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幼年泰耶普大鼠在海马体背侧区域的树突分支较短,但没有空间学习障碍。

Juvenile Taiep rats have shorter dendritic trees in the dorsal field of the hippocampus without spatial learning disabilities.

作者信息

Silva-Gómez Adriana B, Bravo-Duran Dolores A, Eguibar Jose R, Cortes Carmen

机构信息

Faculty of Biological Sciences, Benemérita Universidad Autónoma de Puebla, México.

Institute of Physiology, Benemérita Universidad Autónoma de Puebla, México.

出版信息

Synapse. 2018 Jun;72(6):e22024. doi: 10.1002/syn.22024. Epub 2018 Feb 28.

Abstract

Myelin mutant taiep rats show a progressive demyelination in the central nervous system due to an abnormal accumulation of microtubules in the cytoplasm and the processes on their oligodendrocytes. Demyelination is associated with electrophysiological alterations and the mutant had a progressive astrocytosis. The illness is associated with change in cytokine levels and in the expression of different nitric oxide synthase and concomitantly lipoperoxidation in several areas of the brain. However, until now there has been no detailed anatomical analysis of neurons in this mutant. The aim of this study was to analyze the dendritic morphology in the hippocampus using Golgi-Cox staining and spatial memory through Morris water maze test in young adult (3 months old) taiep rats and compare them with normal Sprague-Dawley. Our results showed that taiep rats have altered dendritic tree morphology in pyramidal neurons in the CA1 field of the hippocampus, but not in the CA3 region. These morphological changes did not produce a concomitant deficit in spatial memory acquisition or recall at this early stage of the disease. Our results suggest that impairment of dendritic morphology in the CA1 field of the hippocampus is a landmark of the pathology of this progressive multiple sclerosis model.

摘要

髓磷脂突变的泰耶普大鼠由于少突胶质细胞胞质及其突起中微管异常积聚,在中枢神经系统中表现出进行性脱髓鞘。脱髓鞘与电生理改变有关,且该突变体存在进行性星形细胞增生。该疾病与细胞因子水平变化、不同一氧化氮合酶的表达变化以及大脑多个区域的脂质过氧化有关。然而,迄今为止,尚未对该突变体中的神经元进行详细的解剖学分析。本研究的目的是使用高尔基-考克斯染色法分析年轻成年(3个月大)泰耶普大鼠海马体中的树突形态,并通过莫里斯水迷宫试验分析其空间记忆,然后将它们与正常的斯普拉格-道利大鼠进行比较。我们的结果表明,泰耶普大鼠海马体CA1区锥体细胞的树突形态发生了改变,但CA3区没有。在疾病的这个早期阶段,这些形态变化并没有在空间记忆获取或回忆方面产生相应的缺陷。我们的结果表明,海马体CA1区树突形态的损伤是这种进行性多发性硬化模型病理学的一个标志。

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