Barrett-Jolley R
Department of Physiology, The Medical School, University of Birmingham, Edgbaston, Birmingham, B15 2TT.
Br J Pharmacol. 2001 Jul;133(5):673-8. doi: 10.1038/sj.bjp.0704128.
The GABA-related compound nipecotic acid is commonly used to inhibit GABA uptake. This report shows that nipecotic acid can also directly activate GABA(A)-like chloride channels. When applied to outside-out patches of paraventricular neurones, nipecotic acid (1 mM) activated inward unitary currents (approximately 3 pA at a holding potential of -60 mV, E(Cl)+44 mV). The EC(50) for ion channel activation was approximately 300 microM, 3 fold greater than that found for GABA itself in this preparation. The nipecotic acid activated channels had similar conductance and kinetic properties to those of GABA activated channels in the same patches, reversed near E(Cl) and were inhibited by bicuculline (3 microM). This study indicates that for experiments in which relatively high concentrations of nipecotic acid are used, possible direct GABA(A) receptor agonist properties should be considered.
与γ-氨基丁酸(GABA)相关的化合物哌啶酸常用于抑制GABA的摄取。本报告表明,哌啶酸还可直接激活GABA(A)样氯离子通道。当将其应用于室旁神经元的外向膜片时,哌啶酸(1 mM)可激活内向单位电流(在-60 mV的钳制电位下约为3 pA,氯离子平衡电位E(Cl)为+44 mV)。离子通道激活的半数有效浓度(EC(50))约为300 μM,是该制剂中GABA自身激活浓度的3倍。在同一膜片中,哌啶酸激活的通道与GABA激活的通道具有相似的电导和动力学特性,在E(Cl)附近反转,并被荷包牡丹碱(3 μM)抑制。本研究表明,在使用相对高浓度哌啶酸的实验中,应考虑其可能具有的直接GABA(A)受体激动剂特性。