Chang H H, Michaelis E K, Roy S
Neurochem Res. 1984 Jul;9(7):903-15. doi: 10.1007/BF00964522.
L-Glutamic acid (L-Glu) and other excitatory amino acids and amino acid analogs enhanced [35S]thiocyanate (SCN-) uptake in isolated-resealed synaptic membrane vesicles. The SCN- uptake was used as a measure of membrane depolarization to evaluate the characteristics of functional excitatory amino acid receptors in the synaptic membranes. N-Methyl-D-aspartate (NMDA) and L-Glu produced additive effects on SCN- accumulation indicating the presence of distinct L-Glu and NMDA receptors. On the other hand, kainic acid (KA) and L-Glu shared either common receptor sites or ion channels. The effects of antagonists on NMDA, L-Glu, and KA stimulation of SCN- influx were consistent with previously reported electrophysiologic observations in intact neurons.
L-谷氨酸(L-Glu)以及其他兴奋性氨基酸和氨基酸类似物可增强分离再封闭的突触膜囊泡对[35S]硫氰酸盐(SCN-)的摄取。SCN-摄取被用作膜去极化的指标,以评估突触膜中功能性兴奋性氨基酸受体的特性。N-甲基-D-天冬氨酸(NMDA)和L-Glu对SCN-积累产生相加效应,表明存在不同的L-Glu和NMDA受体。另一方面,海人酸(KA)和L-Glu共享共同的受体位点或离子通道。拮抗剂对NMDA、L-Glu和KA刺激SCN-内流的影响与先前在完整神经元中报道的电生理观察结果一致。