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Codonopsis pilosula polysaccharide attenuates Aβ toxicity and cognitive defects in APP/PS1 mice

机译:Codonopsis pilosula多糖衰减APP / PS1小鼠中的Aβ毒性和认知缺陷

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摘要

Polysaccharides (CPPs), a traditional Chinese medicine used for thousands of years, is a potential neuroprotective polysaccharide via a relatively poorly understood mechanism. We previously reported that CPPs attenuated tau pathology in hTau transfected mice and therefore in the current work investigated the effect of CPPs on Aβ toxicity and cognitive defects in APP/PS1 mice model. It was found that one-month intragastric administration of CPPs significantly ameliorated cognitive defects in APP/PS1 mice. In addition, CPPs treatment mitigated the loss of the synaptic plasticity and increased the synaptic proteins including synaptotagmin and PSD95. The expression of Aβ42 and Aβ40 was remarkably decreased in the hippocampus of APP/PS1 mice after CPPs treatment. We also found that CPPs coincubation significantly reduced the amount of APPβ and Aβ42 expression in cells. Intriguingly, the activity of BACE1 was decreased following CPPs treatment in both the hippocampus of APP/PS1 mice and in vitro experiments. Collectively, these results indicated that CPPs attenuated Aβ pathology in APP/PS1 mice, and down-regulating BACE1 might be the underlaying mechanism which could be a therapeutic target for alleviating cognitive defects in AD pathology.
机译:多糖(CPP)是一种使用千年的中药,是千年来的,是一种潜在的神经保护多糖,通过相对较差的机制。我们此前报道,CPP减弱了HTAU转染老鼠的TAU病理学,因此在目前的工作中调查了CPP对APP / PS1小鼠模型中Aβ毒性和认知缺陷的影响。结果发现,APP / PS1小鼠中的一个月内CPP的胃内胃癌可显着改善认知缺陷。此外,CPPS治疗减少了突触塑性的丧失,增加了突触蛋白,包括Synaptotagmin和PSD95。在CPP处理后,APP / PS1小鼠的海马在APPOCAMPUS中表达显着降低。我们还发现CPPS同步显着降低了细胞中APPβ和Aβ42表达的量。有趣的是,在APP / PS1小鼠的海马和体外实验中,CPP治疗后,BACE1的活性降低。总的来说,这些结果表明,CPP减弱了APP / PS1小鼠中的Aβ病理学,下调BACE1可能是用于减轻广告病理中的认知缺陷的治疗靶标的底层机制。

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