Rodríguez de Lores Arnaiz G, Schneider P, Peña C
Instituto de Biología Celular y Neurociencias Prof. Eduardo De Robertis, Facultad de Medicina, PROBICENE-CONICET, Universidad de Buenos Aires, Argentina.
Neurochem Res. 1999 Nov;24(11):1417-22. doi: 10.1023/a:1022536824190.
Two brain soluble fractions, named peaks I and II, which respectively stimulate and inhibit neuronal Na+, K+-ATPase activity, have been isolated by gel filtration in Sephadex G-50. Since cholinergic transmission seems related to such enzyme activity, in this study we evaluated the effect of brain peak I, peak II, a more purified fraction II-E and commercial ouabain, on specific binding of the muscarinic antagonist [3H]quinuclidinyl benzilate to membranes from rat cerebellum, hippocampus and cerebral cortex. We found that binding was increased by peak I and decreased by peak II, II-E and ouabain, all effects proving concentration-dependent. Since the changes exerted on the muscarinic receptor followed a pattern similar to the one already described for synaptosomal membrane Na+, K+-ATPase activity, both systems seem to interact at a functional level.
通过在葡聚糖凝胶G - 50上进行凝胶过滤,分离出了两种脑可溶性组分,分别命名为峰I和峰II,它们分别刺激和抑制神经元的钠钾ATP酶活性。由于胆碱能传递似乎与这种酶活性有关,在本研究中,我们评估了脑峰I、峰II、一种纯化程度更高的组分II - E和商用哇巴因对毒蕈碱拮抗剂[3H]喹核醇基苯甲酸酯与大鼠小脑、海马和大脑皮质膜特异性结合的影响。我们发现,峰I使结合增加,而峰II、II - E和哇巴因使结合减少,所有这些效应均呈浓度依赖性。由于对毒蕈碱受体产生的变化遵循与已描述的突触体膜钠钾ATP酶活性相似的模式,这两个系统似乎在功能水平上相互作用。