INVIVO IMAGING OF MONOAMINERGIC NERVE-TERMINALS IN NORMAL AND MPTP-LESIONED PRIMATE BRAIN USING POSITRON EMISSION TOMOGRAPHY (PET) AND [C-11] TETRABENAZINE
Jn. Dasilva et al., INVIVO IMAGING OF MONOAMINERGIC NERVE-TERMINALS IN NORMAL AND MPTP-LESIONED PRIMATE BRAIN USING POSITRON EMISSION TOMOGRAPHY (PET) AND [C-11] TETRABENAZINE, Synapse, 14(2), 1993, pp. 128-131
The first successful in vivo imaging of monoamine vesicular transporte
rs in the living primate brain is described, using [C-11]tetrabenazine
([C-11]TBZ) and Positron Emission Tomography (PET). Radioligand uptak
e into brain is rapid, and at short time periods (10-30 minutes) the h
igher uptake and retention of the radiotracer in the more densely dopa
minergic innervated striatum is clearly visualized. Specific binding i
n striatum can be entirely blocked with co-administration of a pharmac
ological dose (1 mg/kg i.v.) of tetrabenazine. In a unilaterally MPTP-
lesioned monkey, specific binding of radioligand was absent in the, st
riatum on the lesioned side, with no effect on radiotracer distributio
n in the cortex, cerebellum or contralateral striatum. PET imaging wit
h [C-11]TBZ provides a new approach to the in vivo study of monoaminer
gic neurons and their loss in neurodegenerative diseases.