添加/不添加牛磺酸的脂肪源性间充质干细胞(ADMSCs)在氯化铝诱导的阿尔茨海默病大鼠模型中的治疗潜力

M. Hosney, Alaa Sakraan, Asaad, M., E. F., Emad Elzayat
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引用次数: 0

摘要

阿尔茨海默病(AD)以其进展、神经行为和神经病理特征为特征。脂肪源性间充质干细胞(ADMSCs)先前已被证明在预防几种神经退行性疾病的发病机制中具有潜在作用,因此它被认为是一种有希望的AD再生治疗新方法。牛磺酸被发现增强干细胞的激活和繁殖,产生更高浓度的神经祖细胞和干细胞,并减少激活的小胶质细胞的数量,导致体外炎症下调。本研究旨在探讨ADMSCs加牛磺酸/不加牛磺酸对AD大鼠模型的治疗潜力。计划包括三个连续的阶段:诱导、停药和治疗阶段。50只雄性Wistar大鼠分为两组:对照组(C)和AD模型组。在t型迷宫实验中表现出来的行为变化已经被记录下来。ELISA法测定大鼠脑匀浆及血清中β -淀粉样蛋白水平。用分光光度法测定氧化应激标志物(MDA)、脑和血清抗氧化酶(SOD、GSH和CAT)活性以及血清乙酰胆碱酯酶活性。采用RT-qPCR检测脑内促凋亡基因(p53、Bax)和抗凋亡基因(Bcl2)的表达。脑组织的组织病理学改变也被观察到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Potential of Adipose-Derived Mesenchymal Stem Cells (ADMSCs) with/without Taurine in Aluminum Chloride-Induced Alzheimer's Disease Rat Model
Alzheimer's (AD) of characterized by its progression, neurobehavioral and neuro-pathological characteristics. Adipose-derived mesenchymal stem cells (ADMSCs) have previously proved a potential role in preventing the pathogenesis of several neurodegenerative disorders, so it is regarded as a promising new approach for AD regenerative therapy. Taurine was found to enhance stem cell activation and propagation, yielding a higher concentration of neural progenitors and stem cells, and reducing the number of activated microglia leading to down-regulated inflammation in vitro . The present study aimed to investigate the possible therapeutic potential of ADMSCs with/without taurine in treating the AD rat model. It was planned to include three successive phases: induction, withdrawal, and therapeutic phases. Fifty male Wistar rats were divided into two main groups: control (C) and AD model. Behavioral changes, as manifested by the T-maze experiment, had been recorded. β - amyloid levels had been measured in brain homogenate and serum by ELISA. Oxidative stress marker (MDA), brain and serum antioxidant enzyme activities (SOD, GSH, and CAT) as well serum acetylcholine esterase activity were spectrophotometrically determined. Pro-apoptotic (p53 and Bax) and anti-apoptotic (Bcl2) gene expression in the brain were evaluated using RT-qPCR. The histopathological alterations in brain tissues were also observed.
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