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Temporal overlap of excitatory and inhibitory afferent input in guinea-pig CA1 pyramidal cells.

机译:豚鼠CA1锥体细胞中兴奋性和抑制性传入输入的时间重叠。

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1. The temporal interaction of evoked synaptic excitation and GABAA-mediated inhibition was examined in CA1 pyramidal cells. Single and paired intracellular recordings were carried out in pyramidal cell dendrites and somata, and interneurons of the guinea-pig hippocampal slice. Current-clamp, sharp electrode and whole-cell voltage-clamp recordings were made. 2. Kinetics of dendritic and somatic inhibitory responses were similar. Notably, kinetics of dendritic unitary IPSPs were as fast as kinetics of somatic unitary IPSPs. 3. GABAA-mediated influences were present throughout the orthodromic pyramidal cell EPSP/EPSC. Comparison of the kinetics of pharmacologically isolated monosynaptic IPSPs, IPSCs and inhibitory conductances (g GABAA), showed fastest kinetics for g GABAA. Close temporal overlap was observed between monosynaptic g GABAA and the rising phase of the evoked EPSP/EPSC. The onset of g GABAA coincided with or preceded onset of the EPSP/EPSC. 4. Onsets of feedforward IPSPs coincided with the rising phase of the pyramidal cell EPSP in > 80 % of paired recordings. Fastest feedforward inhibitory responses exerted near complete overlap with evoked excitation. 5. Onsets of recurrent IPSPs did not occur during the rising phase of the evoked EPSP, but > 3.0 ms after the peak of the pyramidal cell EPSP. 6. Orthodromically evoked interneuron spikes were observed at stimulation intensities that were below the threshold for eliciting EPSPs in concomitantly recorded pyramidal cells. The activation of feedforward inhibitory responses by weakest excitatory input, and the large temporal overlap between feedforward inhibition and evoked excitation, suggest that in situ any excitatory input in CA1 is effectively controlled by fast synaptic inhibition.
机译:1.在CA1锥体细胞中检测诱发的突触兴奋和GABAA介导的抑制的时间相互作用。在锥体细胞树突和躯体以及豚鼠海马切片的中间神经元中进行单和成对的细胞内记录。进行电流钳,尖电极和全细胞电压钳记录。 2.树突状和体细胞抑制反应的动力学相似。值得注意的是,树枝状单一IPSP的动力学与体细胞单一IPSP的动力学一样快。 3.在整个正畸锥体细胞EPSP / EPSC中均存在GABAA介导的影响。药理分离的单突触IPSP,IPSC和抑制电导(g GABAA)动力学的比较显示,g GABAA的动力学最快。在单突触g GABAA和诱发的EPSP / EPSC的上升阶段之间观察到紧密的时间重叠。 g GABAA的发作与EPSP / EPSC的发作同时发生或在其之前。 4.前馈IPSP的发生与成对记录中> 80%的锥体细胞EPSP的上升阶段相吻合。最快的前馈抑制反应与诱发的激发几乎完全重叠。 5.在诱发的EPSP的上升阶段并未发生复发性IPSP的发作,而是在锥体细胞EPSP的峰值之后> 3.0 ms发作。 6.在刺激强度低于伴随记录的锥体细胞中引起EPSPs的阈值时观察到正统诱发的中间神经元尖峰。最弱的兴奋性输入对前馈抑制反应的激活,以及前馈抑制和诱发的兴奋之间存在较大的时间重叠,提示原位CA1中的任何兴奋性输入均受快速突触抑制的有效控制。

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