Paternain A V, Morales M, Lerma J
Departamento de Plasticidad Neural, Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Neuron. 1995 Jan;14(1):185-9. doi: 10.1016/0896-6273(95)90253-8.
Although both protein and mRNAs for kainate receptor subunits are abundant in several brain regions, the responsiveness of AMPA receptors to kainate has made it difficult to demonstrate the presence of functional kainate-type receptors in native cells. Recently, however, we have shown that many hippocampal neurons in culture express glutamate receptors of the kainate type. The large nondesensitizing response that kainate induces at AMPA receptors precludes detection and analysis of smaller, rapidly desensitizing currents induced by kainate at kainate receptors. Consequently, the functional significance of these strongly desensitizing glutamate receptors remains enigmatic. We report here that the family of new noncompetitive antagonists of AMPA receptors (GYKI 52466 and 53655) minimally affects kainate-induced responses at kainate receptors while completely blocking AMPA receptor-mediated currents, making it possible to separate the responses mediated by each receptor. These compounds will allow determination of the role played by kainate receptors in synaptic transmission and plasticity in the mammalian brain, as well as evaluation of their involvement in neurotoxicity.
尽管在几个脑区中,红藻氨酸受体亚基的蛋白质和信使核糖核酸都很丰富,但AMPA受体对红藻氨酸的反应性使得在天然细胞中证明功能性红藻氨酸型受体的存在变得困难。然而,最近我们发现,许多培养的海马神经元表达红藻氨酸型谷氨酸受体。红藻氨酸在AMPA受体上诱导的大的非脱敏反应排除了对红藻氨酸在红藻氨酸受体上诱导的较小的、快速脱敏电流的检测和分析。因此,这些强烈脱敏的谷氨酸受体的功能意义仍然是个谜。我们在此报告,AMPA受体的新型非竞争性拮抗剂家族(GYKI 52466和53655)对红藻氨酸在红藻氨酸受体上诱导的反应影响极小,同时完全阻断AMPA受体介导的电流,从而有可能区分每种受体介导的反应。这些化合物将有助于确定红藻氨酸受体在哺乳动物大脑突触传递和可塑性中所起的作用,以及评估它们在神经毒性中的作用。