Kehr J, Ungerstedt U
Department of Pharmacology, Karolinska Institute, Stockholm, Sweden.
J Neurochem. 1988 Oct;51(4):1308-10. doi: 10.1111/j.1471-4159.1988.tb03101.x.
A method for rapid, automated (less than 5 min), and sensitive (detection limit 50 fmol/10 microliter) determination of gamma-aminobutyric acid (GABA) is described. The method is based on precolumn derivatization with o-phthaldialdehyde/t-butylthiol reagent and separation by reverse-phase HPLC with electrochemical detection under isocratic conditions. A 100 X 4 mm Nucleosil 3 C18 column was used; the mobile phase consisted of 0.15 M sodium acetate, 1 mM EDTA (pH 5.4), and 50% acetonitrile; the flow rate was 0.8 ml/min. The potential of the glassy carbon working electrode was +0.75 V. The method allows for the monitoring of GABA levels in the extracellular fluid sampled by microdialysis as documented in the present study when 0.5 mM nipecotic acid is infused via the probe, or 3-mercaptopropionic acid is injected at a dose of 100 mg/kg i.p. There was a 15-fold increase of extracellular GABA after nipecotic acid, whereas in the second case the inhibition of GABA synthesis was followed by a 74% decrease of GABA as compared to basal levels.
本文描述了一种快速、自动化(不到5分钟)且灵敏(检测限为50飞摩尔/10微升)测定γ-氨基丁酸(GABA)的方法。该方法基于邻苯二甲醛/叔丁硫醇试剂进行柱前衍生化,并在等度条件下通过反相高效液相色谱结合电化学检测进行分离。使用了一根100×4毫米的Nucleosil 3 C18柱;流动相由0.15 M醋酸钠、1 mM乙二胺四乙酸(pH 5.4)和50%乙腈组成;流速为0.8毫升/分钟。玻碳工作电极的电位为+0.75伏。如本研究所示,当通过探针注入0.5 mM的哌啶酸,或腹腔注射剂量为100毫克/千克的3-巯基丙酸时,该方法可用于监测通过微透析采集的细胞外液中的GABA水平。注入哌啶酸后细胞外GABA增加了15倍,而在第二种情况下,与基础水平相比,GABA合成受到抑制后GABA减少了74%。