Cocaine experience establishes control of midbrain glutamate and dopamine by corticotropin-releasing factor: a role in stress-induced relapse to drug seeking

J Neurosci. 2005 Jun 1;25(22):5389-96. doi: 10.1523/JNEUROSCI.0955-05.2005.

Abstract

Footshock stress can reinstate cocaine-seeking behavior through a central action of the stress-associated neurohormone corticotropin-releasing factor (CRF). Here we report (1) that footshock stress releases CRF in the ventral tegmental area (VTA) of the rat brain, (2) that, in cocaine-experienced but not in cocaine-naive rats, this CRF acquires control over local glutamate release, (3) that CRF-induced glutamate release activates the mesocorticolimbic dopamine system, and (4) that, through this circuitry, footshock stress triggers relapse to drug seeking in cocaine-experienced animals. Thus, a long-lasting cocaine-induced neuroadaptation, presumably at the level of glutamate terminals in the VTA, appears to play an important role in stress-induced relapse to drug use. Similar neuroadaptations may be important for the comorbidity between addiction and other stress-related psychiatric disorders.

MeSH terms

  • Animals
  • Cocaine-Related Disorders / etiology
  • Cocaine-Related Disorders / metabolism*
  • Corticotropin-Releasing Hormone / pharmacology
  • Corticotropin-Releasing Hormone / physiology*
  • Dopamine / metabolism*
  • Glutamic Acid / metabolism*
  • Male
  • Microdialysis
  • Rats
  • Rats, Long-Evans
  • Recurrence
  • Stress, Physiological / complications*
  • Ventral Tegmental Area / metabolism*

Substances

  • Glutamic Acid
  • Corticotropin-Releasing Hormone
  • Dopamine