Beneficial effects of exercise in a transgenic mouse model of Alzheimer's disease-like Tau pathology

被引:148
作者
Belarbi, Karim [1 ,2 ,3 ]
Burnouf, Sylvie [1 ,2 ,3 ]
Fernandez-Gomez, Francisco-Jose [1 ,2 ]
Laurent, Cyril [1 ,2 ]
Lestavel, Sophie [1 ,4 ,5 ]
Figeac, Martin [1 ]
Sultan, Audrey [1 ,2 ]
Troquier, Laetitia [1 ,2 ]
Leboucher, Antoine [1 ,2 ]
Caillierez, Raphaeelle [1 ,2 ]
Grosjean, Marie-Eve [1 ,2 ]
Demeyer, Dominique [1 ,2 ]
Obriot, Helene [1 ,2 ]
Brion, Ingrid [1 ]
Barbot, Berangere [1 ,2 ]
Galas, Marie-Christine [1 ,2 ]
Staels, Bart [1 ,4 ,5 ]
Humez, Sandrine [1 ,2 ]
Sergeant, Nicolas [1 ,2 ,3 ]
Schraen-Maschke, Susanna [1 ,2 ,3 ]
Muhr-Tailleux, Anne [1 ,4 ,5 ]
Hamdane, Malika [1 ,2 ]
Buee, Luc [1 ,2 ,3 ]
Blum, David [1 ,2 ,3 ]
机构
[1] Univ Lille Nord France, UDSL, F-59000 Lille, France
[2] INSERM, U837, Jean Pierre Aubert Res Ctr, F-59000 Lille, France
[3] CHRU, F-59000 Lille, France
[4] INSERM, U1011, F-59000 Lille, France
[5] Inst Pasteur, F-59000 Lille, France
关键词
Alzheimer's disease; Exercise; Tauopathies; THY-Tau22; Transgenic model; NPC1; PHYSICAL-ACTIVITY; SYNAPTIC PLASTICITY; NEUROTROPHIC FACTOR; GROWTH-FACTOR; NEUROFIBRILLARY TANGLES; MICROGLIAL ACTIVATION; COGNITIVE PERFORMANCE; MEMORY DEFICITS; SPATIAL MEMORY; BRAIN;
D O I
10.1016/j.nbd.2011.04.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tau pathology is encountered in many neurodegenerative disorders known as tauopathies, including Alzheimer's disease. Physical activity is a lifestyle factor affecting processes crucial for memory and synaptic plasticity. Whether long-term voluntary exercise has an impact on Tau pathology and its pathophysiological consequences is currently unknown. To address this question, we investigated the effects of long-term voluntary exercise in the THY-Tau22 transgenic model of Alzheimer's disease-like Tau pathology, characterized by the progressive development of Tau pathology, cholinergic alterations and subsequent memory impairments. Three-month-old THY-Tau22 mice and wild-type littermates were assigned to standard housing or housing supplemented with a running wheel. After 9 months of exercise, mice were evaluated for memory performance and examined for hippocampal Tau pathology, cholinergic defects, inflammation and genes related to cholesterol metabolism. Exercise prevented memory alterations in THY-Tau22 mice. This was accompanied by a decrease in hippocampal Tau pathology and a prevention of the loss of expression of choline acetyltransferase within the medial septum. Whereas the expression of most cholesterol-related genes remained unchanged in the hippocampus of running THY-Tau22 mice, we observed a significant upregulation in mRNA levels of NPC1 and NPC2, genes involved in cholesterol trafficking from the lysosomes. Our data support the view that long-term voluntary physical exercise is an effective strategy capable of mitigating Tau pathology and its pathophysiological consequences. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:486 / 494
页数:9
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