000134641 001__ 134641 000134641 005__ 20250129092426.0 000134641 0247_ $$2doi$$a10.1007/s11307-013-0621-3 000134641 0247_ $$2pmid$$apmid:23456885 000134641 0247_ $$2ISSN$$a1536-1632 000134641 0247_ $$2ISSN$$a1860-2002 000134641 0247_ $$2WOS$$aWOS:000321972500013 000134641 037__ $$aFZJ-2013-02758 000134641 041__ $$aENG 000134641 082__ $$a610 000134641 1001_ $$0P:(DE-Juel1)131691$$aKroll, Tina$$b0$$eCorresponding author$$ufzj 000134641 245__ $$aSuitability of [18F]Altanserin and PET to Determine 5-HT2A Receptor Availability in the Rat Brain: In Vivo and In Vitro Validation of Invasive and Non-Invasive Kinetic Models 000134641 260__ $$aAmsterdam [u.a.]$$bElsevier Science$$c2013 000134641 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1378707244_1314 000134641 3367_ $$2DataCite$$aOutput Types/Journal article 000134641 3367_ $$00$$2EndNote$$aJournal Article 000134641 3367_ $$2BibTeX$$aARTICLE 000134641 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000134641 3367_ $$2DRIVER$$aarticle 000134641 500__ $$3POF3_Assignment on 2016-02-29 000134641 520__ $$aPURPOSE: While the selective 5-hydroxytryptamine type 2a receptor (5-HT2AR) radiotracer [(18)F]altanserin is well established in humans, the present study evaluated its suitability for quantifying cerebral 5-HT2ARs with positron emission tomography (PET) in albino rats. PROCEDURES: Ten Sprague Dawley rats underwent 180 min PET scans with arterial blood sampling. Reference tissue methods were evaluated on the basis of invasive kinetic models with metabolite-corrected arterial input functions. In vivo 5-HT2AR quantification with PET was validated by in vitro autoradiographic saturation experiments in the same animals. RESULT: Overall brain uptake of [(18)F]altanserin was reliably quantified by invasive and non-invasive models with the cerebellum as reference region shown by linear correlation of outcome parameters. Unlike in humans, no lipophilic metabolites occurred so that brain activity derived solely from parent compound. PET data correlated very well with in vitro autoradiographic data of the same animals. CONCLUSION: [(18)F]Altanserin PET is a reliable tool for in vivo quantification of 5-HT2AR availability in albino rats. Models based on both blood input and reference tissue describe radiotracer kinetics adequately. 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