Zhang W Q, Rogers B C, Tandon P, Hudson P M, Sobotka T J, Hong J S, Tilson H A
Laboratory of Molecular and Integrative Neuroscience, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
Neurotoxicology. 1990 Winter;11(4):593-600.
The ventral hippocampi of male, Fischer-344 rats were implanted with microdialysis probes and the effects of systemically administered kainic acid (KA) (8 mg/kg, s.c.) on the in vivo release of amino acids were measured for four hours after administration. In order to measure GABA release in vivo, gamma-vinyl-GABA (GVG), an irreversible inhibitor of GABA transaminase, was injected intrahippocampally prior to perfusion. GVG pretreatment resulted in measurable levels of GABA in the perfusate without significant effects on the release of aspartate, glutamate, glutamine, glycine or taurine. Following GVG pretreatment systemic administration of KA produced a time-dependent increase in GABA, as well as all other amino acids except glutamine, which was initially decreased. These results show for the first time that systemically administered KA increases extracellular GABA levels, an effect previously reported only in vitro. These data suggest that prior to destruction of GABA-containing interneurons in the hippocampus, there is an increased activity of those GABA interneurons reflected as an increase in extracellular GABA levels.
在雄性Fischer-344大鼠的腹侧海马体植入微透析探针,在腹腔注射8mg/kg的红藻氨酸(KA)后4小时,测量系统给药对体内氨基酸释放的影响。为了测量体内γ-氨基丁酸(GABA)的释放,在灌注前向海马体内注射GABA转氨酶的不可逆抑制剂γ-乙烯基-GABA(GVG)。GVG预处理使灌注液中GABA达到可测量水平,且对天冬氨酸、谷氨酸、谷氨酰胺、甘氨酸或牛磺酸的释放无显著影响。在GVG预处理后,系统给药KA使GABA以及除谷氨酰胺(最初降低)外的所有其他氨基酸呈时间依赖性增加。这些结果首次表明,系统给药KA可增加细胞外GABA水平,这一效应此前仅在体外有报道。这些数据表明,在海马体中含GABA的中间神经元被破坏之前,这些GABA中间神经元的活性增加,表现为细胞外GABA水平升高。