Chronic morphine induces visible changes in the morphology of mesolimbic dopamine neurons

Liora Sklair-Tavron, Wei Xing Shi, Sarah B. Lane, Herbert W. Harris, Benjamin S. Bunney, Eric J. Nestler

Research output: Contribution to journalArticlepeer-review

262 Scopus citations

Abstract

The mesolimbic dopamine system, which arises in the ventral tegmental area (VTA), is an important neural substrate for opiate reinforcement and addiction. Chronic exposure to opiates is known to produce biochemical adaptations in this brain region. We now show that these adaptations are associated with structural changes in VTA dopamine neurons. Individual VTA neurons in paraformaldehyde-fixed brain sections from control or morphine- treated rats were injected with the fluorescent dye Lucifer yellow. The identity of the injected cells as dopaminergic or nondopaminergie was determined by immunnhistochemical labeling of the sections for tyrosine hydroxylase. Chronic morphine treatment resulted in a mean ≃25% reduction in the area and perimeter of VTA dopamine neurons. This reduction in cell size was prevented by concomitant treatment of rats with naltrexone, an opioid receptor antagonist, as well as by intra-VTA infusion of brain-derived neurotrophic factor. In contrast, chronic morphine treatment did not alter the size of nondopaminergic neurons in the VTA, nor did it affect the total number of dopaminergic neurons in this brain region. The results of these studies provide direct evidence for structural alterations in VTA dopamine neurons as a consequence of chronic opiate exposure, which could contribute to changes in mesolimbic dopamine function associated with addiction.

Original languageEnglish
Pages (from-to)11202-11207
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume93
Issue number20
DOIs
StatePublished - 1 Oct 1996
Externally publishedYes

Keywords

  • Lucifer yellow
  • brain-derived neurotrophic factor
  • mesolimbic dopamine system
  • opiate addiction
  • tyrosine hydroxylase

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