Inhibition of fatty acid amide hydrolase by BIA 10-2474 in rat brain

被引:8
|
作者
Tong, Junchao [1 ]
Mizrahi, Romina [1 ]
Houle, Sylvain [1 ]
Kish, Stephen J. [1 ]
Boileau, Isabelle [1 ]
Nobrega, Jose [1 ]
Rusjan, Pablo M. [1 ]
Wilson, Alan A. [1 ]
机构
[1] Campbell Family Mental Hlth Res Inst, Ctr Addict & Mental Hlth, Res Imaging Ctr, 250 Coll St, Toronto, ON M5T 1R8, Canada
来源
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM | 2017年 / 37卷 / 11期
关键词
Animal models; brain imaging; clinical trials; positron emission tomography; receptor imaging; POSITRON-EMISSION-TOMOGRAPHY; PF-04457845; PET;
D O I
10.1177/0271678X16668890
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 IC(50)s of 50-70 mu g/kg (i.p.) in various brain regions. This information may be useful for determining the cause of the SAEs.
引用
收藏
页码:3635 / 3639
页数:5
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