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氟西汀对慢性不可预测应激诱导的抑郁模型大鼠海马区少突胶质细胞的影响。

The effects of fluoxetine on oligodendrocytes in the hippocampus of chronic unpredictable stress-induced depressed model rats.

作者信息

Wang Jin, Luo Yanmin, Tang Jing, Liang Xin, Huang Chunxia, Gao Yuan, Qi Yingqiang, Yang Chunmao, Chao FengLei, Zhang Yang, Tang Yong

机构信息

Department of Histology and Embryology, Chongqing Medical University, Chongqing, People's Republic of China.

Laboratory of Stem Cells and Tissue Engineering, Chongqing Medical University, Chongqing, People's Republic of China.

出版信息

J Comp Neurol. 2020 Oct 15;528(15):2583-2594. doi: 10.1002/cne.24914. Epub 2020 Apr 11.

Abstract

Depression is a mental illness which is harmful seriously to the society. This study investigated the effects of fluoxetine on the CNPase oligodendrocytes in hippocampus of the depressed rats to explore the new target structure of antidepressants. Male Sprague-Dawley rats were used to build chronic unpredictable stress (CUS) depressed model of rats. Then, the depressed rats were divided into the CUS standard group and the CUS + fluoxetine (CUS/FLX) group. The CUS/FLX group was treated with fluoxetine at dose of 5 mg/(kg·d) from the fifth week to seventh week. After 7 weeks CUS intervention, the sucrose preference of the CUS standard group was significantly lower than that of the control group and the CUS/FLX group. The stereological results showed that the total number of the CNPase cells in the CA1, CA3, and DG subfield of the hippocampus in the CUS standard group were significantly decreased, when compared with the CNPase cells in the control group. However, the total number of the CNPase cells in the CA1 and CA3 subfield of the hippocampus in the CUS standard group was significantly decreased when it compared with CNPase cells in the CUS/FLX group. Therefore, fluoxetine might prevent the loss of CNPase oligodendrocytes in CA1 and CA3 subfields of hippocampus of the depressed rats. The oligodendrocytes in hippocampus may play an important role in the pathogenesis of depression. The current result might provide structural basis for the future studies that search for new antidepressant strategies.

摘要

抑郁症是一种对社会有严重危害的精神疾病。本研究调查了氟西汀对抑郁大鼠海马中CNPase少突胶质细胞的影响,以探索抗抑郁药的新靶点结构。采用雄性Sprague-Dawley大鼠建立慢性不可预测应激(CUS)抑郁大鼠模型。然后,将抑郁大鼠分为CUS标准组和CUS + 氟西汀(CUS/FLX)组。CUS/FLX组从第5周开始至第7周,以5 mg/(kg·d)的剂量给予氟西汀治疗。经过7周的CUS干预后,CUS标准组的蔗糖偏好显著低于对照组和CUS/FLX组。体视学结果显示,与对照组的CNPase细胞相比,CUS标准组海马CA1、CA3和DG亚区的CNPase细胞总数显著减少。然而,与CUS/FLX组的CNPase细胞相比,CUS标准组海马CA1和CA3亚区的CNPase细胞总数显著减少。因此,氟西汀可能预防抑郁大鼠海马CA1和CA3亚区CNPase少突胶质细胞的丢失。海马中的少突胶质细胞可能在抑郁症的发病机制中起重要作用。目前的结果可能为未来寻找新的抗抑郁策略的研究提供结构基础。

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