TY - JOUR
T1 - Utilizing PET and MALDI Imaging for Discovery of a Targeted Probe for Brain Endocannabinoid α/β-Hydrolase Domain 6 (ABHD6)
AU - Mardon, Karine
AU - Patel, Jayendra Z.
AU - Savinainen, Juha R.
AU - Stimson, Damion H.R.
AU - Oyagawa, Caitlin R.M.
AU - Grimsey, Natasha L.
AU - Migotto, Mary Anne
AU - Njiru, Grace F.M.
AU - Hamilton, Brett R.
AU - Cowin, Gary
AU - Yli-Kauhaluoma, Jari
AU - Vanduffel, Wim
AU - Blakey, Idriss
AU - Bhalla, Rajiv
AU - Cawthorne, Christopher
AU - Celen, Sofie
AU - Bormans, Guy
AU - Thurecht, Kristofer J.
AU - Ahamed, Muneer
N1 - Publisher Copyright:
© 2023 American Chemical Society. All rights reserved.
PY - 2023/1/12
Y1 - 2023/1/12
N2 - Multimodal imaging provides rich biological information, which can be exploited to study drug activity, disease associated phenotypes, and pharmacological responses. Here we show discovery and validation of a new probe targeting the endocannabinoid α/β-hydrolase domain 6 (ABHD6) enzyme by utilizing positron emission tomography (PET) and matrix-assisted laser desorption/ionization (MALDI) imaging. [18F]JZP-MA-11 as the first PET ligand for in vivo imaging of the ABHD6 is reported and specific uptake in ABHD6-rich peripheral tissues and major brain regions was demonstrated using PET. A proof-of-concept study in nonhuman primate confirmed brain uptake. In vivo pharmacological response upon ABHD6 inhibition was observed by MALDI imaging. These synergistic imaging efforts used to identify biological information cannot be obtained by a single imaging modality and hold promise for improving the understanding of ABHD6-mediated endocannabinoid metabolism in peripheral and central nervous system disorders.
AB - Multimodal imaging provides rich biological information, which can be exploited to study drug activity, disease associated phenotypes, and pharmacological responses. Here we show discovery and validation of a new probe targeting the endocannabinoid α/β-hydrolase domain 6 (ABHD6) enzyme by utilizing positron emission tomography (PET) and matrix-assisted laser desorption/ionization (MALDI) imaging. [18F]JZP-MA-11 as the first PET ligand for in vivo imaging of the ABHD6 is reported and specific uptake in ABHD6-rich peripheral tissues and major brain regions was demonstrated using PET. A proof-of-concept study in nonhuman primate confirmed brain uptake. In vivo pharmacological response upon ABHD6 inhibition was observed by MALDI imaging. These synergistic imaging efforts used to identify biological information cannot be obtained by a single imaging modality and hold promise for improving the understanding of ABHD6-mediated endocannabinoid metabolism in peripheral and central nervous system disorders.
UR - https://www.scopus.com/pages/publications/85144301732
U2 - 10.1021/acs.jmedchem.2c01485
DO - 10.1021/acs.jmedchem.2c01485
M3 - Article
C2 - 36516997
AN - SCOPUS:85144301732
SN - 0022-2623
VL - 66
SP - 538
EP - 552
JO - Journal of medicinal chemistry
JF - Journal of medicinal chemistry
IS - 1
ER -