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Yizhiqingxin Formula Alleviates Cognitive Deficits and Enhances Autophagy via mTOR Signaling Pathway Modulation in Early Onset Alzheimer’s Disease Mice

机译:益智清心方通过阿尔茨海默氏病早期发病小鼠的mTOR信号通路调节减轻认知缺陷并增强自噬。

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摘要

Alzheimer’s disease (AD) is the most common type of dementia worldwide. The deposition of amyloid β (Aβ) is one of the most important pathological changes in AD. Autophagy, which mediates degradation of toxic proteins and maintains normal neuronal function, is dysfunctional in AD; dysfunctional autophagy is believed to be a critical pathological feature of AD. Here, we evaluated the in vitro and in vivo effects of a traditional Chinese medicinal formula called Yizhiqingxin formula (YQF) on autophagy. We determined that treatment with a high dose of YQF improved spatial memory and decreased the hippocampal Aβ burden in APP/PS1 mice, an early onset AD model. Transmission electron microscopy and immunohistochemical data revealed that YQF enhanced autophagosome formation and also increased the levels of LC3II/LC3I and Beclin1. Further, we found that YQF treatment promoted autophagic activity by inhibiting the phosphorylation of the Mammalian target of rapamycin (mTOR) at the Ser2448 site. Moreover, the level of 4EBP1 increased after YQF intervention, indicating a suppression of mTOR signaling. YQF was also found to promote autophagosome degradation, as indicated by the decreased p62 levels and increased cathepsin D and V-ATPase levels. Taken together, YQF could improve spatial learning in APP/PS1 mice and ameliorate the accumulation of Aβ while promoting autophagy via mTOR pathway modulation.
机译:阿尔茨海默氏病(AD)是全世界最常见的痴呆类型。淀粉样蛋白β(Aβ)的沉积是AD最重要的病理变化之一。自噬介导毒性蛋白质的降解并维持正常的神经元功能,在AD中功能失调。自噬功能障碍被认为是AD的关键病理特征。在这里,我们评估了称为益智清心配方(YQF)的中药对自噬的体外和体内作用。我们确定在早期发病的AD模型APP / PS1小鼠中,高剂量的YQF治疗可改善空间记忆并降低海马Aβ负担。透射电镜和免疫组织化学数据表明,YQF增强了自噬体的形成,还增加了LC3II / LC3I和Beclin1的水平。此外,我们发现YQF处理通过抑制Ser2448位点的雷帕霉素哺乳动物靶标(mTOR)的磷酸化来促进自噬活性。此外,YQF干预后4EBP1的水平增加,表明抑制了mTOR信号传导。还发现YQF可以促进自噬体降解,如p62水平降低以及组织蛋白酶D和V-ATPase水平升高所表明。综上所述,YQF可以改善APP / PS1小鼠的空间学习,改善Aβ的积累,同时通过mTOR途径调节促进自噬。

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