Dynamic changes of striatal dopamine D 2 receptor binding at later stages after unilateral lesions of the medial forebrain bundle in Parkinsonian rat models

  • Wei Sun
  • , Kenji Sugiyama
  • , Tetsuya Asakawa
  • , Hiroshi Yamaguchi
  • , Soichi Akamine
  • , Yasuomi Ouchi
  • , Yasuhiro Magata
  • , Hiroki Namba

Research output: Contribution to journalArticlepeer-review

Abstract

Our previous study regarding the changes of D 2 receptor in nigrostriatal dopamine system at an early stage (4 weeks after lesion) indicated a different functional activity of striatal D 2 receptor between two different rat parkinsonian models, lesioning with 6-hydroxydopamine in the striatum and in the medial forebrain bundle (MFB). In the present study, we further examined binding of D 2 receptor as well as pre-synaptic dopamine transporter (DAT) at later stages (6 months after lesion) both in the striatal and MFB lesion models. The D 2 receptor binding in MFB model at 6 months after lesion was significantly lower than that at 4 weeks after lesion, albeit it was still higher than the normal side. The D 2 receptor binding in striatal model was decreased to the same extent at both 4 weeks and 6 months after lesion. DAT binding decreased at 6 months after lesion, more profound in MFB model, and the degree of reduction was not different from that at 4 weeks after lesion. These findings indicated different dynamic processes of the D 2 receptor and DAT during a longer time observation in the striatal and MFB lesion models. The dynamic changes of D 2 receptor activity after lesion should be considered when selecting 6-hydroxydopamine-induced rat parkinsonian models.

Original languageEnglish
Pages (from-to)157-162
Number of pages6
JournalNeuroscience Letters
Volume496
Issue number3
DOIs
Publication statusPublished - 08-06-2011
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General Neuroscience

Fingerprint

Dive into the research topics of 'Dynamic changes of striatal dopamine D 2 receptor binding at later stages after unilateral lesions of the medial forebrain bundle in Parkinsonian rat models'. Together they form a unique fingerprint.

Cite this