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[提取物名称]的水提取物通过抑制乙酰胆碱酯酶活性和乙酰胆碱信号通路来改善与年龄相关的认知衰退。

Water extract of improves age‑related cognitive decline by inhibiting acetylcholinesterase activity and the acetylcholine signaling pathway.

作者信息

Kim Ju-Eun, Min Kyeong-Seon, Go Jun, Park Hye-Yeon, Choi Young-Keun, Lee In-Bok, Shin Jaewon, Cho Hyun-Ju, Kim Hong-Sik, Hwang Dae Youn, Oh Won-Keun, Kim Kyoung-Shim, Lee Chul-Ho

机构信息

Laboratory Animal Resource Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Republic of Korea.

Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

Mol Med Rep. 2025 May;31(5). doi: 10.3892/mmr.2025.13496. Epub 2025 Mar 21.

DOI:10.3892/mmr.2025.13496
PMID:40116124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11938412/
Abstract

The aging process is associated with a decline in certain cognitive abilities, including learning and memory. This age‑related cognitive decline is associated with a reduction in neurogenesis and alterations in the cholinergic system. (HJ), an ornamental plant in the family , has been reported to exert beneficial effects against neurodegenerative pathophysiologies in mouse models of disorders such as Alzheimer's and Parkinson's disease. Despite the increasingly aging populations of numerous societies, no study has yet investigated the effects of HJ on cognitive decline associated with normal aging. The present study therefore aimed to examine the protective potential of HJ water (HJW) extract against age‑related cognitive decline and scopolamine‑induced cognitive impairment. The analyses revealed that the oral administration of HJW markedly improved novel objective recognition and spatial learning in the novel object recognition and Morris water maze tests, respectively, in aged mice. The administration of 600 mg/kg HJW further increased neurogenesis and CA1 thickness in the hippocampi of aged mice. In scopolamine‑induced cognitive impairment, administration of 400 or 600 mg/kg HJW markedly increased novel object recognition performance in scopolamine‑treated mice. The inhibitory effect of HJW on acetylcholinesterase (AChE) and the activation effects of HJW on the calcium/calmodulin‑dependent kinase (CaMK)IIα‑cAMP response element‑binding protein (CREB) and AKT‑glycogen synthase kinase‑3 β (GSK3β) pathways were further demonstrated. Overall, these results indicate that HJW administration improves cognitive function through the regulation of AChE activity and CaMKIIα‑CREB and AKT‑GSK3β pathways.

摘要

衰老过程与某些认知能力的下降有关,包括学习和记忆。这种与年龄相关的认知下降与神经发生减少和胆碱能系统改变有关。(HJ)是一种属于……科的观赏植物,据报道在阿尔茨海默病和帕金森病等疾病的小鼠模型中,对神经退行性病理生理具有有益作用。尽管众多社会的人口老龄化日益严重,但尚无研究调查HJ对与正常衰老相关的认知下降的影响。因此,本研究旨在检验HJ水提取物(HJW)对与年龄相关的认知下降和东莨菪碱诱导的认知障碍的保护潜力。分析表明,口服HJW分别显著改善了老年小鼠在新物体识别和莫里斯水迷宫测试中的新物体识别和空间学习能力。给予600mg/kg的HJW进一步增加了老年小鼠海马体中的神经发生和CA1厚度。在东莨菪碱诱导的认知障碍中,给予400或600mg/kg的HJW显著提高了东莨菪碱处理小鼠的新物体识别性能。进一步证明了HJW对乙酰胆碱酯酶(AChE)的抑制作用以及对钙/钙调蛋白依赖性激酶(CaMK)IIα-环磷酸腺苷反应元件结合蛋白(CREB)和AKT-糖原合酶激酶-3β(GSK3β)通路的激活作用。总体而言,这些结果表明,给予HJW通过调节AChE活性以及CaMKIIα-CREB和AKT-GSK3β通路来改善认知功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/9256dfeac086/mmr-31-05-13496-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/9897e3c34766/mmr-31-05-13496-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/04b1aa7724cc/mmr-31-05-13496-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/72ca3aa70aa7/mmr-31-05-13496-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/4dedd400ceaa/mmr-31-05-13496-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/c84110e4604d/mmr-31-05-13496-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/f22009d96a26/mmr-31-05-13496-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/cfb327ed7802/mmr-31-05-13496-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/9256dfeac086/mmr-31-05-13496-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/9897e3c34766/mmr-31-05-13496-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/04b1aa7724cc/mmr-31-05-13496-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/72ca3aa70aa7/mmr-31-05-13496-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/4dedd400ceaa/mmr-31-05-13496-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/c84110e4604d/mmr-31-05-13496-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/f22009d96a26/mmr-31-05-13496-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/cfb327ed7802/mmr-31-05-13496-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/11938412/9256dfeac086/mmr-31-05-13496-g07.jpg

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