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Possible mechanisms of lycopene amelioration of learning and memory impairment in rats with vascular dementia

机译:植物痴呆大鼠学习和记忆障碍的可能机制

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Oxidative stress is involved in the pathogenesis of vascular dementia. Studies have shown that lycopene can significantly inhibit oxidative stress; therefore, we hypothesized that lycopene can reduce the level of oxidative stress in vascular dementia. A vascular dementia model was established by permanent bilateral ligation of common carotid arteries. The dosage groups were treated with lycopene (50, 100 and 200 mg/kg) every other day for 2 months. Rats without bilateral carotid artery ligation were prepared as a sham group. To test the ability of learning and memory, the Morris water maze was used to detect the average escape latency and the change of search strategy. Hematoxylin-eosin staining was used to observe changes of hippocampal neurons. The levels of oxidative stress factors, superoxide dismutase and malondialdehyde, were measured in the hippocampus by biochemical detection. The levels of reactive oxygen species in the hippocampus were observed by dihydroethidium staining. The distribution and expression of oxidative stress related protein, neuron-restrictive silencer factor, in hippocampal neurons were detected by immunofluorescence histochemistry and western blot assays. After 2 months of drug administration, (1) in the model group, the average escape latency was longer than that of the sham group, and the proportion of straight and tend tactics was lower than that of the sham group, and the hippocampal neurons were irregularly arranged and the cytoplasm was hyperchromatic. (2) The levels of reactive oxygen species and malondialdehyde in the hippocampus of the model group rats were increased, and the activity of superoxide dismutase was decreased. (3) Lycopene (50, 100 and 200 mg/kg) intervention improved the above changes, and the lycopene 100 mg/kg group showed the most significant improvement effect. (4) Neuron-restrictive silencer factor expression in the hippocampus was lower in the sham group and the lycopene 100 mg/kg group than in the model group. (5) The above data indicate that lycopene 100 mg/kg could protect against the learning-memory ability impairment of vascular dementia rats. The protective mechanism was achieved by inhibiting oxidative stress in the hippocampus. The experiment was approved by the Animal Ethics Committee of Fujian Medical University, China (approval No. 2014-025) in June 2014.
机译:氧化应激参与血管痴呆的发病机制。研究表明,番茄红素可显着抑制氧化应激;因此,我们假设番茄红素可以降低血管痴呆症中氧化应激水平。血管痴呆模型是通过常见的颈动脉的永久性双侧结扎建立。每隔一天用番茄红素(50,100和200mg / kg)处理剂量2个月。没有双侧颈动脉连接的大鼠制备为假组。为了测试学习和记忆能力,莫里斯水迷宫用于检测平均逃生延迟和搜索策略的变化。苏木精 - 曙红染色用于观察海马神经元的变化。通过生物化学检测在海马中测量氧化应激因子,超氧化物歧化酶和丙二醛的水平。通过二氢甲基羟磷酰胺染色观察海马中活性氧物质的水平。通过免疫荧光组织化学和蛋白质印迹测定检测氧化应激相关蛋白质,神经限制沉默因子的分布和表达。在2个月的药物管理后,(1)在模型组中,平均逃生潜伏期比假组的延伸时间长,直率和倾向策略的比例低于假组,并且海马神经元不规则地排列,细胞质是高度的。 (2)模型组大鼠海马中反应性氧物质和丙二醛水平升高,降低过氧化物歧化酶的活性。 (3)番茄红素(50,100和200mg / kg)干预改善了上述变化,番茄红素100mg / kg组显示出最显着的改善效果。 (4)海马中的神经元限制性消声器因子表达在假组和番茄红素100mg / kg组中低于模型组。 (5)上述数据表明番茄红素100mg / kg可以防止血管痴呆大鼠的学习记忆能力损害。通过抑制海马中的氧化应激来实现保护机制。 2014年6月,福建医科大学动物伦理委员会批准了实验批准,2014年6月批准2014-025号。

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