Zhang Nanjing, Tomizawa Motohiro, Casida John E
Environmental Chemistry and Toxicology Laboratory, Department of Environmental Science, Policy and Management, University of California, 114 Wellman Hall, Berkeley, CA 94720-3112, USA.
Neurosci Lett. 2004 Nov 16;371(1):56-9. doi: 10.1016/j.neulet.2004.08.040.
The principal mammalian brain nicotinic acetylcholine receptors (nAChRs) are the alpha-bungarotoxin (alpha-BGT)-insensitive alpha 4 beta 2 and the alpha-BGT-sensitive alpha 7 subtypes assayed with radiolabeled nicotinoids and alpha-BGT, respectively. Drosophila head membranes bind the insecticide radioligand [(3)H]imidacloprid ([(3)H]IMI) and [(3)H]alpha-BGT with K(D) 5.7 and 2.7 nM and B(max) 980 and 1400 fmol/mg protein, respectively. The hypothesis that [(3)H]IMI at 2.5 or 20 nM and [(3)H]alpha-BGT at 1 or 10 nM bind to distinct sites or subtypes is tested by using these radioligands alone and together in simultaneous dual binding experiments. These studies show no interference by one radioligand in the binding of the other one, i.e., independent binding, and that both unlabeled IMI and alpha-BGT give biphasic displacement curves. The pharmacological profiles of [(3)H]IMI and [(3)H]alpha-BGT suggest distinct binding sites for the two radioligands. These findings are consistent with those obtained with hybrid receptors assembled from Drosophila alpha subunits and a vertebrate beta subunit and with immunological and protein biochemical approaches. This study, therefore, provides direct evidence for distinct IMI- and alpha-BGT-sensitive sites or subtypes in Drosophila brain.
主要的哺乳动物脑烟碱型乙酰胆碱受体(nAChRs)是α-银环蛇毒素(α-BGT)不敏感的α4β2亚型和α-BGT敏感的α7亚型,分别用放射性标记的烟碱类药物和α-BGT进行测定。果蝇头部膜分别以5.7 nM和2.7 nM的解离常数(K(D))以及980和1400 fmol/mg蛋白质的最大结合量(B(max))与杀虫剂放射性配体[³H]吡虫啉([³H]IMI)和[³H]α-BGT结合。通过在同步双重结合实验中单独和共同使用这些放射性配体,来检验2.5 nM或20 nM的[³H]IMI以及1 nM或10 nM的[³H]α-BGT是否与不同位点或亚型结合的假设。这些研究表明一种放射性配体不会干扰另一种的结合,即独立结合,并且未标记的IMI和α-BGT都给出双相位移曲线。[³H]IMI和[³H]α-BGT的药理学特征表明这两种放射性配体具有不同的结合位点。这些发现与用果蝇α亚基和脊椎动物β亚基组装的杂交受体以及免疫和蛋白质生化方法所获得的结果一致。因此,本研究为果蝇脑中不同的IMI敏感位点和α-BGT敏感位点或亚型提供了直接证据。