Department of Psychiatry, New York University School of Medicine, Room MHL HN-518, 550 First Ave., New York, NY 10016, USA.
J Neurosci Methods. 2012 Jan 15;203(1):19-27. doi: 10.1016/j.jneumeth.2011.08.044. Epub 2011 Sep 12.
The norepinephrine transporter (NET) is an important target for a wide variety of antidepressants and psychostimulants. Despite its prominence as a drug target, there is only one radioligand in use for NET competitive binding assays, [(3)H]nisoxetine. However, traditional [(3)H]nisoxetine binding protocols often give an underestimation for the affinity of certain classes of NET ligands, particularly cocaine and other tropanes. Here, we explore the feasibility of using the phenyltropane [(3)H]CFT for labeling human NET (hNET) in heterologous cell-based binding studies. Assays were optimized for time and protein content and specific, one-site binding was observed. Potencies of tested NET ligands for inhibition of [(3)H]CFT binding to whole cells (at physiological [Na(+)] and 25°C) were similar to potencies observed in the [(3)H]NE uptake assay. Inhibition constants (K(i)) for binding assays were highly correlated with uptake inhibition constants for all compounds tested (R(2)=0.99, p<0.0001). Cell-free membrane preparations did not display the same pharmacological profile. Under conditions routinely used for measuring [(3)H]nisoxetine binding to membrane preparations (4°C for 3h, [Na(+)] at 295 mM), the potency of nisoxetine and desipramine in inhibiting [(3)H]CFT binding became greater than that measured in a functional assay of [(3)H]NE uptake at physiological [Na(+)]. However, the opposite was true for CFT and cocaine. Interestingly, while investigating [(3)H]CFT as a potential NET radioligand, we uncovered evidence suggesting that CFT and nisoxetine are not mutually exclusive in binding to the NET. Dixon plots of the interaction between nisoxetine and CFT in inhibition of [(3)H]dopamine uptake by the NET indicate that the two compounds can simultaneously bind to the transporter.
去甲肾上腺素转运体(NET)是各种抗抑郁药和精神兴奋剂的重要靶标。尽管它作为药物靶标非常突出,但用于 NET 竞争性结合测定的放射性配体只有一种,即[(3)H]去甲丙咪嗪。然而,传统的[(3)H]去甲丙咪嗪结合方案通常会低估某些 NET 配体类别的亲和力,特别是可卡因和其他托烷类药物。在这里,我们探讨了使用苯并托烷[(3)H] CFT 标记人 NET(hNET)在异源细胞结合研究中的可行性。优化了时间和蛋白含量的测定,并观察到了特异性的单一位点结合。测试的 NET 配体对[(3)H] CFT 与整个细胞结合的抑制作用的效价(在生理[Na+]和 25°C)与在[(3)H]去甲肾上腺素摄取测定中观察到的效价相似。结合测定的抑制常数(K i)与所有测试化合物的摄取抑制常数高度相关(R 2=0.99,p<0.0001)。无细胞膜制剂未显示出相同的药理特征。在通常用于测量[(3)H]去甲丙咪嗪与膜制剂结合的条件下(4°C 3h,[Na+]为 295 mM),在生理[Na+]下,测定[(3)H] CFT 结合的去甲丙咪嗪和去甲替林的效价大于在生理[Na+]下测定的[(3)H]去甲肾上腺素摄取功能测定中的效价。然而,CFT 和可卡因的情况正好相反。有趣的是,在研究[(3)H] CFT 作为潜在的 NET 放射性配体时,我们发现了证据表明 CFT 和去甲丙咪嗪在结合 NET 时不是相互排斥的。Dixon 图显示,在 NET 抑制[(3)H]多巴胺摄取的过程中,去甲丙咪嗪和 CFT 之间的相互作用表明,这两种化合物可以同时结合到转运体上。