Acute cocaine exposure alters spine density and long-term potentiation in the ventral tegmental area

Eur J Neurosci. 2007 Aug;26(3):749-56. doi: 10.1111/j.1460-9568.2007.05689.x.

Abstract

Growing evidence indicates that the expression of synaptic plasticity in the central nervous system results in dendritic reorganization and spine remodeling. Although long-term potentiation of glutamatergic synapses after cocaine exposure in the ventral tegmental area (VTA) has been proposed as a cellular mechanism underlying addictive behaviors, the relationship between long-term potentiation and dendritic remodeling induced by cocaine on the dopaminergic neurons of the VTA has not been demonstrated. Here we report that rat VTA cells classified as type I and II showed distinct morphological responses to cocaine, as a single cocaine exposure significantly increased dendritic spine density in type I but not in type II cells. Further, only type I cells had a significant increase in the AMPA receptor:NMDA receptor ratio after a single cocaine exposure. Taken together, our data provide evidence that increased spine density and synaptic plasticity are coexpressed within the same VTA neuronal population and that only type I neurons are structurally and synaptically modified by cocaine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Cell Shape / drug effects
  • Cocaine / pharmacology*
  • Cocaine-Related Disorders / pathology
  • Cocaine-Related Disorders / physiopathology*
  • Dendritic Spines / drug effects*
  • Dendritic Spines / pathology
  • Dopamine / metabolism
  • Dopamine Uptake Inhibitors / pharmacology
  • Glutamic Acid / metabolism
  • Long-Term Potentiation / drug effects*
  • Lysine / analogs & derivatives
  • Male
  • Organ Culture Techniques
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, AMPA / drug effects
  • Receptors, AMPA / metabolism
  • Receptors, N-Methyl-D-Aspartate / drug effects
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Staining and Labeling
  • Synapses / drug effects
  • Synapses / pathology
  • Synaptic Transmission / drug effects
  • Ventral Tegmental Area / drug effects*
  • Ventral Tegmental Area / pathology
  • Ventral Tegmental Area / physiopathology*

Substances

  • Dopamine Uptake Inhibitors
  • Receptors, AMPA
  • Receptors, N-Methyl-D-Aspartate
  • Glutamic Acid
  • biocytin
  • Cocaine
  • Lysine
  • Dopamine