Glutamatergic neuroplasticity in cocaine addiction

Prog Mol Biol Transl Sci. 2011:98:367-400. doi: 10.1016/B978-0-12-385506-0.00009-0.

Abstract

Neuroadaptations among glutamatergic projections within the mesocorticolimbic circuits engaged by drugs of abuse have been described since the 1990s. There is now substantial evidence that drugs of abuse lead to long-term changes in glutamatergic signaling and encompass multiple levels of analysis. For example, cocaine induces changes in extracellular glutamate concentrations and in synaptic glutamatergic transmission. In addition, glutamate receptors are required for the expression of cocaine-related behaviors, and long-term changes have been reported in the expression of proteins at glutamatergic synapses, in glutamate-related redox regulation of neurons, and in glutamatergic synaptic and structural plasticity following chronic exposure to cocaine. In this chapter, we will describe the neurocircuitry involved, and will summarize evidence for adaptations in glutamatergic neuroplasticity as a mechanism for cocaine addiction. Finally, we will discuss progress in the development of glutamate-mediated pharmacotherapies for the treatment of cocaine dependence.

Publication types

  • Review

MeSH terms

  • Animals
  • Cocaine-Related Disorders / drug therapy
  • Cocaine-Related Disorders / metabolism
  • Cocaine-Related Disorders / physiopathology*
  • Glutamic Acid / metabolism*
  • Homeostasis
  • Humans
  • Nerve Net / physiopathology
  • Neuronal Plasticity*
  • Oxidation-Reduction

Substances

  • Glutamic Acid