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猫听觉神经的无髓鞘轴突。

Unmyelinated axons of the auditory nerve in cats.

作者信息

Ryugo D K, Dodds L W, Benson T E, Kiang N Y

机构信息

Department of Anatomy and Cellular Biology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Comp Neurol. 1991 Jun 8;308(2):209-23. doi: 10.1002/cne.903080208.

Abstract

This paper describes some central terminations of type II spiral ganglion neurons as labeled by extracellular injections of horseradish peroxidase (HRP) into the auditory nerve of cats. After histological processing with diaminobenzidine, both thick (2-4 microns) and thin (0.5 microns) fibers of the auditory nerve were stained. Whenever traced, thick fibers always originated from type I spiral ganglion neurons and thin fibers always from type II ganglion neurons. Because the labeling of type II axons faded as fibers projected into the cochlear nucleus, this report is limited to regions of the ventral cochlear nucleus near the auditory nerve root. The central axons of type II neurons are unmyelinated, have simple yet variable branching patterns in the cochlear nucleus, and form both en passant and terminal swellings. Under the light microscope, most swellings are located in the neuropil but they are also found in the vicinity of cell bodies, nodes of Ranvier of type I axons, and blood vessels. Eighteen en passant swellings in the neuropil were located by light microscopy and resectioned for electron microscopy; two of these swellings exhibited ultrastructural features characteristic of chemical synapses. The data indicate that inputs from outer hair cells might be able to influence auditory processing in the cochlear nucleus through type II primary neurons.

摘要

本文描述了通过向猫的听神经细胞外注射辣根过氧化物酶(HRP)标记的II型螺旋神经节神经元的一些中枢终末。用二氨基联苯胺进行组织学处理后,听神经的粗纤维(2 - 4微米)和细纤维(0.5微米)均被染色。只要进行追踪,粗纤维总是起源于I型螺旋神经节神经元,细纤维总是起源于II型神经节神经元。由于II型轴突的标记在纤维投射到蜗神经核时会逐渐消失,本报告仅限于靠近听神经根的蜗神经腹侧核区域。II型神经元的中枢轴突无髓鞘,在蜗神经核中具有简单但多变的分支模式,并形成中途膨大及终末膨大。在光学显微镜下,大多数膨大位于神经毡中,但也可在细胞体附近、I型轴突的郎飞结以及血管附近发现。通过光学显微镜定位了神经毡中的18个中途膨大,并对其进行切片用于电子显微镜观察;其中两个膨大表现出化学突触的超微结构特征。数据表明,外毛细胞的输入可能能够通过II型初级神经元影响蜗神经核中的听觉处理。

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