Kraus J E, McNamara J O
Department of Neurobiology, Duke University Medical Center, 401 Bryan Research Building, Durham, NC, 27710, USA.
Brain Res Mol Brain Res. 1998 Oct 30;61(1-2):114-20. doi: 10.1016/s0169-328x(98)00220-4.
Kindling refers to a phenomenon in which repeated application of initially subconvulsive electrical stimulations produces limbic and clonic motor seizures of progressively increasing severity. Once established, the increased excitability is lifelong. A diversity of studies demonstrate that kindling results in long lasting (28 days) alterations of the functional and pharmacologic properties of NMDA receptors, indicating that kindling may cause changes intrinsic to the NMDA receptor itself. Our previous studies disclosed no differences in NMDA receptor subunit gene or splice isoform mRNA expression between control and kindled animals 28 days after the last kindled seizure. Here, we extend those earlier studies by measuring levels of subunit protein for NMDAR1, NR2A, and NR2B in the hippocampus of control and kindled animals, 28 days after the last kindled seizure. We report that kindling does not effect long-lasting changes in the levels of NMDA receptor subunit protein. Together these findings support the idea that alterations in NMDA receptor protein expression do not contribute to the novel properties of NMDA receptors induced by kindling.
点燃效应是指反复施加最初亚惊厥性电刺激会产生严重程度逐渐增加的边缘性和阵挛性运动性癫痫发作的一种现象。一旦确立,兴奋性增加会持续终生。大量研究表明,点燃效应会导致NMDA受体的功能和药理学特性发生长期(28天)改变,这表明点燃效应可能会引起NMDA受体本身内在的变化。我们之前的研究表明,在最后一次点燃性癫痫发作28天后,对照动物和点燃动物之间的NMDA受体亚基基因或剪接异构体mRNA表达没有差异。在此,我们通过测量最后一次点燃性癫痫发作28天后对照动物和点燃动物海马体中NMDAR1、NR2A和NR2B亚基蛋白的水平,扩展了早期的研究。我们报告称,点燃效应不会影响NMDA受体亚基蛋白水平的长期变化。这些发现共同支持了这样一种观点,即NMDA受体蛋白表达的改变不会导致点燃效应诱导的NMDA受体新特性。