首页> 美国卫生研究院文献>Aging (Albany NY) >Soy isoflavones ameliorate the cognitive dysfunction of Goto-Kakizaki rats by activating the Nrf2-HO-1 signalling pathway
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Soy isoflavones ameliorate the cognitive dysfunction of Goto-Kakizaki rats by activating the Nrf2-HO-1 signalling pathway

机译:大豆异黄酮通过激活NRF2-HO-1信号通路来改善Goto-Kakizaki大鼠的认知功能障碍

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摘要

Soy isoflavones (SIF) are soybean phytochemicals that are considered to be biologically active components that protect from neurodegenerative diseases. In this study, the therapeutic effect of SIF was evaluated in a diabetic Goto-Kakizaki (GK) rat model. Twenty male GK rats were randomly divided into diabetes mellitus (DM) model group and SIF+DM group (n=10 in each group). Twenty age-matched male Wistar rats were randomly divided into control group (CON group) and CON+SIF group, with 10 rats in each group. The learning and memory functions of the animals were determined by the Morris water maze (MWM) test. Hematoxylin-eosin staining (HE) was performed to examine pyramidal neuron loss in the CA1 area of the hippocampus. Markers of oxidative stress (OS) were measured to evaluate oxidative stress-mediated injury. RT-PCR and western blotting were used to analyze the expression of nuclear factorerythroid2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1) and NAD(P)H dehydrogenase quinone1 (NQO1). Treatment with SIF for 4 weeks alleviated the cognitive dysfunction of the GK rats as determined by the MWM test. Moreover, SIF treatment also reduced diabetes-related oxidative reactions. In addition, SIF enhanced the expression of Nrf2, HO-1 and NQO1, suggesting a potential antioxidation mechanism for the effect of SIF. These findings suggest that SIF can be considered candidates for inhibiting the progression of diabetes-induced cognitive dysfunction, provide novel insights into the antioxidant effect of SIF and further strengthen the link between oxidative stress and diabetes.
机译:大豆异黄酮(SIF)是大豆植物化学物质,被认为是免受神经变性疾病的生物活性组分。在该研究中,SIF的治疗效果在糖尿病Goto-kakizaki(GK)大鼠模型中评价。将20只雄性GK大鼠随机分为糖尿病(DM)模型组和SIF + DM组(在每组中N = 10)。将20岁匹配的雄性Wistar大鼠随机分为对照组(CON组)和Con + SIF组,每组10只大鼠。动物的学习和记忆功能由Morris水迷宫(MWM)试验确定。进行苏木精 - 曙红染色(HE)以检查海马CA1面积的金字塔神经元损失。测量氧化应激(OS)的标记以评估氧化应激介导的损伤。 RT-PCR和Western印迹用于分析核因子核心偶别2相关因子2(NRF2),血红素氧基氨基酶-1(HO-1)和NAD(P)H脱氢酶醌1(NQO1)的表达。用SIF处理4周的处理减轻了通过MWM测试测定的GK大鼠的认知功能障碍。此外,SIF治疗还降低了糖尿病相关的氧化反应。此外,SIF增强了NRF2,HO-1和NQO1的表达,表明SIF的效果的潜在抗氧化机制。这些研究结果表明,SIF可以被认为是抑制糖尿病诱导的认知功能障碍进展的候选者,为SIF的抗氧化效果提供了新的见解,进一步加强了氧化应激和糖尿病之间的联系。

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