کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2153978 1090215 2012 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Difficulties in dopamine transporter radioligand PET analysis: the example of LBT-999 using [18F] and [11C] labelling : Part I: PET studies
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
پیش نمایش صفحه اول مقاله
Difficulties in dopamine transporter radioligand PET analysis: the example of LBT-999 using [18F] and [11C] labelling : Part I: PET studies
چکیده انگلیسی

BackgroundLBT-999 (E)-N-(4-fluorobut-2-enyl)-2β-carbomethoxy-3β-(4′-tolyl)nortropane is a dopamine transporter (DAT) ligand. [18F]LBT-999 was first labelled with carbon-11; we will now describe its in vivo behaviour in comparison to that of [11C]LBT-999.Methods/ResultsPositron emission tomography (PET) experiments (baboons) confirmed the high affinity/specificity of [18F]LBT-999 for DAT. The brain regional distribution was in accordance with that of DAT. Pre-treatment with LBT-999 (1 mg/kg iv), but not with desipramine, a norepinephrine (NET) antagonist, reduced the striatum-to-cerebellum ratio by 96%, confirming the specificity for DAT vs. NET. The parent compound decreased rapidly and represented 24.3±5.0% of plasma radioactivity at 30 min pi. Whole-body scans showed an important bone uptake of free fluorine following metabolism of [18F]LBT-999. In the cerebellum and striatum, distribution volumes increased by 30–40% between 80 and 230 min, suggesting the polluting role of a radiometabolite(s). [11C]LBT-999 exhibited a 40% higher standardized uptake value in the striata. This difference is likely due to N-dealkylation followed by [18F]fluoride release. 2β-Carbomethoxy-3β-(4′-tolyl) nortropane is then formed, while [11C]2β-carbomethoxy-3β-(4′-tolyl) nortropane is formed following injection of [11C]LBT-999. This metabolite has high affinity for the DAT. In one specific PET experiment, intravenous injection of this metabolite induced a strong displacement of [18F]LBT-999 in the striata, confirming that this metabolite readily crosses the blood–brain barrier (BBB) and binds to DAT.Conclusions[18F]LBT-999 is N-dealkylated in vivo to yield (1) a nonradioactive metabolite that crosses the BBB and has a high affinity for the DAT and (2) a [18F]fluoro-alkyl chain which is further defluorinated. The temporal changes in distribution volumes are consistent with the accumulation of a radiometabolite(s) in the brain. Therefore, the quantification of DAT density with [18F]LBT-999 is rather difficult.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Nuclear Medicine and Biology - Volume 39, Issue 2, February 2012, Pages 227–233
نویسندگان
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