Pollak George D, Burger R Michael, Park Thomas J, Klug Achim, Bauer Eric E
Section of Neurobiology, The University of Texas at Austin, Austin, TX 78731, USA.
Hear Res. 2002 Jun;168(1-2):60-78. doi: 10.1016/s0378-5955(02)00362-3.
This review is concerned with the operation of circuits in the central auditory system, how they transform response features and what functional significance may be attributed to those transformations. We focus on the role that GABAergic inhibition plays in processing interaural intensity disparities (IIDs), the principal cues for localizing high frequencies, and the transformations of IID coding that occur between the superior olivary complex and the inferior colliculus (IC). IIDs are coded by excitatory-inhibitory (EI) cells, so called because they are excited by one ear and inhibited by the other. EI neurons are first created in the lateral superior olive (LSO), but they also dominate the dorsal nucleus of the lateral lemniscus (DNLL) and regions of the IC. The three nuclei are intimately linked through a complex arrangement of excitatory and inhibitory connections. One of these is a crossed excitatory projection from the LSO to both the DNLL and IC. The binaural properties of EI neurons in LSO, DNLL and IC appear strikingly similar, suggesting that the EI properties created in the LSO are simply imposed on the DNLL and IC through the crossed excitatory projections. Recent studies support the idea that EI properties created in lower centers are imposed on some IC cells. However, other studies show that the circuitry linking LSO, DNLL and IC generates a number of response transformations in many IC cells. These transformations include marked changes in EI properties with stimulus duration, the generation of highly focused spatial receptive fields, shifts in sensitivity to IIDs, and the de novo creation of the EI response property. All of these transformations are produced by inhibitory innervation of the IC. An additional emergent property is also imposed on IC cells that receive GABAergic innervation from the DNLL. That property is a change in the binaural features of the IC cell, a change produced by the reception of an earlier sound whose IID is strongly excitatory to the IC cell. We illustrate each of these transformations, propose circuitry that could account for the observed properties and suggest some functional relevance for each. In the final section, we discuss some of the inherent uncertainties associated with attributing functional consequences to response features and then consider whether the transformations found in some mammals are species-specific or are universal features of all mammals.
本综述关注中枢听觉系统中神经回路的运作、它们如何转换反应特征以及这些转换可能具有的功能意义。我们重点探讨γ-氨基丁酸能抑制在处理双耳强度差异(IIDs)中的作用,IIDs是定位高频声音的主要线索,以及在橄榄上复合体和下丘(IC)之间发生的IID编码转换。IID由兴奋性-抑制性(EI)细胞编码,之所以这样称呼是因为它们被一只耳朵兴奋而被另一只耳朵抑制。EI神经元首先在外侧上橄榄核(LSO)中产生,但它们在外侧丘系背核(DNLL)和下丘区域也占主导地位。这三个核团通过复杂的兴奋性和抑制性连接紧密相连。其中之一是从LSO到DNLL和IC的交叉兴奋性投射。LSO、DNLL和IC中EI神经元的双耳特性看起来非常相似,这表明在LSO中产生的EI特性只是通过交叉兴奋性投射强加给DNLL和IC。最近的研究支持这样的观点,即较低中枢产生的EI特性被强加给一些下丘细胞。然而,其他研究表明,连接LSO、DNLL和IC的神经回路在许多下丘细胞中产生了一些反应转换。这些转换包括EI特性随刺激持续时间的显著变化、高度聚焦的空间感受野的产生、对IID敏感性的变化以及EI反应特性的重新产生。所有这些转换都是由下丘的抑制性神经支配产生的。另一个新出现的特性也被强加给接受来自DNLL的γ-氨基丁酸能神经支配的下丘细胞。该特性是下丘细胞双耳特征的变化,这种变化是由接收一个其IID对下丘细胞有强烈兴奋性的更早声音所产生的。我们阐述了这些转换中的每一种,提出了能够解释所观察到特性的神经回路,并为每种转换提出了一些功能相关性。在最后一部分,我们讨论了将功能后果归因于反应特征所固有的一些不确定性,然后考虑在一些哺乳动物中发现的这些转换是物种特异性的还是所有哺乳动物的普遍特征。