Striatal cell type-specific overexpression of DeltaFosB enhances incentive for cocaine

J Neurosci. 2003 Mar 15;23(6):2488-93. doi: 10.1523/JNEUROSCI.23-06-02488.2003.

Abstract

The transcription factor DeltaFosB accumulates in substance P-dynorphin-containing striatal neurons with repeated cocaine use. Here, we show that inducible transgenic DeltaFosB overexpression in this same striatal cell type facilitates acquisition of cocaine self-administration at low-threshold doses, consistent with increased sensitivity to the pharmacological effects of the drug. Importantly, DeltaFosB also enhances the degree of effort mice will exert to maintain self-administration of higher doses on a progressive ratio schedule of reinforcement, whereas levels of cocaine intake are not altered on less demanding fixed-ratio schedules. Acquisition and extinction of behavior reinforced by food pellets is not altered in DeltaFosB-overexpressing mice, indicating that DeltaFosB does not alter the capacity to learn an instrumental response or cause response perseveration in the absence of reinforcement. These data suggest that accumulation of DeltaFosB contributes to drug addiction by increasing the incentive properties of cocaine, an effect that could increase the risk for relapse long after cocaine use ceases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Cocaine / administration & dosage*
  • Cocaine-Related Disorders / physiopathology*
  • Corpus Striatum / cytology
  • Corpus Striatum / metabolism*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Doxycycline / pharmacology
  • Drug Administration Schedule
  • Dynorphins / biosynthesis
  • Gene Expression / drug effects
  • Mice
  • Mice, Transgenic
  • Motivation*
  • Neurons / drug effects
  • Neurons / metabolism
  • Organ Specificity
  • Proto-Oncogene Proteins c-fos / biosynthesis*
  • Proto-Oncogene Proteins c-fos / genetics
  • Reinforcement, Psychology
  • Self Administration
  • Substance P / biosynthesis
  • Transgenes / physiology

Substances

  • Proto-Oncogene Proteins c-fos
  • Substance P
  • Dynorphins
  • Cocaine
  • Doxycycline