Time course changes of the striatum neuropil after unilateral dopamine depletion and the usefulness of the contralateral striatum as a control structure

Neurol Res. 2008 Dec;30(10):1068-74. doi: 10.1179/174313208X346116. Epub 2008 Sep 29.

Abstract

Introduction: After unilateral dopamine depletion, some ipsilateral alterations occur and the contralateral structure has been utilized as control.

Objective: Our aim is to analyse the evolution of the ultrastructural alterations of the ipsilateral and contralateral striata of the 6-hydroxydopamine lesioned rats to demonstrate that the contralateral striatum should not be used as control structure.

Methods: After the surgery and the rotation behavior evaluation, animals were killed from 3 to 120 days after lesioning, and their striata were compared with those of aged rats.

Results: The ultrastructural analysis shows increased diameter of the synaptic ending in ipsilateral (since the third day) and contralateral striata (since day 30) and an increase in perforated synaptic contacts.

Conclusion: Our data suggest that the contralateral striatum should not be taken as control structure at least after 20-30 days after lesioning, as the alterations found here may result in wrong interpretations when comparing with the ipsilateral-lesioned one.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Agents
  • Animals
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Corpus Striatum / ultrastructure
  • Disease Models, Animal
  • Dopamine / metabolism*
  • Functional Laterality / drug effects
  • Functional Laterality / physiology*
  • Male
  • Microscopy, Electron, Transmission / methods
  • Neuropil / pathology*
  • Neuropil / ultrastructure
  • Neurotoxicity Syndromes / etiology
  • Neurotoxicity Syndromes / metabolism*
  • Neurotoxicity Syndromes / pathology*
  • Neurotoxicity Syndromes / physiopathology*
  • Oxidopamine / toxicity
  • Rats
  • Rats, Wistar
  • Synapses / drug effects
  • Synapses / ultrastructure
  • Time Factors

Substances

  • Adrenergic Agents
  • Oxidopamine
  • Dopamine