Estimation of D2-like Receptor Occupancy by Dopamine in the Putamen of Hemiparkinsonian Monkeys
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...
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Veröffentlicht in: | Neuropsychopharmacology (New York, N.Y.) N.Y.), 2008-01, Vol.33 (2), p.270-278 |
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Sprache: | eng |
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Zusammenfassung: | 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
B
max
and less amphetamine-induced decrease in [
11
C]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 [
11
C]raclopride BP
*
or
B
max
values, measured
in vivo
and
in vitro
, respectively. As [
11
C]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. |
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ISSN: | 0893-133X 1740-634X |
DOI: | 10.1038/sj.npp.1301404 |