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

J. Tong, R. Mizrahi, S. Houle, S. Kish, I. Boileau, J. Nobrega, P. Rusjan, Alan A. Wilson
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引用次数: 10

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.
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BIA 10-2474对大鼠脑脂肪酸酰胺水解酶的抑制作用
在最近的一项临床试验中,药物BIA 10-2474,一种假定的脂肪酸酰胺水解酶(FAAH)抑制剂,导致严重不良事件(SAEs),包括一例死亡。迄今为止,关于BIA 10-2474在中枢神经系统FAAH中的效力,几乎没有可靠的信息泄露。我们合成了BIA 10-2474,并使用FAAH选择性放射性示踪剂测定了其在大鼠脑内体外抑制FAAH的能力。BIA 10-2474被证明是一种有效的FAAH抑制剂,在大脑各区域的ic50为50-70µg/kg (i.p.)。这些信息可能有助于确定sae的原因。
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