| Literature DB >> 30789704 |
Vidya Narayanaswami1, Lindsey R Drake2,3, Allen F Brooks2, Jeffrey H Meyer1, Sylvain Houle1, Michael R Kilbourn2, Peter J H Scott2,3, Neil Vasdev1.
Abstract
In this Viewpoint, we highlight the history of positron emission tomography (PET) radiotracer development to quantify changes in monoamine oxidase (MAO)-A and -B enzyme expression or activity. MAO-A and MAO-B are critical for understanding monoaminergic pathways in psychiatric addiction disorders, and more recently in neurodegenerative disorders with MAO-B expression in astrogliosis. Unique radiochemical innovations have been shown for neuroimaging of MAOs including the clinical translation of irreversible propargylamine-based suicide inhibitors, application of deuterium-substitution to slow down metabolism, development of trapped metabolite imaging agents, and unique 11C-carbonylation chemistry toward novel high-affinity reversibly binding inhibitors.Entities:
Keywords: MAO-A; MAO-B; Monoamine oxidase; PET; carbon-11; fluorine-18
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Year: 2019 PMID: 30789704 DOI: 10.1021/acschemneuro.9b00081
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418