Literature DB >> 29730825

18F-F13640 preclinical evaluation in rodent, cat and primate as a 5-HT1A receptor agonist for PET neuroimaging.

Benjamin Vidal1, Sylvain Fieux1, Matthieu Colom1, Thierry Billard2, Caroline Bouillot3, Olivier Barret4, Cristian Constantinescu4, Gilles Tamagnan4, Adrian Newman-Tancredi5, Luc Zimmer6,7.   

Abstract

Serotonin 1A receptors are known to play an important role in many psychiatric and neurodegenerative disorders. Currently, all available 5-HT1A receptor PET radiopharmaceuticals that are radiolabeled with fluorine-18 are antagonists. As agonists bind preferentially to the high-affinity state of receptors, it would be of great interest to develop agonist radioligands which could provide a measure of the functional 5-HT1A receptors in pathophysiological processes. The 5-HT1A receptor agonist candidates we recently proposed had promising in vitro properties but were not optimal in terms of PET imaging. F13640, a.k.a befiradol or NLX-112, is a 5-HT1A receptor agonist with a high affinity (Ki = 1 nM) and a high selectivity that would be suitable for a potential PET radiopharmaceutical. With propose here the first preclinical evaluation of 18F-F13640. 18F-F13640's nitro-precursor was synthesized and radiolabeled via a fluoro-nucleophilic substitution. Its radiopharmacological characterization included autoradiographic studies, metabolic studies, and in vivo PET scans in rat, cat and non-human primate. Some of the results were compared with the radiotracer 18F-MPPF, a 5-HT1A receptor antagonist. The radiochemical purity of 18F-F13640 was > 98%. In vitro binding pattern was consistent with the 5-HT1A receptor distribution. Metabolic studies revealed that the radiotracer rapidly entered the brain and led to few brain radiometabolites. Although 18F-F13640 in vivo binding was blocked by the 5-HT1A antagonist WAY-100635 and the 5-HT1A agonist 8-OH-DPAT, the distribution pattern was markedly different from antagonist radiotracers in the three species, suggesting it provides novel information on 5-HT1A receptors. Preliminary studies also suggest a high sensitivity of 18F-F13640 to endogenous serotonin release. 18F-F13640 has suitable characteristics for probing in vitro and in vivo the 5-HT1A receptors in high-affinity state. Quantification analyses with kinetic modeling are in progress to prepare the first-in-man study of 18F-F13640.

Entities:  

Keywords:  Agonist; Cat; PET tracer; Primate; Rat; Serotonin 1A receptor

Mesh:

Substances:

Year:  2018        PMID: 29730825     DOI: 10.1007/s00429-018-1672-7

Source DB:  PubMed          Journal:  Brain Struct Funct        ISSN: 1863-2653            Impact factor:   3.270


  8 in total

1.  18F-F13640 PET imaging of functional receptors in humans.

Authors:  Matthieu Colom; Nicolas Costes; Jérôme Redouté; Frédéric Dailler; Florent Gobert; Didier Le Bars; Thierry Billard; Adrian Newman-Tancredi; Luc Zimmer
Journal:  Eur J Nucl Med Mol Imaging       Date:  2019-08-14       Impact factor: 9.236

2.  Synthesis and evaluation of two new candidate high-affinity full agonist PET radioligands for imaging 5-HT1B receptors.

Authors:  Anton Lindberg; Shuiyu Lu; Sangram Nag; Magnus Schou; Jeih-San Liow; Sami S Zoghbi; Michael P Frankland; Robert L Gladding; Cheryl L Morse; Akihiro Takano; Nahid Amini; Charles S Elmore; Yong Sok Lee; Robert B Innis; Christer Halldin; Victor W Pike
Journal:  Nucl Med Biol       Date:  2019-01-26       Impact factor: 2.408

3.  Improvement of lower urinary tract function by a selective serotonin 5-HT1A receptor agonist, NLX-112, after chronic spinal cord injury.

Authors:  Ching-Yi Lin; Alexander Sparks; Yu-Shang Lee
Journal:  Exp Neurol       Date:  2020-06-30       Impact factor: 5.330

Review 4.  Radiotracers for the Central Serotoninergic System.

Authors:  Reynald Mangeant; Emmanuelle Dubost; Thomas Cailly; Valérie Collot
Journal:  Pharmaceuticals (Basel)       Date:  2022-05-03

5.  The selective 5-HT1A receptor agonist, NLX-112, exerts anti-dyskinetic and anti-parkinsonian-like effects in MPTP-treated marmosets.

Authors:  Ria Fisher; Atsuko Hikima; Rebecca Morris; Michael J Jackson; Sarah Rose; Mark A Varney; Ronan Depoortere; Adrian Newman-Tancredi
Journal:  Neuropharmacology       Date:  2020-02-10       Impact factor: 5.250

6.  [18F]F13640, a 5-HT1A Receptor Radiopharmaceutical Sensitive to Brain Serotonin Fluctuations.

Authors:  Matthieu Colom; Benjamin Vidal; Sylvain Fieux; Jérôme Redoute; Nicolas Costes; Franck Lavenne; Inés Mérida; Zacharie Irace; Thibaud Iecker; Caroline Bouillot; Thierry Billard; Adrian Newman-Tancredi; Luc Zimmer
Journal:  Front Neurosci       Date:  2021-03-08       Impact factor: 4.677

Review 7.  Towards in vivo imaging of functionally active 5-HT1A receptors in schizophrenia: concepts and challenges.

Authors:  Oriane Razakarivony; Adrian Newman-Tancredi; Luc Zimmer
Journal:  Transl Psychiatry       Date:  2021-01-07       Impact factor: 6.222

Review 8.  Hunting for the high-affinity state of G-protein-coupled receptors with agonist tracers: Theoretical and practical considerations for positron emission tomography imaging.

Authors:  Vladimir Shalgunov; Aren van Waarde; Jan Booij; Martin C Michel; Rudi A J O Dierckx; Philip H Elsinga
Journal:  Med Res Rev       Date:  2018-11-18       Impact factor: 12.944

  8 in total

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