Behrends Jan C, Lambert John C, Jensen Kimmo
Department of Physiology, University of Munich, Pettenkoferstrasse 12, 80336 Munich, Germany.
Pflugers Arch. 2002 Mar;443(5-6):707-12. doi: 10.1007/s00424-001-0740-6. Epub 2001 Nov 1.
GABA(A) receptor-mediated Cl(-) currents were evoked by rapid and short (0.75-1.5 ms), focal iontophoretic applications of GABA to proximal dendrites of cultured striatal neurones. The mean amplitude (232 +/- 21.0 pA) was in the range of large miniature inhibitory postsynaptic currents (mIPSCs), while the 10-90% rise times (3.4 +/- 0.20 ms) and the time constants of decay (60.0 +/- 8.4 ms) were three times slower. Responses to paired-pulse application of GABA at inter-pulse intervals (IPIs) of 30, 100 and 300 ms showed no depression of the second response (R2) relative to the first (R1). At short IPIs, at which R1 and R2 showed temporal summation, the net amplitude of R2 (R2(net)) was partially occluded. Lowering the iontophoretic intensity during paired-pulse application at an IPI of 30 ms reduced R1 by 69.5 +/- 3.3%, while occlusion of R2(net) decreased significantly, indicating that the receptor occupancy had been lowered. During the course of ten pulses of GABA at 10 Hz, responses declined by 8.7 +/- 3.9%, which probably reflects slow cumulative desensitization. In conclusion, rapid focal iontophoresis of exogenous GABA onto GABA(A) receptors does not result in activity-dependent depression of the postsynaptic response. This result suggests that fast desensitization is unlikely to occur during repetitive GABA(A) receptor-mediated synaptic transmission in striatal neurones.
通过快速且短暂(0.75 - 1.5毫秒)地将GABA局部离子导入培养的纹状体神经元近端树突,诱发GABA(A)受体介导的Cl(-)电流。其平均幅度(232±21.0皮安)处于大型微小抑制性突触后电流(mIPSCs)范围内,而10 - 90%上升时间(3.4±0.20毫秒)和衰减时间常数(60.0±8.4毫秒)则慢三倍。在30、100和300毫秒的脉冲间隔(IPIs)下对GABA进行双脉冲施加时,相对于第一个反应(R1),第二个反应(R2)未出现抑制。在短IPIs时,R1和R2表现出时间总和,R2的净幅度(R2(net))部分被抵消。在30毫秒的IPIs下进行双脉冲施加时降低离子导入强度,R1降低了69.5±3.3%,而R2(net)的抵消则显著减少,表明受体占有率降低。在以10赫兹施加十个GABA脉冲的过程中,反应下降了8.7±3.9%,这可能反映了缓慢的累积脱敏。总之,将外源性GABA快速局部离子导入GABA(A)受体不会导致突触后反应的活动依赖性抑制。这一结果表明,在纹状体神经元中重复性GABA(A)受体介导的突触传递过程中不太可能发生快速脱敏。