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甲状腺功能减退成年大鼠听觉胼胝体连接的组织学研究

Organization of auditory callosal connections in hypothyroid adult rats.

作者信息

Berbel P, Guadaño-Ferraz A, Martínez M, Quiles J A, Balboa R, Innocenti G M

机构信息

Departament d'Histologia, Facultat de Medicina, Universitat d'Alacant, Spain.

出版信息

Eur J Neurosci. 1993 Nov 1;5(11):1465-78. doi: 10.1111/j.1460-9568.1993.tb00214.x.

Abstract

Callosal connections were studied with tracers (horseradish peroxidase (HRP) and wheat germ agglutinin-horseradish peroxidase (WGA-HRP)) in normal rats and rats deprived of thyroid hormones with methimazole (Sigma) since embryonic day 14 and thyroidectomized at postnatal day 6. In hypothyroid rats, the auditory areas, in particular the primary auditory area, showed cytoarchitectonic changes including blurred lamination and decrease in the size of layer V pyramidal neurons. In control rats, callosally-projecting neurons were found between layers II and VI with a peak in layer III and upper layer IV. In hypothyroid rats, labelled neurons were found between layers IV and VI with two peaks corresponding to layer IV and upper layer V, and in upper layer VI. Quantitative analysis of radial distribution of callosally-projecting neurons confirmed their shift to infragranular layers in hypothyroid rats. Three-dimensional reconstructions showed a more continuous tangential distribution of callosally-projecting neurons in hypothyroid rats which may be due to the maintenance of a juvenile 'exuberant' pattern of projections. These changes in cortical connectivity may be relevant for understanding epilepsy and mental retardation associated with early hypothyroidism in humans and to clarify basic mechanisms of cortical development.

摘要

在正常大鼠以及自胚胎第14天起用甲巯咪唑(西格玛公司)剥夺甲状腺激素并在出生后第6天进行甲状腺切除的大鼠中,使用示踪剂(辣根过氧化物酶(HRP)和麦胚凝集素 - 辣根过氧化物酶(WGA - HRP))研究胼胝体连接。在甲状腺功能减退的大鼠中,听觉区域,特别是初级听觉区域,显示出细胞结构变化,包括分层模糊和V层锥体神经元大小减小。在对照大鼠中,胼胝体投射神经元位于II层和VI层之间,在III层和IV层上部达到峰值。在甲状腺功能减退的大鼠中,标记神经元位于IV层和VI层之间,在IV层和V层上部以及VI层上部有两个峰值。对胼胝体投射神经元径向分布的定量分析证实它们在甲状腺功能减退的大鼠中向颗粒下层转移。三维重建显示,甲状腺功能减退的大鼠中胼胝体投射神经元的切向分布更连续,这可能是由于维持了幼年“旺盛”的投射模式。皮质连接性的这些变化可能与理解人类早期甲状腺功能减退相关的癫痫和智力迟钝有关,并有助于阐明皮质发育的基本机制。

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