Kabuto H, Yokoi I, Mizukawa K, Mori A
Department of Neurochemistry, Okayama University Medical School, Japan.
Neurochem Res. 1989 Nov;14(11):1075-80. doi: 10.1007/BF00965613.
3-((+-)-2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) is an antagonist at the N-methyl-D-aspartate (NMDA) subtype of glutamate receptor. In the present study, levels of dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA) and 5-hydroxyindolacetic acid (5-HIAA) were measured after intracerebroventricular injection of NMDA, CPP or both in rat striatum using a brain dialysis method. The injection of NMDA produced a significant increase in DOPAC level. HVA level was also increased by NMDA injection. The level of 5-HIAA was not affected by NMDA injection. The injection of CPP had no effect on DOPAC, HVA and 5-HIAA levels. The injection of CPP restrained the increase of DOPAC and HVA levels induced by NMDA injection. The results suggest that intracerebral injection of NMDA may increase dopamine release from rat striatum, but have no effect on serotonin release. Furthermore, CPP inhibits NMDA induced release of dopamine.
3-((±)-2-羧基哌嗪-4-基)丙基-1-膦酸(CPP)是谷氨酸受体N-甲基-D-天冬氨酸(NMDA)亚型的拮抗剂。在本研究中,采用脑透析法在大鼠纹状体内脑室内注射NMDA、CPP或两者后,测定二羟基苯乙酸(DOPAC)、高香草酸(HVA)和5-羟吲哚乙酸(5-HIAA)的水平。注射NMDA后,DOPAC水平显著升高。注射NMDA也使HVA水平升高。5-HIAA水平不受NMDA注射的影响。注射CPP对DOPAC、HVA和5-HIAA水平无影响。注射CPP可抑制NMDA注射诱导的DOPAC和HVA水平升高。结果表明,脑室内注射NMDA可能增加大鼠纹状体中多巴胺的释放,但对5-羟色胺的释放无影响。此外,CPP可抑制NMDA诱导的多巴胺释放。