Chronic cocaine administration modulates the expression of transcription factors involved in midbrain dopaminergic neuron function

Exp Neurol. 2007 Feb;203(2):472-80. doi: 10.1016/j.expneurol.2006.08.024. Epub 2006 Oct 27.

Abstract

Chronic cocaine use leads to pronounced alterations in neuronal functions in brain circuits associated with reward. In the present study, we examined in the rat midbrain the effects of acute, subchronic (5 days) and chronic cocaine treatments (14 days) on the gene expression of transcription factors involved in the development and maintenance of dopaminergic neurons. We show that chronic, but not acute or subchronic, cocaine administration downregulates Nurr1 and Pitx3 transcripts whereas En1 transcripts are upregulated. Conversely, Lmx1b and En2 transcripts are not affected by the drug treatment, indicating that the modulation of the midbrain transcription factors analyzed is highly selective. Interestingly, modification of the gene expression for these transcription factors persists in midbrain as long as two weeks after the last drug administration, suggesting that it may account for some of the enduring alterations in midbrain dopaminergic circuits associated with chronic cocaine use.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cocaine / administration & dosage
  • Cocaine / pharmacology*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics
  • Dopamine / physiology*
  • Dopamine Uptake Inhibitors / administration & dosage
  • Dopamine Uptake Inhibitors / pharmacology*
  • Homeodomain Proteins / biosynthesis
  • Homeodomain Proteins / genetics
  • Immunohistochemistry
  • LIM-Homeodomain Proteins
  • Male
  • Mesencephalon / cytology*
  • Mesencephalon / physiology*
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics
  • Neurons / drug effects
  • Neurons / physiology*
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • DNA-Binding Proteins
  • Dopamine Uptake Inhibitors
  • Homeodomain Proteins
  • LIM homeobox transcription factor 1 beta
  • LIM-Homeodomain Proteins
  • Nerve Tissue Proteins
  • Nr4a2 protein, rat
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • RNA, Messenger
  • Transcription Factors
  • engrailed 2 protein
  • homeobox protein PITX3
  • Tyrosine 3-Monooxygenase
  • Cocaine
  • Dopamine