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Methods Mol Biol. 2018;1727:343-352. doi: 10.1007/978-1-4939-7571-6_25.
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Transl Psychiatry. 2017 Dec 8;7(12):1267. doi: 10.1038/s41398-017-0013-6.
3
Environmental enrichment improves hippocampal function in aged rats by enhancing learning and memory, LTP, and mGluR5-Homer1c activity.环境丰容通过增强学习和记忆、LTP 和 mGluR5-Homer1c 活性来改善老年大鼠的海马功能。
Neurobiol Aging. 2018 Mar;63:1-11. doi: 10.1016/j.neurobiolaging.2017.11.004. Epub 2017 Nov 16.
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Absence of microglial CX3CR1 impairs the synaptic integration of adult-born hippocampal granule neurons.小胶质细胞 CX3CR1 的缺失会损害成年海马颗粒神经元的突触整合。
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Behav Processes. 2017 Nov;144:66-71. doi: 10.1016/j.beproc.2017.09.009. Epub 2017 Sep 14.
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锻炼新生神经元以战胜阿尔茨海默病。

Exercising New Neurons to Vanquish Alzheimer Disease.

作者信息

Llorens-Martín María

机构信息

Department of Molecular Neuropathology, Centro de Biología Molecular "Severo Ochoa", CBMSO, CSIC-UAM, Madrid, Spain.

Center for Networked Biomedical Research on Neurodegenerative Diseases CIBERNED, Madrid, Spain.

出版信息

Brain Plast. 2018 Dec 12;4(1):111-126. doi: 10.3233/BPL-180065.

DOI:10.3233/BPL-180065
PMID:30564550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6296267/
Abstract

Alzheimer disease (AD) is the most common type of dementia in individuals over 65 years of age. The neuropathological hallmarks of the condition are Tau neurofibrillary tangles and Amyloid-β senile plaques. Moreover, certain susceptible regions of the brain experience a generalized lack of neural plasticity and marked synaptic alterations during the progression of this as yet incurable disease. One of these regions, the hippocampus, is characterized by the continuous addition of new neurons throughout life. This phenomenon, named adult hippocampal neurogenesis (AHN), provides a potentially endless source of new synaptic elements that increase the complexity and plasticity of the hippocampal circuitry. Numerous lines of evidence show that physical activity and environmental enrichment (EE) are among the most potent positive regulators of AHN. Given that neural plasticity is markedly decreased in many neurodegenerative diseases, the therapeutic potential of making certain lifestyle changes, such as increasing physical activity, is being recognised in several non-pharmacologic strategies seeking to slow down or prevent the progression of these diseases. This review article summarizes current evidence supporting the putative therapeutic potential of EE and physical exercise to increase AHN and hippocampal plasticity both under physiological and pathological circumstances, with a special emphasis on neurodegenerative diseases and AD.

摘要

阿尔茨海默病(AD)是65岁以上人群中最常见的痴呆类型。该病的神经病理学特征是 Tau 神经原纤维缠结和淀粉样β老年斑。此外,在这种目前仍无法治愈的疾病进展过程中,大脑的某些易感区域会出现普遍的神经可塑性缺乏和明显的突触改变。其中一个区域是海马体,其特征是在一生中不断有新神经元生成。这种现象被称为成年海马体神经发生(AHN),它提供了一个潜在的无穷无尽的新突触元件来源,增加了海马体回路的复杂性和可塑性。大量证据表明,体育活动和环境富集(EE)是AHN最有力的正向调节因素。鉴于在许多神经退行性疾病中神经可塑性明显降低,在一些试图减缓或预防这些疾病进展的非药物策略中,改变某些生活方式(如增加体育活动)的治疗潜力正得到认可。这篇综述文章总结了当前的证据,支持EE和体育锻炼在生理和病理情况下增加AHN和海马体可塑性的假定治疗潜力,特别强调了神经退行性疾病和AD。