Modulation of glymphatic system by visual circuit activation alleviates memory impairment and apathy in a mouse model of Alzheimer’s disease

冷漠 淋巴系统 神经科学 海马结构 阿尔茨海默病 医学 赫兹 疾病 认知 心理学 病理 物理 脑脊液 量子力学
作者
Wen Wu,Yubai Zhao,Xin R. Cheng,Xuelong Xie,Y. J. Zeng,Tao Quan,Yishuai Yang,Chuan Xiao,Zhan Zhang,Jiahui Pang,Jian Jin,Hongbo He,Yangyang Lin,Boxing Li,Jin‐Feng Ma,Xiaojing Ye,Wei‐Jye Lin
出处
期刊:Nature Communications [Springer Nature]
卷期号:16 (1)
标识
DOI:10.1038/s41467-024-55678-w
摘要

Alzheimer's disease is characterized by progressive amyloid deposition and cognitive decline, yet the pathological mechanisms and treatments remain elusive. Here we report the therapeutic potential of low-intensity 40 hertz blue light exposure in a 5xFAD mouse model of Alzheimer's disease. Our findings reveal that light treatment prevents memory decline in 4-month-old 5xFAD mice and motivation loss in 14-month-old 5xFAD mice, accompanied by restoration of glial water channel aquaporin-4 polarity, improved brain drainage efficiency, and a reduction in hippocampal lipid accumulation. We further demonstrate the beneficial effects of 40 hertz blue light are mediated through the activation of the vLGN/IGL-Re visual circuit. Notably, concomitant use of anti-Aβ antibody with 40 hertz blue light demonstrates improved soluble Aβ clearance and cognitive performance in 5xFAD mice. These findings offer functional evidence on the therapeutic effects of 40 hertz blue light in Aβ-related pathologies and suggest its potential as a supplementary strategy to augment the efficacy of antibody-based therapy. Treatments for Alzheimer's disease (AD) remain limited. Here, the authors show that 40 hertz blue light activates a visual circuit to boost glymphatic drainage, and enhances memory, motivation, and anti-Aβ therapy efficacy in a mouse model of AD.
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