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四羟基二苯乙烯葡萄糖苷可改善 APP/PS1 转基因小鼠的认知功能障碍和病理变化。

Tetrahydroxy Stilbene Glucoside Ameliorates Cognitive Impairments and Pathology in APP/PS1 Transgenic Mice.

机构信息

Department of Pharmacy, Xuanwu Hospital of Capital Medical University, Beijing, 100053, China.

Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing, 100053, China.

出版信息

Curr Med Sci. 2021 Apr;41(2):279-286. doi: 10.1007/s11596-021-2344-z. Epub 2021 Apr 20.

DOI:10.1007/s11596-021-2344-z
PMID:33877543
Abstract

Cognitive impairment is the main clinical manifestation of Alzheimer's disease (AD), and amyloid-β (Aβ) deposition and senile plaques are the characteristic neuropathological hallmarks in AD brains. This study aimed to explore the effect and mechanism of tetrahydroxy stilbene glucoside (TSG) on cognitive function in APP/PS1 mice during long-term administration. Here, we treated APP/PS1 model mice of AD with different doses of TSG (50 mg/kg and 100 mg/kg) for 5 to 17 months by gavage, and we further observed whether TSG could ameliorate the cognitive decline in APP/PS1 mice using behavioral tests, and investigated the possible mechanisms by immunohistochemistry and Western blotting. Our results showed that TSG treatment rescued the spatial and non-spatial learning and memory impairments of APP/PS1 mice at Morris water maze test and novel object recognition test. Furthermore, Aβ40/42 deposition in the cortex and hippocampus of APP/PS1 mice treated with TSG was significantly reduced compared to the wild type mice using the immunohistochemical technique. Finally, Western blotting showed that TSG primarily decreased the APP expression to avoid the Aβ plaque deposition in the cortex and hippocampus of mice. These results reveal the beneficial effects of TSG in APP/PS1-AD mice, which may be associated with the reduction of Aβ deposits in the brain.

摘要

认知障碍是阿尔茨海默病(AD)的主要临床症状,淀粉样蛋白-β(Aβ)沉积和老年斑是 AD 大脑的特征性神经病理学标志。本研究旨在探讨长期给予四羟基二苯乙烯葡萄糖苷(TSG)对 APP/PS1 小鼠认知功能的影响及其机制。在这里,我们通过灌胃用不同剂量的 TSG(50mg/kg 和 100mg/kg)处理 AD 模型 APP/PS1 小鼠 5 至 17 个月,并进一步通过行为测试观察 TSG 是否能改善 APP/PS1 小鼠的认知功能下降,通过免疫组织化学和 Western blot 分析研究可能的机制。我们的结果表明,TSG 处理可挽救 APP/PS1 小鼠在 Morris 水迷宫测试和新物体识别测试中的空间和非空间学习记忆障碍。此外,与野生型小鼠相比,用免疫组织化学技术检测到 TSG 处理的 APP/PS1 小鼠皮质和海马中的 Aβ40/42 沉积明显减少。最后,Western blot 显示 TSG 主要通过降低 APP 的表达来避免 Aβ斑块在小鼠大脑皮质和海马中的沉积。这些结果揭示了 TSG 对 APP/PS1-AD 小鼠的有益作用,这可能与脑内 Aβ 沉积的减少有关。

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