| Literature DB >> 27650910 |
Junchao Tong1, Romina Mizrahi1, Sylvain Houle1, Stephen J Kish1, Isabelle Boileau1, Jose Nobrega1, Pablo M Rusjan1, Alan A Wilson1.
Abstract
In a recent clinical trial, the drug BIA 10-2474, a putative fatty acid amide hydrolase(FAAH) inhibitor, was responsible for severe adverse events (SAEs), including one death. To date, there has been little reliable information divulged about the potency of BIA 10-2474 at FAAH in the central nervous system. We synthesised BIA 10-2474 and determined its ability to inhibit FAAH ex vivo in rat brain using a FAAH selective radiotracer. BIA 10-2474 proved to be a potent FAAH inhibitor with IC50s of 50-70 µg/kg (i.p.) in various brain regions. This information may be useful for determining the cause of the SAEs.Entities:
Keywords: Animal models; brain imaging; clinical trials; positron emission tomography; receptor imaging
Mesh:
Substances:
Year: 2016 PMID: 27650910 PMCID: PMC5669339 DOI: 10.1177/0271678X16668890
Source DB: PubMed Journal: J Cereb Blood Flow Metab ISSN: 0271-678X Impact factor: 6.200