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Journal of Neuroscience, Vol 12, 3773-3780, Copyright © 1992 by Society for Neuroscience
GABAergic inhibition of endogenous dopamine release measured in vivo with 11C-raclopride and positron emission tomography
SL Dewey, GS Smith, J Logan, JD Brodie, DW Yu, RA Ferrieri, PT King, RR MacGregor, TP Martin and AP Wolf
Department of Chemistry, Brookhaven National Laboratory, Upton, New York 11973.
Extensive neuroanatomical, neurophysiological, and behavioral evidence
demonstrates that GABAergic neurons inhibit endogenous dopamine release in
the mammalian corpus striatum. Positron emission tomography (PET) studies
in adult female baboons, using the dopamine D2-specific radiotracer
11C-raclopride, were undertaken to assess the utility of this imaging
technique for measuring these dynamic interactions in vivo. 11C-raclopride
binding was imaged prior to and following the administration of either
gamma-vinyl-GABA (GVG), a specific suicide inhibitor of the
GABA-catabolizing enzyme GABA transaminase, or lorazepam, a clinically
prescribed benzodiazepine agonist. Striatal 11C- raclopride binding
increased following both GVG and lorazepam administration. This increase
exceeded the test/retest variability of 11C-raclopride binding observed in
the same animals. These findings confirm that changes in endogenous
dopamine concentrations resulting from drug-induced potentiation of
GABAergic transmission can be measured with PET and 11C-raclopride.
Finally, this new strategy for noninvasively evaluating the functional
integrity of neurophysiologically linked transmitter systems with PET
supports its use as an approach for assessing the multiple mechanisms of
drug action and their consequences in the human brain.
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