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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Herbal Extracts Combination (WNK) Prevents Decline in Spatial Learning and Memory in APP/PS1 Mice through Improvement of Hippocampal A beta Plaque Formation, Histopathology, and infrastructure
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Herbal Extracts Combination (WNK) Prevents Decline in Spatial Learning and Memory in APP/PS1 Mice through Improvement of Hippocampal A beta Plaque Formation, Histopathology, and infrastructure

机译:草药提取物组合(WNK)通过改善海马β斑块形成,组织病理学和基础设施,防止在APP / PS1小鼠中的空间学习和记忆下降

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摘要

To investigate the cognitive enhancement effect of WNK, an extracts combination of P. ginseng, G. biloba, and C. sativus L. and possible mechanisms, 5-month-old APP/PS1 transgenic mice were used in this study. After 3 months of administration, all mice received Morris water maze (MWM) training and a probe test. Mouse brain sections were detected by immunohistochemistry, HE staining, and transmission electron microscopy. MWM results showed significant difference between transgenic mice and non-transgenic littermates (P < 0.05, P < 0.01). WNK-treated mice exhibited enhanced maze performance over the training progression, especially better spatial memory retention in probe test compared to transgenic mice (P < 0.05, P < 0.01) and better spatial learning and memory at the fourth day of MWM test compared to EGB761- (G. biloba extract-) treated ones (P < 0.05). Hippocampal A/3 plaque burden significantly differed between APP/PS1 and littermate mice (P < 0.001), while decreased AjS plaque appeared in WNK- or EGB761-treated transgenic brains (P < 0.05). Neurodegenerative changes were evident from light microscopic and ultrastructural observations in transgenic brains, which were improved by WNK or EGB761 treatment. These data indicate WNK can reduce the decline in spatial cognition, which might be due to its effects on reducing A/3 plaque formation and ameliorating histopathology and ultrastructure in hippocampus of APP/PS1 mouse brain.
机译:为了探讨WNK的认知增强效果,本研究中使用了P.人参,G.Biloba和C.Sativus L.以及可能的机制,5个月大的APP / PS1转基因小鼠的提取物组合。在3个月后给药后,所有小鼠都接受了莫里斯水迷宫(MWM)训练和探测试验。通过免疫组织化学,HE染色和透射电子显微镜检测小鼠脑切片。 MWM结果表明转基因小鼠和非转基因凋落物之间的显着差异(P <0.05,P <0.01)。与EGB761相比,WNK处理的小鼠在训练进展上表现出增强的迷宫性能,特别是探针测试中的探针测试中的更好的空间记忆保留(P <0.05,P <0.01),而MWM测试的第四天在MWM测试的第四天进行了更好的空间学习和记忆 - (G. BiLoba提取物 - )处理过的(P <0.05)。海马A / 3斑块负担在APP / PS1和凋落物小鼠之间显着不同(P <0.001),而WNK或EGB761处理的转基因大脑中出现降低的AJS斑块(P <0.05)。从转基因大脑中的光学显微镜和超微结构观察中明显是神经变性的变化,其通过WNK或EGB761治疗得到改善。这些数据表明,WNK可以降低空间认知的下降,这可能是由于其对降低A / 3斑块形成和改善APP / PS1小鼠脑中海马卡的组织病理学和超微结构的影响。

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