1986
DOI: 10.1016/0883-2889(86)90044-4
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Preparation of 11C-labelled SCH 23390 for the in vivo study of dopamine D-1 receptors using positron emission tomography

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Cited by 172 publications
(54 citation statements)
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“…In contrast to the non-reversible binding kinetics in the striatum observed with D 1 radiotracers such as SCH 23390 and NNC 756 (Halldin et al 1986;Farde et al 1987;Halldin et al 1993), [ 3 H]A69024 had a relatively rapid washout from the striatum, which is consistent with its lower affinity for D 1 receptors. This reversible binding profile suggests that A69024 may prove to be a preferable radiotracer over the currently used high affinity benzazepine radioligands for PET studies involving quantification of D 1 receptor densities.…”
Section: Discussionmentioning
confidence: 87%
“…In contrast to the non-reversible binding kinetics in the striatum observed with D 1 radiotracers such as SCH 23390 and NNC 756 (Halldin et al 1986;Farde et al 1987;Halldin et al 1993), [ 3 H]A69024 had a relatively rapid washout from the striatum, which is consistent with its lower affinity for D 1 receptors. This reversible binding profile suggests that A69024 may prove to be a preferable radiotracer over the currently used high affinity benzazepine radioligands for PET studies involving quantification of D 1 receptor densities.…”
Section: Discussionmentioning
confidence: 87%
“…11 C]SCH23390 (300 MBq) (Halldin et al, 1986) was injected into the left antecubital vein. A plaster helmet was made for each participant individually and used to fixate the head and minimize motion.…”
Section: Pet Datamentioning
confidence: 99%
“…The first PET radiotracer for the D 1 receptor to be introduced was the benzazepine [ 11 C]SCH 23390 (Halldin et al, 1986;Farde et al, 1987;Chipkin et al, 1988;Andersen et al, 1992). In vitro, SCH 23390 displayed only moderate D 1 to 5-HT 2A receptor selectivity (Laruelle et al, 1991).…”
Section: Introductionmentioning
confidence: 99%