Verdoorn T A, Kleckner N W, Dingledine R
Department of Pharmacology and Neurobiology Curriculum, University of North Carolina, Chapel Hill 27514.
Science. 1987 Nov 20;238(4830):1114-6. doi: 10.1126/science.2825347.
N-methyl-D-aspartate (NMDA) activates a class of excitatory amino acid receptor involved in a variety of plastic and pathological processes in the brain. Quantitative study of the NMDA receptor has been difficult in mammalian neurons, because it usually exists with other excitatory amino acid receptors of overlapping pharmacological specificities. Xenopus oocytes injected with messenger RNA isolated from primary cultures of rat brain have now been used to study NMDA receptors. The distinguishing properties of neuronal NMDA receptors have been reproduced in this amphibian cell, including voltage-dependent block by magnesium, block by the NMDA receptor antagonist D-2-amino-5-phosphonovaleric acid, and potentiation by glycine. This preparation should facilitate the quantitative study of the regulation of NMDA receptor activation and serve as a tool for purification of the encoding messenger RNA.
N-甲基-D-天冬氨酸(NMDA)激活一类参与大脑多种可塑性和病理过程的兴奋性氨基酸受体。对NMDA受体进行定量研究在哺乳动物神经元中一直很困难,因为它通常与其他具有重叠药理学特异性的兴奋性氨基酸受体共存。现已利用注射了从大鼠脑原代培养物中分离出的信使核糖核酸的非洲爪蟾卵母细胞来研究NMDA受体。神经元NMDA受体的独特特性已在这种两栖类细胞中重现,包括镁离子对其电压依赖性阻断、NMDA受体拮抗剂D-2-氨基-5-磷酸缬氨酸对其的阻断以及甘氨酸对其的增强作用。这种制备方法应有助于对NMDA受体激活调节进行定量研究,并可作为纯化编码信使核糖核酸的一种工具。