Literature DB >> 26917190

In vivo evaluation of [11C]preladenant positron emission tomography for quantification of adenosine A2A receptors in the rat brain.

Xiaoyun Zhou1, Shivashankar Khanapur1, Johan R de Jong1, Antoon Tm Willemsen1, Rudi Ajo Dierckx1, Philip H Elsinga1, Erik Fj de Vries1.   

Abstract

[11C]Preladenant was developed as a novel adenosine A2A receptor positron emission tomography radioligand. The present study aims to evaluate the suitability of [11C]preladenant positron emission tomography for the quantification of striatal A2A receptor density and the assessment of striatal A2A receptor occupancy by KW-6002. Sixty- or ninety-minute dynamic positron emission tomography imaging was performed on rats. Tracer kinetics was quantified by the two-tissue compartment model, Logan graphical analysis and several reference tissue-based models. Test-retest reproducibility was assessed by repeated imaging on two consecutive days. Two-tissue compartment model and Logan plot estimated comparable distribution volume ( VT) values of ∼10 in the A2A receptor-rich striatum and substantially lower values in all extra-striatal regions (∼1.5-2.5). The simplified reference tissue model with midbrain or occipital cortex as the reference region proved to be the best non-invasive model for quantification of A2A receptor, showing a striatal binding potential ( BPND) value of ∼5.5, and a test-retest variability of ∼5.5%. The brain metabolite analysis showed that at 60-min post injection, 17% of the radioactivity in the brain was due to radioactive metabolites. The ED50 of KW-6002 in rat striatum for i.p. injection was 0.044-0.062 mg/kg. The study demonstrates that [11C]preladenant is a suitable tracer to quantify striatal A2A receptor density and assess A2A receptor occupancy by A2A receptor-targeting molecules.

Entities:  

Keywords:  Adenosine A2A receptors; [11C]preladenant; pharmacokinetic modeling; receptor occupancy; small-animal positron emission tomography

Mesh:

Substances:

Year:  2016        PMID: 26917190      PMCID: PMC5381452          DOI: 10.1177/0271678X16634714

Source DB:  PubMed          Journal:  J Cereb Blood Flow Metab        ISSN: 0271-678X            Impact factor:   6.200


  39 in total

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Review 3.  Consensus nomenclature for in vivo imaging of reversibly binding radioligands.

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Journal:  J Cereb Blood Flow Metab       Date:  2007-05-09       Impact factor: 6.200

4.  Development of [18F]-labeled pyrazolo[4,3-e]-1,2,4- triazolo[1,5-c]pyrimidine (SCH442416) analogs for the imaging of cerebral adenosine A2A receptors with positron emission tomography.

Authors:  Shivashankar Khanapur; Soumen Paul; Anup Shah; Suresh Vatakuti; Michel J B Koole; Rolf Zijlma; Rudi A J O Dierckx; Gert Luurtsema; Prabha Garg; Aren van Waarde; Philip H Elsinga
Journal:  J Med Chem       Date:  2014-08-04       Impact factor: 7.446

5.  Synthesis and preclinical evaluation of 2-(2-furanyl)-7-[2-[4-[4-(2-[11C]methoxyethoxy)phenyl]-1-piperazinyl]ethyl]7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine-5-amine ([11C]Preladenant) as a PET tracer for the imaging of cerebral adenosine A2A receptors.

Authors:  Xiaoyun Zhou; Shivashankar Khanapur; Anja P Huizing; Rolf Zijlma; Marianne Schepers; Rudi A J O Dierckx; Aren van Waarde; Erik F J de Vries; Philip H Elsinga
Journal:  J Med Chem       Date:  2014-10-15       Impact factor: 7.446

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9.  Adenosine 2A receptor availability in dyskinetic and nondyskinetic patients with Parkinson disease.

Authors:  A F Ramlackhansingh; S K Bose; I Ahmed; F E Turkheimer; N Pavese; D J Brooks
Journal:  Neurology       Date:  2011-05-24       Impact factor: 9.910

10.  Test-retest variability of adenosine A2A binding in the human brain with (11)C-TMSX and PET.

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Journal:  EJNMMI Res       Date:  2014-12-29       Impact factor: 3.138

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Review 6.  Allosteric Interactions between Adenosine A2A and Dopamine D2 Receptors in Heteromeric Complexes: Biochemical and Pharmacological Characteristics, and Opportunities for PET Imaging.

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Review 7.  In Vivo PET Imaging of Adenosine 2A Receptors in Neuroinflammatory and Neurodegenerative Disease.

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