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揭示低密度脂蛋白受体相关蛋白1(LRP1)在阿尔茨海默病中的作用:聚焦于β-淀粉样蛋白清除及肝脑轴

Unraveling the Role of LRP1 in Alzheimer's Disease: A Focus on Aβ Clearance and the Liver-Brain Axis.

作者信息

Yang Wanyue, Wei Zilin, Wang Tianhui

机构信息

Tianjin Key Laboratory of Exercise Physiology & Sports Medicine, Tianjin University of Sport, Tianjin, 301617, China.

Military Medical Sciences Academy, 1 Dali Road, Heping District, Tianjin, 300050, P.R. China.

出版信息

J Mol Neurosci. 2025 Apr 1;75(2):43. doi: 10.1007/s12031-025-02339-2.

Abstract

Alzheimer's disease (AD) is the most prevalent form of dementia, significantly contributing to the global health burden. The progressive accumulation of amyloid-beta (Aβ) plaques and tau tangles triggers neuroinflammation, oxidative stress, and neuronal damage, highlighting the critical need for effective clearance mechanisms. Recent research has identified low-density lipoprotein receptor-related protein 1 (LRP1) as a key factor in the regulation of Aβ clearance, neuroinflammation, and blood-brain barrier integrity, particularly in relation to the liver-brain axis. This review provides a comprehensive examination of the role of LRP1 in AD, focusing on its expression in the brain and liver, its contribution to Aβ metabolism, and its potential as a therapeutic target. Using a systematic literature review, LRP1's multifaceted roles across various biological processes were explored, including its involvement in Aβ transport, clearance via the liver, and modulation of neuroinflammation. Additionally, the impact of physical exercise, pharmacological interventions, and dietary factors on LRP1 expression levels was investigated, elucidating how these approaches may enhance Aβ clearance. The findings demonstrate that LRP1 expression decreases progressively as AD advances, and that augmenting LRP1 activity-particularly through exercise and drug therapies-can improve Aβ clearance and reduce neuroinflammatory responses. Furthermore, LRP1's involvement in the liver-brain axis reveals its broader systemic role in AD pathology. In conclusion, targeting LRP1 offers a promising avenue for AD prevention and treatment, providing new insights into the therapeutic potential of enhancing Aβ clearance pathways through the liver-brain axis.

摘要

阿尔茨海默病(AD)是最常见的痴呆形式,对全球健康负担有重大影响。淀粉样β(Aβ)斑块和tau缠结的进行性积累引发神经炎症、氧化应激和神经元损伤,凸显了有效清除机制的迫切需求。最近的研究已确定低密度脂蛋白受体相关蛋白1(LRP1)是调节Aβ清除、神经炎症和血脑屏障完整性的关键因素,特别是在肝脑轴方面。本综述全面考察了LRP1在AD中的作用,重点关注其在脑和肝脏中的表达、对Aβ代谢的贡献及其作为治疗靶点的潜力。通过系统的文献综述,探讨了LRP1在各种生物过程中的多方面作用,包括其参与Aβ转运、通过肝脏清除以及对神经炎症的调节。此外,还研究了体育锻炼、药物干预和饮食因素对LRP1表达水平的影响,阐明了这些方法如何增强Aβ清除。研究结果表明,随着AD的进展,LRP1表达逐渐降低,增强LRP1活性——特别是通过运动和药物治疗——可以改善Aβ清除并减少神经炎症反应。此外,LRP1在肝脑轴中的作用揭示了其在AD病理中的更广泛的全身作用。总之,以LRP1为靶点为AD的预防和治疗提供了一条有前景的途径,为通过肝脑轴增强Aβ清除途径的治疗潜力提供了新的见解。

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