Joëls M, Van Veldhuizen M, Urban I J, De Kloet E R
Brain Res. 1987 Feb 10;403(1):192-7. doi: 10.1016/0006-8993(87)90144-2.
In this study we examined the distribution of binding sites for [3H]N-acetyl-aspartylglutamate (NAAG) in the rat lateral septal nucleus (LSN) and the effect of iontophoretically applied NAAG on neuronal firing in this area. A high density of [3H]NAAG binding sites was found in the dorsolateral part of the LSN. Binding in the intermediate/ventral part of the LSN and medial septum was less dense. NAAG excited 75% of the dorsal neurons in the LSN, but only 36% of the cells in the intermediate/ventral part. Glutamic diethylester, an amino acid antagonist, depressed responses to NAAG to a similar extent as responses to quisqualate. The antagonist amino phosphonovaleric acid, which suppressed responses to N-methyl-D-aspartate almost completely, reduced NAAG-evoked responses only by 40%. A possible role of NAAG as excitatory transmitter in the LSN is discussed.
在本研究中,我们检测了[3H]N-乙酰天冬氨酰谷氨酸(NAAG)在大鼠外侧隔核(LSN)中的结合位点分布,以及离子导入NAAG对该区域神经元放电的影响。在LSN的背外侧部分发现了高密度的[3H]NAAG结合位点。LSN中间/腹侧部分和内侧隔区的结合密度较低。NAAG兴奋了LSN中75%的背侧神经元,但仅兴奋了中间/腹侧部分36%的细胞。氨基酸拮抗剂谷氨酸二乙酯对NAAG反应的抑制程度与对喹啉酸反应的抑制程度相似。拮抗剂氨基磷酸戊酸几乎完全抑制了对N-甲基-D-天冬氨酸的反应,仅使NAAG诱发的反应降低了40%。本文讨论了NAAG作为LSN中兴奋性递质的可能作用。