SIRT1 and neuronal diseases

被引:93
作者
Tang, Bor Luen [1 ]
Chua, Christelle En Lin [1 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
关键词
Alzheimer's disease; Huntington's disease; neurodegeneration; neuron; SIRT1; sirtuin;
D O I
10.1016/j.mam.2007.02.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SIRT1 is the mammalian homologue of yeast silent information regulator (Sir)-2, a member of the sirtuin family of protein deacetylases which have gained much attention as mediators of lifespan extension in several model organisms. Induction of SIRT1 expression also attenuates neuronal degeneration and death in animal models of Alzheimer's disease and Huntington's disease. SIRT1 induction, either by sirtuin activators such as resveratrol, or metabolic conditioning associated with caloric restriction (CR), could be neuroprotective in several ways. It could promote the non-amyloidogenic cleavage of the amyloid precursor protein, enhance clearance of amyloid P-peptides, and reduced neuronal damage through potential inhibition of neuroinflammatory signaling pathways. In addition, increased SIRT1 activity could alter neuronal transcription profiles to enhance anti-stress and anti-apoptotic gene activities, and has been proposed to underlie the inhibition of axonal degeneration in the Wallerian degeneration slow (Wld(s)) phenotype. As neuronal degeneration is a major pathophysiological aspect of human aging, understanding the mechanism of SIRT1 neuroprotection promises novel strategies in clinical intervention of neurodegenerative diseases. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:187 / 200
页数:14
相关论文
共 126 条
[1]   Silent information regulator 2α, a longevity factor and class III histone deacetylase, is an essential endogenous apoptosis inhibitor in cardiac myocytes [J].
Alcendor, RR ;
Kirshenbaum, LA ;
Imai, S ;
Vatner, SF ;
Sadoshima, J .
CIRCULATION RESEARCH, 2004, 95 (10) :971-980
[2]   Nuclear factor-κB modulates the p53 response in neurons exposed to DNA damage [J].
Aleyasin, H ;
Cregan, SP ;
Iyirhiaro, G ;
O'Hare, MJ ;
Callaghan, SM ;
Slack, RS ;
Park, DS .
JOURNAL OF NEUROSCIENCE, 2004, 24 (12) :2963-2973
[3]   SIRT1: Linking adaptive cellular responses to aging-associated changes in organismal physiology [J].
Anastasiou, Dimitrios ;
Krek, Wilhelm .
PHYSIOLOGY, 2006, 21 :404-410
[4]   Nicotinamide and PNC1 govern lifespan extension by calorie restriction in Saccharomyces cerevisiae [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Sinclair, DA .
NATURE, 2003, 423 (6936) :181-185
[5]   Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels [J].
Anderson, RM ;
Bitterman, KJ ;
Wood, JG ;
Medvedik, O ;
Cohen, H ;
Lin, SS ;
Manchester, JK ;
Gordon, JI ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18881-18890
[6]   Resveratrol - A boon for treating Alzheimer's disease? [J].
Anekonda, Thimmappa S. .
BRAIN RESEARCH REVIEWS, 2006, 52 (02) :316-326
[7]   Neuronal protection by sirtuins in Alzheimer's disease [J].
Anekonda, TS ;
Reddy, PH .
JOURNAL OF NEUROCHEMISTRY, 2006, 96 (02) :305-313
[8]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[9]   Tau phosphorylation and aggregation in Alzheimer's disease pathology [J].
Avila, J .
FEBS LETTERS, 2006, 580 (12) :2922-2927
[10]   Non-steroidal anti-inflammatory drugs stimulate secretion of non-amyloidogenic precursor protein [J].
Avramovich, Y ;
Amit, T ;
Youdim, MBH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (35) :31466-31473