A Social Stimulation Paradigm to Ameliorate Memory Deficit in Alzheimer's Disease.

IF 1 Q3 BIOLOGY
Qiaoyun Ren, Susu Wang, Wei Xie, An Liu
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Abstract

Alzheimer's disease (AD) poses a global health threat, progressively robbing patients of their memory and cognitive abilities. While it is recognized that meaningful social contact can alleviate the symptoms of dementia in AD patients, the precise mechanisms by which social stimulation mitigates AD symptoms remain poorly understood. We found that social interaction with novel mice, also known as novel social, simulated meaningful socializing. Therefore, we developed the multiple novel social (MNS) stimulation paradigm to train AD model mice and found that MNS effectively alleviated cognitive deficits in AD mice. This discovery not only opens up a new avenue for investigating the relationship between social stimulation and Alzheimer's disease but also lays the groundwork for delving into the underlying mechanisms, thereby providing crucial theoretical support for developing novel strategies to treat Alzheimer's disease. Key features • Designing a new social stimulation method to simulate meaningful social interactions in daily life. • The MNS stimulation protocol spans 14 days, with one novel mouse introduced to the subject mice each day. • The subjects were 2.5-month-old FAD4T mice, simulating patients with mild cognitive impairment (MCI). • Results of behavioral tests confirm the efficacy of MNS in reducing cognitive deficits in the AD model. This protocol is used in: J Neurosci (2024), DOI: 10.1523/JNEUROSCI.1689-23.2024.

改善阿尔茨海默病记忆缺陷的社交刺激范式
阿尔茨海默病(AD)对全球健康构成威胁,患者的记忆力和认知能力会逐渐丧失。尽管人们认识到有意义的社交接触可以减轻阿尔茨海默病患者的痴呆症状,但社交刺激减轻阿尔茨海默病症状的确切机制仍然鲜为人知。我们发现,与新奇小鼠的社交互动(也称为新奇社交)可以模拟有意义的社交。因此,我们开发了多重新颖社交(MNS)刺激范式来训练AD模型小鼠,并发现MNS能有效缓解AD小鼠的认知缺陷。这一发现不仅为研究社交刺激与阿尔茨海默病之间的关系开辟了一条新途径,而且为深入研究其潜在机制奠定了基础,从而为开发治疗阿尔茨海默病的新策略提供了重要的理论支持。主要特点 - 设计一种新的社交刺激方法,模拟日常生活中有意义的社交互动。- MNS刺激方案为期14天,每天向受试小鼠介绍一种新的小鼠。- 受试者为2.5个月大的FAD4T小鼠,模拟轻度认知障碍(MCI)患者。- 行为测试结果证实了 MNS 在减少注意力缺失症模型认知障碍方面的疗效。该方案用于J Neurosci (2024),DOI: 10.1523/JNEUROSCI.1689-23.2024。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.50
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