Bertoglio, Daniele

Cybulska, Klaudia

Dominguez, Celia

Kertesz, Istvan

Korat, Spela

Liu, Longbin

Miranda Menchaca, Alan

Mrzljak, Ladislav

Munoz-Sanjuan, Ignacio

Skinbjerg, Mette

Staelens, Steven

Stroobants, Sigrid

Verhaeghe, Jeroen

Wyffels, Leonie

Abstract: Synaptic pathology is associated with several brain disorders, thus positron emission tomography (PET) imaging of synaptic vesicle glycoprotein 2A (SV2A) using the radioligand [C-11]UCB-J may provide a tool to measure synaptic alterations. Given the pivotal role of mouse models in understanding neuropsychiatric and neurodegenerative disorders, this study aims to validate and characterize [C-11]UCB-J in mice. We performed a blocking study to verify the specificity of the radiotracer to SV2A, examined kinetic models using an image-derived input function (IDIF) for quantification of the radiotracer, and investigated the in vivo metabolism. Regional TACs during baseline showed rapid uptake of [C-11]UCB-J into the brain. Pretreatment with levetiracetam confirmed target engagement in a dose-dependent manner. V-T (IDIF) values estimated with one- and two-tissue compartmental models (1TCM and 2TCM) were highly comparable (r=0.999, p < 0.0001), with 1TCM performing better than 2TCM for K-1 (IDIF). A scan duration of 60 min was sufficient for reliable V-T (IDIF) and K-1 (IDIF) estimations. In vivo metabolism of [C-11]UCB-J was relatively rapid, with a parent fraction of 22.5 +/- 4.2% at 15 min p.i. In conclusion, our findings show that [C-11]UCB-J selectively binds to SV2A with optimal kinetics in the mouse representing a promising tool to noninvasively quantify synaptic density in comparative or therapeutic studies in neuropsychiatric and neurodegenerative disorder models

Institutional Repository Universiteit Antwerpen

Validation and noninvasive kinetic modeling of <tex>[^{11}C]$</tex>UCB-J PET imaging in mice

Validation and noninvasive kinetic modeling of <tex>[^{11}C]$</tex>UCB-J PET imaging in mice

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Institutional Repository Universiteit Antwerpen