rats.

Original languageEnglish (US)
Pages (from-to)363-377
Number of pages15
JournalJournal of neurochemistry
Issue number1
StatePublished - Jul 2009
Externally publishedYes


  • AMPA receptor
  • Addiction
  • Cocaine
  • Nucleus accumbens
  • Rat
  • Receptor trafficking
  • Sensitization

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience


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