Department of Physiology, School of Medicine of Ribeirão Preto, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, SP 14019-900, Brazil.
Hear Res. 2019 May;376:33-46. doi: 10.1016/j.heares.2018.12.011. Epub 2018 Dec 26.
The auditory part of the brainstem is composed of several nuclei specialized in the computation of the different spectral and temporal features of the sound before it reaches the higher auditory regions. There are a high diversity of neuronal types in these nuclei, many with remarkable electrophysiological and synaptic properties unique to these structures. This diversity reflects specializations necessary to process the different auditory signals in order to extract precisely the acoustic information necessary for the auditory perception by the animal. Low threshold Kv1 channels and HCN channels are expressed in neurons that use timing clues for auditory processing, like bushy and octopus cells, in order to restrict action potential firing and reduce input resistance and membrane time constant. Kv3 channels allow principal neurons of the MNTB and pyramidal DCN neurons to fire fast trains of action potentials. Calcium channels on cartwheel DCN neurons produce complex spikes characteristic of these neurons. Calyceal synapses compensate the low input resistance of bushy and principal neurons of the MNTB by releasing hundreds of glutamate vesicles resulting in large EPSCs acting in fast ionotropic glutamate receptors, in order to reduce temporal summation of synaptic potentials, allowing more precise correspondence of pre- and post-synaptic potentials, and phase-locking. Pre-synaptic calyceal sodium channels have fast recovery from inactivation allowing extremely fast trains of action potential firing, and persistent sodium channels produce spontaneous activity of fusiform neurons at rest, which expands the dynamic range of these neurons. The unique combinations of different ion channels, ionotropic receptors and synaptic structures create a unique functional diversity of neurons extremely adapted to their complex functions in the auditory processing.
脑桥的听觉部分由几个专门用于计算声音不同频谱和时频特征的核组成,这些特征在声音到达更高的听觉区域之前就已经被计算出来了。这些核中存在着高度多样化的神经元类型,其中许多具有独特的电生理和突触特性,这些特性是这些结构所特有的。这种多样性反映了为处理不同的听觉信号而进行的专门化,以便精确提取动物听觉感知所需的声学信息。低阈值 Kv1 通道和 HCN 通道在使用定时线索进行听觉处理的神经元中表达,如篮状细胞和章鱼细胞,以限制动作电位的发放,并降低输入电阻和膜时间常数。Kv3 通道允许 MNTB 的主要神经元和 DCN 锥体神经元快速发射动作电位。DCN 神经元上的钙通道产生这些神经元特有的复杂 spikes。杯状突触通过释放数百个谷氨酸囊泡来补偿篮状细胞和 MNTB 的主要神经元的低输入电阻,从而产生作用于快速离子型谷氨酸受体的大 EPSC,以减少突触电位的时间总和,允许更精确的前后突触电位对应,并锁定相位。前突触杯状钠通道具有快速恢复失活的特性,允许极快的动作电位发射,而持续钠通道在休息时产生梭形神经元的自发性活动,这扩展了这些神经元的动态范围。不同离子通道、离子型受体和突触结构的独特组合,为神经元创造了独特的功能多样性,使它们极其适应听觉处理中的复杂功能。