Poisnel Géraldine, Quentin Thomas, Barré Louisa, Coquerel Antoine, Debruyne Danièle
UMR CEA-2-FRE-CNRS 2698 Research group, Center Cyceron, Caen, France.
J Neurosci Methods. 2006 Jun 30;154(1-2):60-7. doi: 10.1016/j.jneumeth.2005.11.012. Epub 2006 Jan 19.
A new approach of competitive displacement binding assay using brain sections and a beta-imager is presented to estimate binding parameters such as affinity and selectivity of new compounds or to characterize receptor families or subtypes of receptors in small brain regions. This method includes a preliminary saturation assay intended to define the optimal concentration of displaceable radio-labeled ligand followed by the determination of displacement constants (IC(50) and K(i)) in cerebral regions rich in studied receptor. The technique application was demonstrated in seven rat brain structures, using displacement of the selective tritiated mu-opioid ligand [(3)H]-DAMGO by six opioid ligands: a specific agonist (DAMGO), less specific agonists (morphine, remifentanil), a non-specific antagonist with good affinity for mu receptors (naloxone) and ligands specific of other opioid subtypes (naltrindole, U50.488). Radioactivity counts were collected during 48 h. The assay-validation was performed by measuring intra- and inter-assay variation on determinations and by comparing presently obtained K(i) values with data from recognised methodologies. Both prove the accuracy of the proposed method.
本文介绍了一种使用脑切片和β成像仪的竞争性置换结合测定新方法,用于估计新化合物的结合参数,如亲和力和选择性,或表征小脑区域中受体家族或受体亚型。该方法包括一个初步的饱和测定,旨在确定可置换放射性标记配体的最佳浓度,随后在富含研究受体的脑区测定置换常数(IC(50)和K(i))。使用六种阿片类配体置换选择性氚化μ阿片配体[(3)H]-DAMGO,在七种大鼠脑结构中展示了该技术的应用:一种特异性激动剂(DAMGO)、特异性较低的激动剂(吗啡、瑞芬太尼)、对μ受体具有良好亲和力的非特异性拮抗剂(纳洛酮)以及其他阿片亚型特异性配体(纳曲吲哚、U50.488)。在48小时内收集放射性计数。通过测量测定中的批内和批间变异,并将当前获得的K(i)值与公认方法的数据进行比较,进行了测定验证。两者均证明了所提出方法的准确性。