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Preclinical characterization of [18F]T-008, a novel PET imaging radioligand for cholesterol 24-hydroxylase.

Authors :
Koike, Tatsuki
Constantinescu, Cristian C.
Ikeda, Shuhei
Nishi, Toshiya
Sunahara, Eiji
Miyamoto, Maki
Cole, Patricia
Barret, Olivier
Alagille, David
Papin, Caroline
Morley, Thomas
Fowles, Krista
Seibyl, John
Tamagnan, Gilles
Kuroita, Takanobu
Source :
European Journal of Nuclear Medicine & Molecular Imaging; Mar2022, Vol. 49 Issue 4, p1148-1156, 9p, 1 Color Photograph, 2 Charts, 4 Graphs
Publication Year :
2022

Abstract

Purpose: Cholesterol 24-hydroxylase (CH24H) is a brain-specific enzyme that plays a major role in brain cholesterol homeostasis by converting cholesterol into 24S-hydroxycholesterol. The selective CH24H inhibitor soticlestat (TAK-935) is being pursued as a drug for treatment of seizures in developmental and epileptic encephalopathies. Herein, we describe the successful discovery and the preclinical validation of the novel radiolabeled CH24H ligand (3-[<superscript>18</superscript>F]fluoroazetidin-1-yl){1-[4-(4-fluorophenyl)pyrimidin-5-yl]piperidin-4-yl}methanone ([<superscript>18</superscript>F]T-008) and its tritiated analog, [<superscript>3</superscript>H]T-008. Methods: In vitro autoradiography (ARG) studies in the CH24H wild-type (WT) and knockout (KO) mouse brain sections were conducted using [<superscript>3</superscript>H]T-008. PET imaging was conducted in two adult rhesus macaques using [<superscript>18</superscript>F]T-008. Each macaque received two test–retest baseline scans and a series of two blocking doses of soticlestat administered prior to [<superscript>18</superscript>F]T-008 to determine the CH24H enzyme occupancy. PET data were analyzed with Logan graphical analysis using plasma input. A Lassen plot was applied to estimate CH24H enzyme occupancy by soticlestat. Results: In ARG studies, binding of [<superscript>3</superscript>H]T-008 was specific to CH24H in the mouse brain sections, which was not observed in CH24H KO or in wild-type mice after pretreatment with soticlestat. In rhesus PET studies, the rank order of [<superscript>18</superscript>F]T-008 uptake was striatum > cortical regions > cerebellum, which was consistent with CH24H distribution in the brain. Pre-blocking with soticlestat reduced the maximum uptake and increased the washout in all brain regions in a dose-dependent manner. Calculated global occupancy values for soticlestat at a dose of 0.89 mg/kg were 97–98%, indicating maximum occupancy. Conclusion: The preclinical in vitro and in vivo evaluation of labeled T-008 demonstrates that [<superscript>18</superscript>F]T-008 is suitable for imaging CH24H in the brain and warrants further studies in humans. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16197070
Volume :
49
Issue :
4
Database :
Complementary Index
Journal :
European Journal of Nuclear Medicine & Molecular Imaging
Publication Type :
Academic Journal
Accession number :
156400547
Full Text :
https://doi.org/10.1007/s00259-021-05565-z