Abstract
1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-[(11)C]ethyl-1,3-dihydro-2H-benzimidazol-2-one ([(11)C]CPEB) was synthesized by [(11)C]N-ethylation and evaluated as a potential brain ORL1 receptor imaging agent by positron emission tomography. The uptake of [(11)C]CPEB in the mouse brain was 1.9% dose/g, 2 min post-injection, and gradually decreased with time. Receptor-specific binding was observed, however, the contribution of other receptors was observed and the non-specific binding of [(11)C]CPEB was too high for imaging receptors in vivo. Therefore, [(11)C]CPEB is not a suitable tracer for in vivo ORL1 receptor imaging.
Copyright 2002 Elsevier Science Inc.
Publication types
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Comparative Study
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Evaluation Study
MeSH terms
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Animals
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Benzimidazoles / chemical synthesis*
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Benzimidazoles / pharmacokinetics*
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Brain / diagnostic imaging*
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Brain / drug effects
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Brain / metabolism*
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Carbon Radioisotopes / chemistry
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Carbon Radioisotopes / pharmacokinetics
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Isotope Labeling / methods
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Male
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Metabolic Clearance Rate
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Mice
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Mice, Inbred Strains
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Nociceptin
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Nociceptin Receptor
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Opioid Peptides / pharmacology
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Organ Specificity
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Piperidines / chemical synthesis*
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Piperidines / pharmacokinetics*
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Radiopharmaceuticals / chemical synthesis
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Radiopharmaceuticals / pharmacokinetics
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Receptors, Opioid / metabolism*
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Reference Values
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Tissue Distribution
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Tomography, Emission-Computed / methods
Substances
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Benzimidazoles
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Carbon Radioisotopes
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J 113397
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Opioid Peptides
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Piperidines
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Radiopharmaceuticals
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Receptors, Opioid
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Nociceptin Receptor
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Oprl1 protein, mouse