The rate of cocaine administration alters gene regulation and behavioral plasticity: implications for addiction

J Neurosci. 2004 Jul 14;24(28):6362-70. doi: 10.1523/JNEUROSCI.1205-04.2004.

Abstract

The rapid delivery of drugs of abuse to the brain is thought to promote addiction, but why this occurs is unknown. In the present study, we characterized the influence of rate of intravenous cocaine infusion (5-100 sec) on three effects thought to contribute to its addiction liability: its ability to block dopamine (DA) uptake, to activate immediate early gene expression, and to produce psychomotor sensitization. Rapid infusions potentiated the ability of cocaine to block DA reuptake, to induce c-fos and arc mRNA expression, especially in mesocorticolimbic regions, and to produce psychomotor sensitization. Thus, the rate at which cocaine is delivered influences both its neurobiological impact and its ability to induce a form of drug experience-dependent plasticity implicated in addiction. We propose that rapidly delivered cocaine may be more addictive, in part, because this more readily induces forms of neurobehavioral plasticity that lead to the compulsive pursuit of drugs.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects*
  • Brain / drug effects*
  • Brain / metabolism
  • Cocaine / administration & dosage*
  • Cocaine / pharmacology
  • Cocaine / toxicity
  • Cocaine-Related Disorders / etiology*
  • Cytoskeletal Proteins
  • Dopamine / metabolism
  • Dopamine Uptake Inhibitors / administration & dosage
  • Dopamine Uptake Inhibitors / pharmacology
  • Dopamine Uptake Inhibitors / toxicity
  • Drug Administration Schedule
  • Frontal Lobe / drug effects
  • Frontal Lobe / metabolism
  • Gene Expression Regulation / drug effects*
  • Genes, Immediate-Early / drug effects
  • Genes, fos / drug effects
  • Immediate-Early Proteins / biosynthesis
  • Immediate-Early Proteins / genetics
  • In Situ Hybridization
  • Infusions, Intravenous
  • Limbic System / drug effects
  • Limbic System / metabolism
  • Locomotion / drug effects*
  • Male
  • Neostriatum / drug effects
  • Neostriatum / metabolism
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics
  • Nucleus Accumbens / drug effects
  • Nucleus Accumbens / metabolism
  • Prefrontal Cortex / drug effects
  • Prefrontal Cortex / metabolism
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-fos / genetics
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Cytoskeletal Proteins
  • Dopamine Uptake Inhibitors
  • Immediate-Early Proteins
  • Nerve Tissue Proteins
  • Proto-Oncogene Proteins c-fos
  • activity regulated cytoskeletal-associated protein
  • Cocaine
  • Dopamine