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Development of a tonic form of synaptic inhibition in rat cerebellar granule cells resulting from persistent activation of GABAA receptors.

机译:GABAA受体的持续激活导致大鼠小脑颗粒细胞中突触抑制的强直形式的发展。

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摘要

1. To investigate the origin and functional significance of a recently described tonic GABAA receptor-mediated conductance in cerebellar granule cells we have made recordings from cells in cerebellar slices from rats of different ages (postnatal days P4 to P28). 2. During development there was a dramatic change in the properties of GABA-mediated synaptic transmission. The contribution to GABAA receptor-mediated charge transfer from the tonic conductance (GGABA), relative to that resulting from discrete spontaneous postsynaptic currents (sPSCs), was increased from 5% at P7 to 99% at P21. GGABA was reduced by bicuculline, tetrodotoxin and by lowering extracellular Ca2+, and was initially present only in those cells which exhibited sPSCs. 3. At P7 sPSCs were depolarizing, occasionally triggering a single action potential. By P18 the GABA reversal potential was shifted close to the resting potential and GGABA produced a shunting inhibition. Removal of GGABA by bicuculline increased granule cell excitability in response to current injection. 4. This novel tonic inhibition is present despite the low number of Golgi cell synapses on individual granule cells and appears to result from 'overspill' of synaptically released GABA leading to activation of synaptic and extrasynaptic GABAA receptors.
机译:1.为了研究最近描述的强直GABAA受体介导的小脑颗粒细胞电导的起源和功能意义,我们从不同年龄(出生后P4至P28)的小脑切片中的细胞中进行了录音。 2.在发育过程中,GABA介导的突触传递特性发生了巨大变化。相对于离散的自发突触后电流(sPSCs)所产生的影响,相对于自发性突触后突触电流(sPSCs)的影响,补语电导(GGABA)对GABAA受体介导的电荷转移的贡献从P7的5%增加到P21的99%。 GGABA被双小分子,河豚毒素和降低的细胞外Ca2 +所减少,最初仅存在于那些表现出sPSC的细胞中。 3.在P7时,sPSC处于去极化状态,偶尔触发单个动作电位。通过P18,GABA逆转电位接近静息电位,而GGABA产生分流抑制作用。通过双小分子去除GGABA可增加对当前注射剂的颗粒细胞兴奋性。 4.尽管单个颗粒细胞上高尔基体细胞突触的数量很少,但仍存在这种新的强直抑制作用,并且似乎是由于突触释放的GABA的“溢出”导致突触和突触外GABAA受体的活化而引起的。

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