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Inhibitory properties underlying non-monotonic input-output relationship in low-frequency spherical bushy neurons of the gerbil

机译:沙土鼠低频球形丛状神经元中非单调输入-输出关系的抑制特性

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摘要

Spherical bushy cells (SBCs) of the anteroventral cochlear nucleus (AVCN) receive input from large excitatory auditory nerve (AN) terminals, the endbulbs of Held, and mixed glycinergic/GABAergic inhibitory inputs. The latter have sufficient potency to block action potential firing in vivo and in slice recordings. However, it is not clear how well the data from slice recordings match the inhibition in the intact brain and how it contributes to complex phenomena such as non-monotonic rate-level functions (RLF). Therefore, we determined the input-output relationship of a model SBC with simulated endbulb inputs and a dynamic inhibitory conductance constrained by recordings in brain slice preparations of hearing gerbils. Event arrival times from in vivo single-unit recordings in gerbils, where 70% of SBC showed non-monotonic RLF, were used as input for the model. Model output RLFs systematically changed from monotonic to non-monotonic shape with increasing strength of tonic inhibition. A limited range of inhibitory synaptic properties consistent with the slice data generated a good match between the model and recorded RLF. Moreover, tonic inhibition elevated the action potentials (AP) threshold and improved the temporal precision of output functions in a SBC model with phase-dependent input conductance. We conclude that activity-dependent, summating inhibition contributes to high temporal precision of SBC spiking by filtering out weak and poorly timed EPSP. Moreover, inhibitory parameters determined in slice recordings provide a good estimate of inhibitory mechanisms apparently active in vivo.
机译:前腹耳蜗核(AVCN)的球形丛状细胞(SBC)接收来自大型兴奋性听觉神经(AN)末端,Held的终末球以及混合的甘氨酸/ GABA抑制性输入。后者具有足够的效能来阻断体内和切片记录中潜在的动作电位发射。但是,尚不清楚切片记录中的数据与完整大脑中的抑制匹配得如何,以及它如何促成诸如非单调速率水平函数(RLF)之类的复杂现象。因此,我们确定了模拟SBC输入和动态抑制电导的模型SBC的输入-输出关系,该动态抑制电导受听力沙鼠的脑片准备中记录的限制。来自沙鼠体内单个单位记录的事件到达时间(该模型的输入中70%的SBC显示非单调RLF)。模型输出的RLF随音调抑制强度的增加而系统地从单调变为非单调。与切片数据一致的有限范围的抑制性突触特性在模型和记录的RLF之间产生了良好的匹配。此外,在具有相位相关的输入电导的SBC模型中,进补抑制提高了动作电位(AP)阈值并提高了输出功能的时间精度。我们得出的结论是,通过过滤掉弱的和时间差的EPSP,依赖于活动的总抑制作用有助于SBC峰值的高时间精度。此外,在切片记录中确定的抑制参数可以很好地估计表面活性在体内的抑制机制。

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