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听觉中脑中spectrotemporal 整合的基础电路。

Circuitry underlying spectrotemporal integration in the auditory midbrain.

机构信息

Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, Ohio 44272, USA.

出版信息

J Neurosci. 2011 Oct 5;31(40):14424-35. doi: 10.1523/JNEUROSCI.3529-11.2011.

DOI:10.1523/JNEUROSCI.3529-11.2011
PMID:21976527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3226782/
Abstract

Combination sensitivity in central auditory neurons is a form of spectrotemporal integration in which excitatory responses to sounds at one frequency are facilitated by sounds within a distinctly different frequency band. Combination-sensitive neurons respond selectively to acoustic elements of sonar echoes or social vocalizations. In mustached bats, this response property originates in high-frequency representations of the inferior colliculus (IC) and depends on low and high frequency-tuned glycinergic inputs. To identify the source of these inputs, we combined glycine immunohistochemistry with retrograde tract tracing. Tracers were deposited at high-frequency (>56 kHz), combination-sensitive recording sites in IC. Most glycine-immunopositive, retrogradely labeled cells were in ipsilateral ventral and intermediate nuclei of the lateral lemniscus (VNLL and INLL), with some double labeling in ipsilateral lateral and medial superior olivary nuclei (LSO and MSO). Generally, double-labeled cells were in expected high-frequency tonotopic areas, but some VNLL and INLL labeling appeared to be in low-frequency representations. To test whether these nuclei provide low frequency-tuned input to the high-frequency IC, we combined retrograde tracing from IC combination-sensitive sites with anterograde tracing from low frequency-tuned sites in the anteroventral cochlear nucleus (AVCN). Only VNLL and INLL contained retrogradely labeled cells near (≤50 μm) anterogradely labeled boutons. These cells likely receive excitatory low-frequency input from AVCN. Results suggest that combination-sensitive facilitation arises through convergence of high-frequency glycinergic inputs from VNLL, INLL, or MSO and low-frequency glycinergic inputs from VNLL or INLL. This work establishes an anatomical basis for spectrotemporal integration in the auditory midbrain and a functional role for monaural nuclei of the lateral lemniscus.

摘要

中枢听觉神经元的组合敏感性是一种频谱时间整合形式,其中对一个频率的声音的兴奋性反应被明显不同频率带内的声音所促进。组合敏感神经元对声纳回波或社会发声的声学元素有选择性反应。在髭蝠中,这种反应特性起源于下丘(IC)的高频表示,并且依赖于低频和高频调谐的甘氨酸能输入。为了确定这些输入的来源,我们将甘氨酸免疫组织化学与逆行束追踪相结合。示踪剂被沉积在高频(> 56 kHz)、组合敏感记录部位的 IC 中。大多数甘氨酸免疫阳性、逆行标记的细胞位于同侧腹侧和中间外侧丘系核(VNLL 和 INLL),在同侧外侧和内侧上橄榄核(LSO 和 MSO)中有一些双标记。一般来说,双标记细胞位于预期的高频音位区,但一些 VNLL 和 INLL 标记似乎位于低频表示中。为了测试这些核是否为高频 IC 提供低频调谐输入,我们将来自 IC 组合敏感部位的逆行追踪与来自前腹侧耳蜗核(AVCN)低频调谐部位的顺行追踪相结合。只有 VNLL 和 INLL 在(≤50 μm)顺行标记的末梢附近含有逆行标记的细胞。这些细胞可能从前庭耳蜗核(AVCN)接收兴奋性低频输入。结果表明,组合敏感促进是通过来自 VNLL、INLL 或 MSO 的高频甘氨酸能输入和来自 VNLL 或 INLL 的低频甘氨酸能输入的会聚而产生的。这项工作为听觉中脑的频谱时间整合建立了一个解剖学基础,并为外侧丘系的单耳核的功能作用奠定了基础。

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本文引用的文献

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