Intra-nigral MPTP lesion in rats: behavioral and autoradiography studies

Exp Neurol. 2005 Oct;195(2):322-9. doi: 10.1016/j.expneurol.2005.05.009.

Abstract

The present study investigated the motor response and possible changes in binding to D1 and D2 receptors after intra-nigral 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) infusion on rats. The results indicated that MPTP-lesioned rats exhibited a significant reduction in locomotion and rearing frequencies observed in an open field 24 h after surgery. However, at 7 and 14 days after surgery the MPTP-lesioned rats showed a significant increase in locomotion in comparison to the control groups, as well as a decrease in immobility time. In addition, 21 days after surgery the behavioral measurements were unaltered by these procedures. Moreover, latency in initiating movement and catalepsy were unchanged by this neurotoxin on the same days of observation. An autoradiography approach indicated that there was a reduction in [3H]SCH 23390 binding in substantia nigra pars compacta (SNpc), substantia nigra pars reticulata (SNpr) and ventrolateral striatum in MPTP-treated rats 21 days after the surgery. [3H]raclopride binding remained unaltered by the MPTP treatment. These results suggest that compensatory plastic changes occur in D1 dopamine receptors after partial lesion of nigral dopaminergic neurons. These alterations might be related to the occurrence and recovery of motor impairment observed in MPTP-lesioned rats.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Autoradiography*
  • Behavior, Animal / drug effects*
  • Benzazepines / pharmacokinetics
  • Catalepsy / physiopathology
  • Dopamine Antagonists / pharmacokinetics
  • Exploratory Behavior / drug effects
  • MPTP Poisoning / diagnostic imaging*
  • MPTP Poisoning / physiopathology
  • Male
  • Motor Activity / drug effects
  • Motor Activity / physiology
  • Radiography
  • Rats
  • Rats, Wistar
  • Statistics, Nonparametric
  • Substantia Nigra / diagnostic imaging*
  • Substantia Nigra / pathology
  • Time Factors
  • Tritium / pharmacokinetics

Substances

  • Benzazepines
  • Dopamine Antagonists
  • Tritium