Kouvelas E D, Greene L A
Brain Res. 1976 Aug 20;113(1):111-26. doi: 10.1016/0006-8993(76)90010-x.
The subcellular distribution, binding kinetics, pharmacologic properties and regional ontogeny of binding sites for alpha-[125I]bungarotoxins (alpha-[125I]BT) were studied in preparations of chick brain. Almost 95% of the specific binding was found in a 20,000 X g pellet. Two binding components were found, one with high (half-saturation at 1.5 X 10(-9) M) and another with low affinity for the toxin. The rate constants of association and dissociation of the toxin for the high-affinity site were found to be 3.5 X 10(4) M-1 - sec-1 and 3.8 X 10(-5) sec-1 (tau1/2 = 5.1 h, respectively). These data yielded a K alpha value of 1.1 X 10(-9) M. Nicotinic, but not muscarinic ligands were potent inhibitors of toxin binding at the high-affinity site. Thus, as in muscle, the binding site for toxin in chick brain appears to have the properties of a nicotinic acetylcholine (ACh) receptor. The ontogeny of the alpha-BT/ACh receptor was studied using homogenates of both whole brain and of discrete brain regions. In brain stem, optic lobe and cerebellum specific binding reached maximum levels in ovo and then decreased by maturity to values of 10,22 and 4.5 fmoles/mg protein, respectively. In contrast, whole brain and cerebral hemispheres reached plateau levels in ovo of 17 and 10 fmoles/mg protein, respectively. Major increases in total receptor number per region appeared in ovo between days 12 and 19 in brain stem and cerebellum, days 12 and 15 in optic lobes, and days 15 and 19 in hemispheres. The hemispheres were the only region to show a continued increase in total binding after hatching (3-fold increase by maturity). These findings are interpreted with respect to the development of chick brain and a model is suggested for the relationship between receptor ontogeny and neuronal differentiation and maturation.
在鸡脑制剂中研究了α-[¹²⁵I]银环蛇毒素(α-[¹²⁵I]BT)结合位点的亚细胞分布、结合动力学、药理特性及区域个体发生情况。几乎95%的特异性结合存在于20,000×g的沉淀中。发现有两种结合成分,一种对毒素具有高亲和力(在1.5×10⁻⁹M时达到半饱和),另一种对毒素的亲和力较低。毒素与高亲和力位点的结合和解离速率常数分别为3.5×10⁴M⁻¹·秒⁻¹和3.8×10⁻⁵秒⁻¹(半衰期分别为5.1小时)。这些数据得出的Kα值为1.1×10⁻⁹M。烟碱型而非毒蕈碱型配体是高亲和力位点上毒素结合的有效抑制剂。因此,与肌肉中一样,鸡脑中毒素的结合位点似乎具有烟碱型乙酰胆碱(ACh)受体的特性。利用全脑及离散脑区的匀浆研究了α-BT/ACh受体的个体发生情况。在脑干、视叶和小脑中,特异性结合在胚胎期达到最高水平,然后在成熟时分别降至10、22和4.5飞摩尔/毫克蛋白质的值。相比之下,全脑和大脑半球在胚胎期分别达到17和10飞摩尔/毫克蛋白质的平台水平。每个区域总受体数量的主要增加出现在胚胎期,脑干和小脑在第12至19天,视叶在第12至15天,半球在第15至19天。半球是唯一在孵化后总结合量持续增加的区域(成熟时增加3倍)。结合鸡脑的发育对这些发现进行了解释,并提出了一个受体个体发生与神经元分化和成熟之间关系的模型。