首页> 美国卫生研究院文献>Biomolecules Therapeutics >Spinosin a C-Glucosylflavone from Zizyphus jujuba var. spinosa Ameliorates Aβ1–42 Oligomer-Induced Memory Impairment in Mice
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Spinosin a C-Glucosylflavone from Zizyphus jujuba var. spinosa Ameliorates Aβ1–42 Oligomer-Induced Memory Impairment in Mice

机译:Spinosin一种C-葡萄糖基黄酮得自枣木(Zizyphus jujuba var)。 spinosa改善Aβ1-42寡聚物诱导的小鼠记忆障碍

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摘要

Alzheimer’s disease (AD) is a neurodegenerative disorder associated with progressive memory loss and neuronal cell death. Although numerous previous studies have been focused on disease progression or reverse pathological symptoms, therapeutic strategies for AD are limited. Alternatively, the identification of traditional herbal medicines or their active compounds has received much attention. The aims of the present study were to characterize the ameliorating effects of spinosin, a C-glucosylflavone isolated from Zizyphus jujuba var. spinosa, on memory impairment or the pathological changes induced through amyloid-β1–42 oligomer (AβO) in mice. Memory impairment was induced by intracerebroventricular injection of AβO (50 μM) and spinosin (5, 10, and 20 mg/kg) was administered for 7 days. In the behavioral tasks, the subchronic administration of spinosin (20 mg/kg, p.o.) significantly ameliorated AβO-induced cognitive impairment in the passive avoidance task or the Y-maze task. To identify the effects of spinosin on the pathological changes induced through AβO, immunohistochemistry and Western blot analyses were performed. Spinosin treatment also reduced the number of activated microglia and astrocytes observed after AβO injection. In addition, spinosin rescued the AβO-induced decrease in choline acetyltransferase expression levels. These results suggest that spinosin ameliorated memory impairment induced through AβO, and these effects were regulated, in part, through neuroprotective activity via the anti-inflammatory effects of spinosin. Therefore, spinosin might be a useful agent against the amyloid b protein-induced cognitive dysfunction observed in AD patients.
机译:阿尔茨海默氏病(AD)是与进行性记忆丧失和神经元细胞死亡相关的神经退行性疾病。尽管先前的许多研究都集中在疾病进展或逆向病理症状上,但是AD的治疗策略仍然有限。替代地,传统草药或其活性化合物的鉴定已引起广泛关注。本研究的目的是表征刺糖多孢菌素的改善作用,刺糖多孢菌素是从枣木(Zizyphus jujuba var)中分离得到的C-葡萄糖基黄酮。糖对小鼠的记忆力减退或淀粉样蛋白1-42寡聚物(AβO)引起的病理变化。脑室内注射AβO(50μM)诱发记忆力减退,并给予spinosin(5、10和20 mg / kg)7天。在行为任务中,亚慢性给药多杀菌素(20 mg / kg,p.o。)在被动回避任务或Y迷宫任务中可显着改善AβO诱导的认知障碍。为了确定多杀菌素对AβO引起的病理变化的影响,进行了免疫组织化学和蛋白质印迹分析。注射AβO后,刺糖多孢菌素处理还减少了活化的小胶质细胞和星形胶质细胞的数量。此外,斯皮诺菌素挽救了AβO诱导的胆碱乙酰转移酶表达水平的下降。这些结果表明,多杀菌素改善了由AβO引起的记忆障碍,并且这些作用部分地通过多杀菌素的抗炎作用通过神经保护活性来调节。因此,Spinosin可能是对抗AD患者中淀粉样蛋白B诱导的认知功能障碍的有用药物。

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