Bliss T V, Douglas R M, Errington M L, Lynch M A
J Physiol. 1986 Aug;377:391-408. doi: 10.1113/jphysiol.1986.sp016193.
The relationship between long-term potentiation (l.t.p.) and the release of endogenous amino acid transmitters has been investigated in the dentate gyrus of rats anaesthetized with urethane. The molecular layer was perfused with artificial cerebrospinal fluid using a push-pull cannula. The perfusate was collected and analysed for glutamate, aspartate, glycine, glutamine and gamma-aminobutyric acid (GABA) using high-performance liquid chromatography (h.p.l.c.) with fluorometric detection. Recording electrodes were attached to the cannula to enable responses evoked by test stimuli to the perforant path to be monitored in the molecular and cell body layers. Perfusion was continued for 3 h while test stimuli were delivered to the perforant path at 30 s intervals. In the control group (n = 8), no further stimulation was given. In a second group (n = 8), a single high-frequency train (250 Hz for 200 ms) was delivered at the end of the first hour to induce l.t.p. The average potentiation of the slope of the excitatory post-synaptic potential (e.p.s.p.) 2 h later was 15%. In a third group (n = 8), the train to the perforant path was paired with a train to the commissural input to the dentate gyrus, a procedure which blocks the induction of l.t.p. In the potentiated group, there was an increase in the concentrations of glutamate and aspartate following the induction of l.t.p., relative to the decline seen in corresponding periods of the control group. This increase remained statistically significant for 1.5 h in the case of glutamate and for 45 min in the case of aspartate. There were no l.t.p.-associated changes in the release of glutamine or glycine; there was an indication that l.t.p. may be associated with a decrease in the release of GABA. Increasing the frequency and intensity of perforant path activation resulted in enhanced concentrations of glutamate and aspartate in the perfusate; no such changes occurred when granule cells were activated antidromically. We discuss the origin of the relative increases in the concentration of glutamate and aspartate which are found in the perfusate following the induction of l.t.p. and conclude that the most likely source is a sustained increase in activity-dependent release of these amino acids from perforant path terminals.(ABSTRACT TRUNCATED AT 400 WORDS)
在使用氨基甲酸乙酯麻醉的大鼠齿状回中,研究了长时程增强(LTP)与内源性氨基酸递质释放之间的关系。使用推挽式套管向分子层灌注人工脑脊液。收集灌注液,并用带荧光检测的高效液相色谱(HPLC)分析谷氨酸、天冬氨酸、甘氨酸、谷氨酰胺和γ-氨基丁酸(GABA)。将记录电极连接到套管上,以便在分子层和细胞体层监测由测试刺激穿通路径诱发的反应。在以30秒的间隔向穿通路径施加测试刺激的同时,持续灌注3小时。在对照组(n = 8)中,不再给予进一步刺激。在第二组(n = 8)中,在第一小时结束时给予单次高频串刺激(250 Hz,持续200毫秒)以诱导LTP。2小时后兴奋性突触后电位(EPSP)斜率的平均增强为15%。在第三组(n = 8)中,向穿通路径的串刺激与向齿状回联合输入的串刺激配对,该操作可阻断LTP的诱导。在增强组中,相对于对照组相应时间段内的下降,诱导LTP后谷氨酸和天冬氨酸的浓度增加。谷氨酸的这种增加在1.5小时内保持统计学显著,天冬氨酸的这种增加在45分钟内保持统计学显著。谷氨酰胺或甘氨酸的释放没有与LTP相关的变化;有迹象表明LTP可能与GABA释放的减少有关。增加穿通路径激活的频率和强度导致灌注液中谷氨酸和天冬氨酸的浓度升高;当颗粒细胞被逆向激活时,没有发生这种变化。我们讨论了诱导LTP后灌注液中谷氨酸和天冬氨酸浓度相对增加的来源,并得出结论,最可能的来源是这些氨基酸从穿通路径终末的活动依赖性释放持续增加。(摘要截断于400字)