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Preclinical characterization of [18F]T-008, a novel PET imaging radioligand for cholesterol 24-hydroxylase.
- 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]
- Subjects :
- CHOLESTEROL
HYDROXYLASES
BRAIN enzymes
HOMEOSTASIS
SPASM treatment
EPILEPSY
Subjects
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