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Annona atemoya leaf extract ameliorates cognitive impairment in amyloid-β injected Alzheimer’s disease-like mouse model

机译:Annona Atemoya Lead提取物改善了淀粉样蛋白-β注入的阿尔茨海默病的鼠标模型中的认知损伤

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摘要

Annona atemoya is a hybrid of Annona squamosa and Annona cherimola that grow in several subtropical or tropical areas such as Florida in the US, Philippines, Cuba, Jamaica, Taiwan, and Jeju in South Korea. We report that the A. atemoya leaves (AAL) have inhibitory effects on the pathogenesis and regulatory mechanisms of Alzheimer’s disease (AD). Ethanol extract of AAL prevented amyloid-β (Aβ) aggregation and increased free radical scavenging activity. In addition, AAL extract exerted protective effects against neuronal cell death in HT22 hippocampal cells. Moreover, oral administration of AAL extract significantly improved memory loss in the passive avoidance task and Y-maze test, as well as downregulated the expression of neuronal markers neuronal nuclei and brain-derived neurotrophic factor in Aβ-injected AD mice. To verify the molecular mechanisms responsible for anti-AD actions of AAL, we conducted the antibody microarray analysis and found that epidermal growth factor receptor/G protein-coupled receptor kinase 2 signaling was activated in neuronal cells and AD-like mouse models. Additionally, quantitative analyses of the six standard compounds using high-performance liquid chromatography revealed that rutin is the most abundant compound of AAL. Furthermore, efficacy analyses of six standard compounds showed that rutin and isoquercitrin had significant inhibitory activity on Aβ aggregation. Taken together with biological activity and the content of compounds, rutin maybe a bioactive compound of AAL in the AD pathogenesis. Overall, our findings provide the first scientific support for the therapeutic effects of AAL in AD and AD-related disorders.
机译:番atemoya是番荔枝程度,在一些亚热带或热带地区,如佛罗里达州,在美国,菲律宾,古巴,牙买加,台湾和济州岛增长番荔枝cherimola的混合体。我们报告说,A. atemoya叶(AAL)对阿尔茨海默病(AD)的发病机制和监管机制的抑制作用。 AAL的乙醇提取物防止淀粉样蛋白β(Aβ)聚集和增加的自由基清除活性。此外,AAL提取物作用于HT22海马细胞对神经细胞死亡的保护作用。此外,AAL提取物的口服给药显著改善Aβ注射AD小鼠在被动回避任务的记忆丧失和Y迷宫测试,以及下调神经元标记的神经元的核的表达和脑源性神经营养因子。为了验证负责AAL的抗AD的动作的分子机制,我们进行了抗体芯片分析,发现表皮生长因子受体/ G蛋白偶联受体激酶2信令在神经元细胞和AD样小鼠模型被激活。此外,使用高效液相色谱法的六个标准化合物的定量分析表明,芦丁是AAL的最丰富的化合物。此外,六个标准化合物功效分析表明,芦丁和异槲皮苷对Aβ聚集显著抑制活性。具有生物活性和化合物的含量合在一起,也许芦丁AAL的生物活性化合物在AD发病。总的来说,我们的发现提供了AAL的AD和AD相关疾病的治疗效果第一的科技支撑。

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