首页> 外文期刊>Journal of immunology research. >Neuroprotective Effects of Asparagus officinalis Stem Extract in Transgenic Mice Overexpressing Amyloid Precursor Protein
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Neuroprotective Effects of Asparagus officinalis Stem Extract in Transgenic Mice Overexpressing Amyloid Precursor Protein

机译:芦笋Officinalis干提取物在转基因小鼠过表达淀粉样蛋白前体蛋白的转基因小鼠中的神经保护作用

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To mimic Alzheimer’s disease, transgenic mice overexpressing the amyloid precursor protein (APP) were used in this study. We hypothesize that the neuroprotective effects of ETAS?50, a standardized extract of Asparagus officinalis stem produced by Amino Up Co., Ltd. (Sapporo, Japan), are linked to the inhibition of the apoptosis cascade through an enhancement of the stress-response proteins: heat shock proteins (HSPs). APP-overexpressing mice (double-transgenic APP and PS1 mouse strains with a 129s6 background), ages 6-8 weeks old, and weighing 20-24 grams were successfully bred in our laboratory. The animals were divided into 5 groups. APP-overexpressing mice and wild-type (WT) mice were pretreated with ETAS?50 powder (50% elemental ETAS and 50% destrin) at 200?mg/kg and 1000?mg/kg body weight. Saline, the vehicle for ETAS?50, was administered in APP-overexpressing mice and WT mice. ETAS?50 and saline were administered by gavage daily for 1 month. Cognitive assessments, using the Morris Water Maze, demonstrated that memory was recovered following ETAS?50 treatment as compared to nontreated APP mice. At euthanization, the brain was removed and HSPs, amyloid β , tau proteins, and caspase-3 were evaluated through immunofluorescence staining with the appropriate antibodies. Our data indicate that APP mice have cognitive impairment along with elevated amyloid β , tau proteins, and caspase-3. ETAS?50 restored cognitive function in these transgenic mice, increased both HSP70 and HSP27, and attenuated pathogenic level of amyloid β , tau proteins, and caspsase-3 leading to neuroprotection. Our results were confirmed with a significant increase in HSP70 gene expression in the hippocampus.
机译:为了模仿阿尔茨海默病的疾病,在本研究中使用过表达淀粉样蛋白前体蛋白(APP)的转基因小鼠。我们假设ETAS的神经保护作用(ETAS的神经保护效果,由氨基Up Co.,Ltd。(札幌,日本)产生的芦笋Officinalis茎的标准化提取物,通过增强应力反应来与凋亡级联的抑制相关联蛋白质:热休克蛋白(HSP)。应用程序过度抑制小鼠(双转基因APP和PS1鼠标菌株129S6背景),在我们的实验室中成功地培育6-8周龄6-8周龄,重达20-24克。将动物分成5组。用ETAS?50次粉末(50%元素ETAS和50%DATRIN)预处理APP-过度抑制小鼠和野生型(WT)小鼠,在200×mg / kg和1000μg/ kg体重。盐水,etaSα50的车辆在应用过度抑制小鼠和WT小鼠中施用。 ETAS?50和盐水每天施用1个月。使用莫里斯水迷宫的认知评估证明了与非生成的APP小鼠相比,ETASα50治疗后记忆恢复。在制方案化时,通过用适当抗体的免疫荧光染色来评估大脑并除去HSP,淀粉样蛋白β,Tau蛋白和Caspase-3。我们的数据表明,应用小鼠具有认知障碍以及升高的淀粉样蛋白β,Tau蛋白和Caspase-3。 etas?50恢复在这些转基因小鼠中的认知功能,增加了Hsp70和Hsp27,并衰减了淀粉样蛋白β,tau蛋白和皮甲酶-3的致病水平,导致神经保护蛋白酶-3。我们的结果被证实在海马中的HSP70基因表达显着增加。

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