hascs静脉给药后阿尔茨海默病大鼠模型的组织学和行为学改变

Thrita Pub Date : 2020-01-14 DOI:10.5812/thrita.99975
Milad Kazemiha, A. Sarveazad, F. Moradi, Farnaz Ramezanpour, M. Vosoogh, Maryam Doshmanziari, Marjan Shariatpanahi, M. Eftekharzadeh
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引用次数: 2

摘要

背景:阿尔茨海默病(AD)是一种进行性认知障碍,通常与年龄有关。尽管对这种疾病已经有了大量的研究,但仍然缺乏可靠的治疗方法。淀粉样蛋白- β (A β)肽在阿尔茨海默病的神经病理中起重要作用。干细胞疗法通过改善神经退行性疾病的神经系统提供治疗。人脂肪源性干细胞(hADSCs)由于其安全性、高促增殖潜力和易于分离而成为最合适的干细胞来源。目的:本研究旨在评估静脉给药hascs对AD大鼠模型的组织学和行为学改变。方法:选用雄性大鼠32只,分为4组:对照组、假手术组、AD大鼠模型组和hadscs治疗组。我们使用Morris水迷宫(MWM)评估行为变化,尼氏染色测定组织学研究。结果:本研究通过行为学和组织学分析证实了AD模型。行为学结果显示,在AD大鼠模型中注射hADSCs后,空间记忆得到改善,而在目标象限中停留的时间明显高于AD大鼠模型组。另一方面,通过尼氏染色分析,hadscs处理组的死细胞数量明显减少。结论:我们的研究结果表明,hascs可以转移到大脑中,改善AD大鼠模型的记忆和神经元损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histological and Behavioral Alterations Following hADSCs Intravenous Administration in Alzheimer’s Rat Model
Background: Alzheimer’s disease (AD) is a progressive cognitive disorder that is generally age-related. Although there has been great research focusing on this disease, there is still a lack of reliable therapeutic methods. Amyloid- β (A β ) peptide has a critical function in neuropathology of AD. Stem cell therapy provides treatment by improving the neuronal system in neurodegenerative disorders. Human adipose-derived stem cells (hADSCs) are the most appropriate sources of stem cells due to their safety, high pro-liferative potential, and easy isolation. Objectives: Thepresentstudywasdesignedtoevaluatethehistologicalandbehavioralalterationsafterintravenousadministration of hADSCs in the AD rat model. Methods: In this study, 32 male rats were used in four groups, as follows: control, sham, AD rat model, and hADSCs-treated group. We used Morris Water Maze (MWM) for evaluating behavioral changes and Nissl staining for determining the histological studies. Results: In this study, the AD model was confirmed by behavioral and histological analysis. Behavioral results showed that the spatial memory improved after hADSCs injection in the AD rat model while the time spent in the target quadrant was significantly higher in the hADSCs-treated group than in the AD rat model group. On the other hand, the number of dead cells significantly decreased in the hADSCs-treated group as analyzed by Nissl staining. Conclusions: Our findings revealed that hADSCs could transfer into the brain and improve memory and neuronal damage in the AD rat model.
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