Neuroprotective role of intermittent fasting in senescence-accelerated mice P8 (SAMP8)

被引:35
作者
Tajes, M. [1 ]
Gutierrez-Cuesta, J. [1 ]
Folch, J. [2 ]
Ortuno-Sahagun, D. [3 ]
Verdaguer, E. [1 ]
Jimenez, A. [1 ]
Junyent, F. [2 ]
Lau, A. [4 ]
Camins, A. [1 ]
Pallas, M. [1 ]
机构
[1] Univ Barcelona, Nucli Univ Pedralbes, Unitat Farmacol & Farmacognosia, Fac Farm,Inst Biomed IBUB, E-08028 Barcelona, Spain
[2] Univ Rovira & Virgili, Unitat Bioquim, Fac Med & Ciencies Salut, E-43201 Reus, Tarragona, Spain
[3] Univ Guadalajara, CUCBA, Dept Biol Celular & Mol, Lab Desarrollo & Regenerac Neural,Inst Neurobiol, Guadalajara 44430, Jalisco, Mexico
[4] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
关键词
Ageing; Neurodegeneration; NF kappa B; ADAM10; BDNF; Sirtuin; 1; CALORIC RESTRICTION; ALZHEIMERS-DISEASE; DIETARY RESTRICTION; MOUSE SAM; BRAIN; SIRT1; RISK; EXPRESSION; MODELS; DEACETYLASE;
D O I
10.1016/j.exger.2010.04.010
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
Dietary interventions have been proposed as a way to increase lifespan and improve health. The senescence-accelerated prone 8 (SAMP8) mice have a shorter lifespan and show alterations in the central nervous system. Moreover, this mouse strain shows decreased sirtuin 1 protein expression and elevated expression of the acetylated targets NF kappa B and FoxO1, which are implicated in transcriptional control of key genes in cell proliferation and cell survival, in reference to control strain, SAMR1. After eight weeks of intermittent fasting, sirtuin 1 protein expression was recovered in SAMP8. This recovery was accompanied by a reduction in the two acetylated targets. Furthermore, SAMP8 showed a lower protein expression of BDNF and HSP70 while intermittent fasting re-established normal values. The activation of JNK and FoxO1 was also reduced in SAMP8 mice subjected to an IF regimen, compared with control SAMP8. Our findings provide new insights into the participation of sirtuin 1 in ageing and point to a potential novel application of this enzyme to prevent frailty due to ageing processes in the brain. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:702 / 710
页数:9
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