학술논문

Radioiodinated SB 207710 as a radioligand in vivo: imaging of brain 5-HT[sub 4] receptors with SPET.
Document Type
Article
Source
European Journal of Nuclear Medicine & Molecular Imaging. 2003, Vol. 30 Issue 11, p1520. 9p.
Subject
*POSITRON emission tomography
*MEDICAL imaging systems
*RADIOLIGAND assay
*NEUROTRANSMITTER receptors
*CEREBELLUM
Language
ISSN
1619-7070
Abstract
Single-photon emission tomography (SPET) and positron emission tomography (PET), when coupled to suitable radioligands, are uniquely powerful for investigating the status of neurotransmitter receptors in vivo. The serotonin subtype-4 (5-HT[sub 4]) receptor has discrete and very similar distributions in rodent and primate brain. This receptor population may play a role in normal cognition and memory and is perhaps perturbed in some neuropsychiatric disorders. SB 207710 [(1-butyl-4-piperidinylmethyl)-8-amino-7-iodo-1,4-benzodioxan-5-carboxylate] is a selective high-affinity antagonist at 5-HT[sub 4] receptors. We explored radioiodinated SB 207710 as a possible radioligand for imaging 5-HT[sub 4] receptors in vivo. Rats were injected intravenously with iodine-125 labelled SB 207710, euthanised at known times and dissected to establish radioactivity content in brain tissues. Radioactivity entered brain but cleared rapidly and to a high extent from blood and plasma. Between 45 and 75 min after injection, the ratios of radioactivity concentration in each of 12 selected brain tissues to that in receptor-poor cerebellum correlated with previous measures of 5-HT[sub 4] receptor density distribution in vitro. The highest ratio was about 3.4 in striatum. SB 207710 was labelled with iodine-123 by an iododestannylation procedure. A cynomolgus monkey was injected intravenously with [[sup 123]I]SB 207710 and examined by SPET. Maximal whole brain uptake of radioactivity was 2.3% of the injected dose at 18 min after radioligand injection. Brain images acquired between 9 and 90 min showed high radioactivity uptake in 5-HT[sub 4] receptor-rich regions, such as striatum, and low uptake in receptor-poor cerebellum. At 169 min the ratio of radioactivity concentration in striatum to that in cerebellum was 4.0. In a second SPET experiment, the cynomolgus monkey was pretreated with a selective 5-HT[sub 4] receptor antagonist, SB 204070, at 20 min before [[sup 123]I]SB 207710 injection. Radioactivity in all brain regions was reduced almost to the level in cerebellum by 176 min after radioligand injection. These findings show that [[sup 123]I]SB 207710 is an effective radioligand for imaging brain 5-HT[sub 4] receptors in vivo. [ABSTRACT FROM AUTHOR]