首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Qingxin Kaiqiao Recipe Improves Cognitive Performance, Inhibits Apoptosis, and Reduces Pathological Deposits in APP/PS1 Double Transgenic Mice via the PI3K/Akt Pathway
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Qingxin Kaiqiao Recipe Improves Cognitive Performance, Inhibits Apoptosis, and Reduces Pathological Deposits in APP/PS1 Double Transgenic Mice via the PI3K/Akt Pathway

机译:清新猕猴桃配方提高了认知性能,抑制细胞凋亡,并通过PI3K / AKT路径减少了APP / PS1双转基因小鼠的病理沉积物

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The traditional Chinese medicine of Qingxin Kaiqiao Recipe (QKR) is effective in the treatment of Alzheimer’s disease (AD). This study aims to investigate whether QKR improves the cognitive ability and takes neuroprotective effect on APP/PS1 double transgenic mice via the PI3K/Akt pathway. APP/PS1 double transgenic mice were randomly divided into a model, donepezil-treated, or QKR-treated group (L-QKR: 4.75?mg/kg/d, M-QKR: 9.5?mg/kg/d, and H-QKR: 19?mg/kg/d, respectively). Wild-type C57/BL6J mice were used as the control group. Morris water maze (MWM) was used to test the ability of spatial navigation and memorization; terminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL) assay was applied to test the apoptosis; amyloid protein granule deposition was detected via Methenamine silver staining; Western blot (WB) analysis, immunohistochemistry, and RT-PCR were applied to measure the expression of Aβ and corresponding indicators of the PI3K/Akt pathway. Compared with the model group, QKR significantly relieved the cognitive impairment, reduced the deposition of senile plaques, decreased the expression of GSK-3α and Aβ, and increased the expression of p-PI3K, p-Akt, and IDE. In addition, the number of TUNEL-positive cells decreased after treatment using QKR. The current study proved that QKR, especially at the high dose tested, exerted a protective effect on improving learning and memory, inhibiting apoptosis, and reducing the process of pathological degeneration in the hippocampus of AD mice.
机译:清辛凯桥食谱(QKR)中药治疗阿尔茨海默病(AD)是有效的。本研究旨在调查QKR是否改善了认知能力,并通过PI3K / AKT途径对APP / PS1双转基因小鼠进行神经保护作用。将APP / PS1双转基因小鼠随机分为模型,多奈哌齐治疗或QKR处理组(L-QKR:4.75?Mg / Kg / D,M-QKR:9.5?Mg / Kg / D和H- QKR:19?mg / kg / d)。使用野生型C57 / BL6J小鼠作为对照组。莫里斯水迷宫(MWM)用于测试空间导航和记忆的能力;末端脱氧核苷酸转移酶介导的DUTP缺口末端标记(TUNEL)测定用于测试细胞凋亡;通过甲胺银染色检测淀粉样蛋白颗粒沉积;施用免疫印迹(WB)分析,免疫组织化学和RT-PCR测量PI3K / AKT途径的Aβ和相应指标的表达。与模型组相比,QKR显着缓解了认知障碍,减少了老年斑块的沉积,降低了GSK-3α和Aβ的表达,增加了P-PI3K,P-AKT和IDE的表达。此外,使用QKR处理后,在治疗后的子弹阳性细胞的数量减少。目前的研究证明,QKR,尤其是在测试的高剂量,对改善学习和记忆,抑制细胞凋亡以及降低广告小鼠海马病理变性的过程的保护作用。

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