Published February 2005 | Version v1
Journal article

In vivo evaluation of [123I]-4-iodo-N-(4-(4-(2-methoxyphenyl)-piperazin-1-yl)butyl)-benzamide: a potential sigma receptor ligand for SPECT studies

  • 1. Department of Radiopharmacy, Faculty of Pharmaceutical Sciences, Gent University, Harelbekestraat 72, B-9000 Gent (Belgium)
  • 2. Department of Psychiatry, Columbia University, New York, NY 10032 (United States)
  • 3. Division of Nuclear Medicine, Gent University Hospital, De Pintelaan 185, B-9000 Gent (Belgium)

Description

In this study, in vivo evaluation in mice and rabbits of [123I]-4-iodo-N-(4-(4-(2-methoxyphenyl)-piperazin-1-yl)butyl)-benzamide ([123I]-BPB), a potential radioligand for visualisation of the sigma receptor by single photon emission computed tomography (SPECT), is reported. The compound possesses appropriate lipophilicity (log P=2.2) and binds sigma-1 and sigma-2 receptors (pKi=6.51 and 6.79, respectively). In mice, this new radioiodinated tracer exhibited high brain uptake (4.99% ID/g tissue at 10 min postinjection) and saturable binding (3.06% ID/g tissue at 10 min postinjection) as determined by pretreatment with unlabeled [123I]-BPB. A metabolite study demonstrated no (less than 5%) labeled metabolites in the brain. In rabbits, regional brain distribution was investigated and the tracer displayed high, homogeneous central nervous system uptake. Selectivity was assessed by competition experiments with known sigma ligands. Metabolite analysis showed no (less than 8%) labeled metabolites in the rabbit brain. In conclusion, our findings indicate that [123I]-BPB is not a suitable tracer for visualisation of D3 receptors while its potential for sigma receptor imaging is severely hampered by its affinity for dopamine receptors

Additional details

Identifiers

DOI
10.1016/j.nucmedbio.2004.09.007;
PII
S0969-8051(04)00170-2;

Publishing Information

Journal Title
Nuclear Medicine and Biology
Journal Volume
32
Journal Issue
2
Journal Page Range
p. 193-200
ISSN
0969-8051
CODEN
NMBIEO

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.