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首页> 外文期刊>CNS neuroscience & therapeutics. >Anthoxanthin Polyphenols Attenuate Aβ Oligomer‐induced Neuronal Responses Associated with Alzheimer's Disease
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Anthoxanthin Polyphenols Attenuate Aβ Oligomer‐induced Neuronal Responses Associated with Alzheimer's Disease

机译:花青素多酚可减轻Aβ寡聚物诱导的与阿尔茨海默氏病相关的神经元反应

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Summary AimsEpidemiological evidence implicates polyphenols as potential natural therapeutics for Alzheimer's disease (AD). To investigate this prospect, five anthoxanthin polyphenols were characterized for their ability to reduce amyloid- β (A β ) oligomer-induced neuronal responses by two mechanisms of action, modulation of oligomerization and antioxidant activity, as well as the synergy between these two mechanisms. MethodsAnthoxanthin oligomerization modulation and antioxidant capabilities were evaluated and correlated with anthoxanthin attenuation of oligomer-induced intracellular reactive oxygen species (ROS) and caspase activation using human neuroblastoma cell treatments designed to isolate these mechanisms of action and to achieve dual-action. ResultsWhile modulation of oligomerization resulted in only minor reductions to neuronal responses, anthoxanthin antioxidant action significantly attenuated oligomer-induced intracellular ROS and caspase activation. Kaempferol uniquely exhibited synergism when the two mechanisms functioned in concert, leading to a pronounced reduction in both ROS and caspase activation. ConclusionsTogether, these findings identify the dominant mechanism by which these anthoxanthins attenuate A β oligomer-induced neuronal responses, elucidate their prospective synergy, and demonstrate the potential of anthoxanthin polyphenols as natural AD therapeutics.
机译:概述流行病学证据表明多酚是阿尔茨海默氏病(AD)的潜在天然疗法。为了研究这一前景,对五种蒽黄嘌呤多酚通过两种作用机制(调节寡聚作用和抗氧化活性)以及两种机制之间的协同作用,降低了淀粉样蛋白-β(Aβ)寡聚物诱导的神经元反应的能力进行了表征。方法使用人类神经母细胞瘤细胞治疗方法来评估蒽醌的低聚调节和抗氧化能力,并将其与寡聚核苷酸诱导的寡聚诱导的细胞内活性氧(ROS)和caspase活化相关,以分离这些作用机制并实现双重作用。结果虽然低聚化的调节仅导致神经元反应的轻微降低,但花青素的抗氧化作用显着减弱了低聚体诱导的细胞内ROS和caspase活化。当两种机制共同起作用时,山竹酚具有独特的协同作用,从而导致ROS和caspase激活均明显降低。结论这些发现共同确定了这些蒽黄素减弱Aβ寡聚体诱导的神经元反应,阐明其前瞻性协同作用的主要机制,并证明了蒽黄嘌呤多酚作为天然AD治疗剂的潜力。

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