Estimation of D2-like receptor occupancy by dopamine in the putamen of hemiparkinsonian monkeys

Svetlana I. Chefer, Alane S. Kimes, John A. Matochik, Andrew G. Horti, Varughese Kurian, Dean Shumway, Edward F. Domino, Edythe D. London, Alexey G. Mukhin

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


To advance understanding of the neurochemical changes in Parkinson's disease (PD), we compared D2-like dopamine receptor occupancy by dopamine in the control and lesioned putamen of four pig-tailed macaques treated unilaterally with MPTP. PET and in vitro binding techniques were used to measure binding potential (BP*) and density of D2-like dopamine receptors (B max), respectively. As would be expected in PD, relatively higher values of BP* and Bmax and less amphetamine-induced decrease in [11C]raclopride binding were observed in the lesioned compared with the contralateral putamen in each animal. The percent differences between lesioned and contralateral sides were similar whether the measurements were of [11C]raclopride BP* or Bmax values, measured in vivo and in vitro, respectively. As [11C]raclopride BP* is a measure of the density of D2-like dopamine receptors available for radioligand binding (i.e., not occupied by dopamine), these findings suggest that the fractional occupancy of receptors by endogenous dopamine in the lesioned putamen is nearly equal to that in the contralateral putamen. Therefore, the absolute number of receptors occupied by dopamine, which is a product of receptor density and fractional occupancy by dopamine, is greater in the lesioned than in the contralateral putamen. One possible explanation for the lack of differences in fractional occupancy of D2 receptors by dopamine (despite a loss in available dopamine) is a lesion-induced increase in a portion of low-affinity D2 receptors to a state of high affinity for dopamine.

Original languageEnglish (US)
Pages (from-to)270-278
Number of pages9
Issue number2
StatePublished - Jan 2008


  • MPTP model of PD
  • PET
  • Striatum
  • [C]raclopride

ASJC Scopus subject areas

  • Pharmacology
  • Psychiatry and Mental health


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