Old age potentiates cold-induced tau phosphorylation: linking thermoregulatory deficit with Alzheimer's disease

被引:25
|
作者
Tournissac, Marine [1 ,2 ,3 ]
Vandal, Milene [1 ,2 ,3 ]
Francois, Arnaud [1 ,2 ]
Planel, Emmanuel [2 ,4 ]
Calon, Frederic [1 ,2 ,3 ]
机构
[1] Univ Laval, Fac Pharm, Quebec City, PQ, Canada
[2] CHUL, Ctr Rech, Axe Neurosci, Quebec City, PQ, Canada
[3] Inst Nutr & Aliments Fonct, Quebec City, PQ, Canada
[4] Univ Laval, Fac Med, Dept Psychiat & Neurosci, Quebec City, PQ, Canada
基金
加拿大健康研究院;
关键词
Aging; Thermoregulation; Tau; Alzheimer's disease; Body temperature; BROWN ADIPOSE-TISSUE; COGNITIVE IMPAIRMENT; TEMPERATURE-RANGE; ANIMAL-MODEL; A-BETA; HYPERPHOSPHORYLATION; HYPOTHERMIA; ANESTHESIA; PROTEIN; INHIBITION;
D O I
10.1016/j.neurobiolaging.2016.09.024
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Thermoregulatory deficits coincide with a rise in the incidence of Alzheimer's disease (AD) in old age. Lower body temperature increases tau phosphorylation, a neuropathological hallmark of AD. To determine whether old age potentiates cold-induced tau phosphorylation, we compared the effects of cold exposure (4 degrees C, 24 hours) in 6- and 18-month-old mice. Cold-induced changes in body temperature, brown adipose tissue activity, and phosphorylation of tau at Ser202 were not different between 6- and 18-month-old mice. However, following cold exposure, only old mice displayed a significant rise in soluble tau pThr181 and pThr231, which was correlated with body temperature. Inactivation of glycogen synthase kinase 3 beta was more prominent in young mice, suggesting a protective mechanism against cold-induced tau phosphorylation. These results suggest that old age confers higher susceptibility to tau hyperphosphorylation following a change in body temperature, thereby contributing to an enhanced risk of developing AD. (C) 2016 Elsevier Inc. All rights reserved.
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页码:25 / 29
页数:5
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