PET ligands [ 18 F]LSN3316612 and [ 11 C]LSN3316612 quantify O -linked-β- N -acetyl-glucosamine hydrolase in the brain

Autor: Peter J. Lindsay-Scott, Victor W. Pike, J. Craig Ruble, Maria Cuadrado, Mohammad B. Haskali, Michael P. Johnson, Susan DuBois, Nancy Kant, Hugh Nuthall, Shuiyu Lu, Jeremy Gilmore, Kevin Michael Ruley, Aneta Kowalski, Enrique Jambrina, S Michelle Morin, Adrian J. Mogg, Soumen Paul, Andrew J. Mannes, Jeih-San Liow, Vanessa N. Barth, Cheryl L. Morse, Sami S. Zoghbi, Nicolas Dreyfus, Robert L. Gladding, Cynthia Darshini Jesudason, Robert B. Innis, Sergey Shcherbinin
Rok vydání: 2020
Předmět:
Zdroj: Science Translational Medicine. 12
ISSN: 1946-6242
1946-6234
DOI: 10.1126/scitranslmed.aau2939
Popis: We aimed to develop effective radioligands for quantifying brain O-linked-β-N-acetyl-glucosamine (O-GlcNAc) hydrolase (OGA) using positron emission tomography in living subjects as tools for evaluating drug target engagement. Posttranslational modifications of tau, a biomarker of Alzheimer's disease, by O-GlcNAc through the enzyme pair OGA and O-GlcNAc transferase (OGT) are inversely related to the amounts of its insoluble hyperphosphorylated form. Increase in tau O-GlcNAcylation by OGA inhibition is believed to reduce tau aggregation. LSN3316612, a highly selective and potent OGA ligand [half-maximal inhibitory concentration (IC50) = 1.9 nM], emerged as a lead ligand after in silico analysis and in vitro evaluations. [3H]LSN3316612 imaged and quantified OGA in postmortem brains of rat, monkey, and human. The presence of fluorine and carbonyl functionality in LSN3316612 enabled labeling with positron-emitting fluorine-18 or carbon-11. Both [18F]LSN3316612 and [11C]LSN3316612 bound reversibly to OGA in vivo, and such binding was blocked by pharmacological doses of thiamet G, an OGA inhibitor of different chemotype, in monkeys. [18F]LSN3316612 entered healthy human brain avidly (~4 SUV) without radiodefluorination or adverse effect from other radiometabolites, as evidenced by stable brain total volume of distribution (VT) values by 110 min of scanning. Overall, [18F]LSN3316612 is preferred over [11C]LSN3316612 for future human studies, whereas either may be an effective positron emission tomography radioligand for quantifying brain OGA in rodent and monkey.
Databáze: OpenAIRE
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