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
相关论文
共 50 条
  • [1] Dysfunction of astrocytes in senescence-accelerated mice SAMP8 reduces their neuroprotective capacity
    Garcia-Matas, Silvia
    Gutierrez-Cuesta, Javier
    Coto-Montes, Ana
    Rubio-Acero, Raquel
    Diez-Vives, Cristina
    Camins, Antoni
    Pallas, Merce
    Sanfeliu, Coral
    Cristofol, Rosa
    AGING CELL, 2008, 7 (05) : 630 - 640
  • [2] Muscle mass, structural and functional investigations of senescence-accelerated mouse P8 (SAMP8)
    Guo, An Yun
    Leung, Kwok Sui
    Siu, Parco Ming Fai
    Qin, Jiang Hui
    Chow, Simon Kwoon Ho
    Qin, Ling
    Li, Chi Yu
    Cheung, Wing Hoi
    EXPERIMENTAL ANIMALS, 2015, 64 (04) : 425 - 433
  • [3] Aβ induces oxidative stress in senescence-accelerated (SAMP8) mice
    Takagane, Kurara
    Nojima, Jun
    Mitsuhashi, Hiroaki
    Suo, Satoshi
    Yanagihara, Dai
    Takaiwa, Fumio
    Urano, Yasuomi
    Noguchi, Noriko
    Ishiura, Shoichi
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2015, 79 (06) : 912 - 918
  • [4] Bioinformatic Analysis Reveals Key Genes and Pathways in Aging Brain of Senescence-accelerated Mouse P8 (SAMP8)
    Li, Jiaqi
    Zhou, Yuzhi
    Du, Guanhua
    Qin, Xuemei
    Gao, Li
    CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2018, 17 (09) : 712 - 722
  • [5] Senescence-accelerated mice prone 8 (SAMP8) in male as a spontaneous osteoarthritis model
    Yohei Sanada
    Yasunari Ikuta
    Chenyang Ding
    Masahiro Shinohara
    Dilimulati Yimiti
    Hiroyuki Ishitobi
    Keita Nagira
    Minjung Lee
    Takayuki Akimoto
    Sachi Shibata
    Masakazu Ishikawa
    Tomoyuki Nakasa
    Kiminori Matsubara
    Martin K. Lotz
    Nobuo Adachi
    Shigeru Miyaki
    Arthritis Research & Therapy, 24
  • [6] Senescence-accelerated mice prone 8 (SAMP8) in male as a spontaneous osteoarthritis model
    Sanada, Yohei
    Ikuta, Yasunari
    Ding, Chenyang
    Shinohara, Masahiro
    Yimiti, Dilimulati
    Ishitobi, Hiroyuki
    Nagira, Keita
    Lee, Minjung
    Akimoto, Takayuki
    Shibata, Sachi
    Ishikawa, Masakazu
    Nakasa, Tomoyuki
    Matsubara, Kiminori
    Lotz, Martin K.
    Adachi, Nobuo
    Miyaki, Shigeru
    ARTHRITIS RESEARCH & THERAPY, 2022, 24 (01)
  • [7] Neuroprotective effects of forsythiaside on learning and memory deficits in senescence-accelerated mouse prone (SAMP8) mice
    Wang, Hong-Mei
    Wang, Li-Wei
    Liu, Xin-Min
    Li, Chang-Lu
    Xu, Shu-Ping
    Farooq, Ahsana-Dar
    PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2013, 105 : 134 - 141
  • [8] Neuroprotective effects of icariin on memory impairment and neurochemical deficits in senescence-accelerated mouse prone 8 (SAMP8) mice
    He, Xiao-Li
    Zhou, Wei-Qin
    Bi, Ming-Gang
    Du, Guan-Hua
    BRAIN RESEARCH, 2010, 1334 : 73 - 83
  • [9] Effects of melatonin in the brain of the senescence-accelerated mice-prone 8 (SAMP8) model
    Gutierrez-Cuesta, Javier
    Tajes, Marta
    Jimenez, Andres
    Camins, Antoni
    Pallas, Merce
    REVISTA DE NEUROLOGIA, 2011, 52 (10) : 618 - 622
  • [10] No effects of lifelong creatine supplementation on sarcopenia in senescence-accelerated mice (SAMP8)
    Derave, W
    Eijnde, BO
    Ramaekers, M
    Hespel, P
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2005, 289 (02): : E272 - E277