Segovia G, Porras A, Mora F
Department of Physiology, Faculty of Medicine, University Complutense, Madrid, Spain.
Neurochem Res. 1997 Dec;22(12):1491-7. doi: 10.1023/a:1021958613125.
4-aminopyridine (4-AP) is a voltage-sensitive K(+)-channel blocker extensively used in in vitro experiments as a depolarizing agent for the release of glutamate (GLU). This research investigated whether 4-AP could be used in in vivo experiments using microdialysis. For that, the effects of 4-AP on the extracellular concentrations of glutamate (GLU), glutamine (GLN), taurine (TAU) and citrulline (CIT) in striatum of the freely moving rat were investigated. The effects of 4-AP were compared with those produced by perfusion with a high K+ (100 mM) medium. Intrastriatal perfusion with 4-AP (1, 5 and 10 mM) produced no effects on extracellular [GLU], [TAU] and [CIT], but decreased extracellular [GLN]. Perfusion with a high K+ (100 mM) medium increased extracellular [GLU] and [TAU], decreased extracellular [GLN], and had no effects on [CIT]. To test whether the lack of effects of 4-AP on extracellular [GLU] was due to GLU uptake mechanisms, 4-AP was perfused after a previous inhibition of GLU uptake with L-trans-pyrrolidine-2,4-dicarboxylic acid (PDC). Under the effects of PDC (1 mM), 4-AP (1 mM) had no effects on extracellular [GLU], [TAU] and [CIT], but decreased extracellular [GLN]. These results show that 4-AP decreased extracellular [GLN] but failed to produce a significant release of GLU in striatum of the freely moving rat. Thus, 4-AP can not be used as a depolarizing agent for stimulating the release of GLU in in vivo studies using microdialysis.
4-氨基吡啶(4-AP)是一种电压敏感性钾离子通道阻滞剂,在体外实验中广泛用作谷氨酸(GLU)释放的去极化剂。本研究调查了4-AP是否可用于体内微透析实验。为此,研究了4-AP对自由活动大鼠纹状体中谷氨酸(GLU)、谷氨酰胺(GLN)、牛磺酸(TAU)和瓜氨酸(CIT)细胞外浓度的影响。将4-AP的作用与用高钾(100 mM)培养基灌注所产生的作用进行了比较。纹状体内灌注4-AP(1、5和10 mM)对细胞外[GLU]、[TAU]和[CIT]无影响,但降低了细胞外[GLN]。用高钾(100 mM)培养基灌注增加了细胞外[GLU]和[TAU],降低了细胞外[GLN],对[CIT]无影响。为了测试4-AP对细胞外[GLU]缺乏作用是否归因于GLU摄取机制,在用L-反式-吡咯烷-2,4-二羧酸(PDC)预先抑制GLU摄取后灌注4-AP。在PDC(1 mM)的作用下,4-AP(1 mM)对细胞外[GLU]、[TAU]和[CIT]无影响,但降低了细胞外[GLN]。这些结果表明,4-AP降低了细胞外[GLN],但未能在自由活动大鼠的纹状体中显著释放GLU。因此,在使用微透析的体内研究中,4-AP不能用作刺激GLU释放的去极化剂。