Conway P G, Brunswick D J
J Neurochem. 1985 Jul;45(1):206-9. doi: 10.1111/j.1471-4159.1985.tb05494.x.
The present study demonstrates that [3H]imipramine binds to both high- and low-affinity imipramine binding components on membranes prepared from rat cerebral cortex. Scatchard and computer analyses of saturation experiments using a wide range of [3H]imipramine concentrations (0.5 nM-50 nM) revealed the presence of two binding components. Inhibition experiments in which membranes were incubated with [3H]imipramine and various concentrations of unlabelled imipramine gave shallow inhibition curves with a Hill coefficient of 0.60 +/- 0.04. When dissociation rates of imipramine were studied, biphasic dissociation curves were obtained with apparent half-times of dissociation of 2.5 +/- 0.4 min and 18.5 +/- 2.5 min. Thus analysis of saturation, competition, and dissociation experiments indicate that [3H]imipramine binds to low as well as high-affinity binding sites in rat cortex.
本研究表明,[3H]丙咪嗪可与从大鼠大脑皮质制备的膜上的高亲和力和低亲和力丙咪嗪结合成分相结合。使用广泛的[3H]丙咪嗪浓度(0.5 nM - 50 nM)进行饱和实验的斯卡查德分析和计算机分析显示存在两种结合成分。在抑制实验中,将膜与[3H]丙咪嗪和各种浓度的未标记丙咪嗪一起孵育,得到的抑制曲线较浅,希尔系数为0.60±0.04。当研究丙咪嗪的解离速率时,获得了双相解离曲线,表观解离半衰期分别为2.5±0.4分钟和18.5±2.5分钟。因此,对饱和、竞争和解离实验的分析表明,[3H]丙咪嗪可与大鼠皮质中的低亲和力和高亲和力结合位点相结合。