Caloric restriction and intermittent fasting: Two potential diets for successful brain aging

被引:274
作者
Martin, Bronwen
Mattson, Mark P.
Maudsley, Stuart
机构
[1] NIA, Neurosci Lab, Intramural Res Program, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[3] Harbor Hosp, Medstar Res Inst, Baltimore, MD 21225 USA
关键词
caloric restriction; intermittent fasting; aging;
D O I
10.1016/j.arr.2006.04.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The vulnerability of the nervous system to advancing age is all too often manifest in neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. In this review article we describe evidence suggesting that two dietary interventions, caloric restriction (CR) and intermittent fasting (IF), can prolong the health-span of the nervous system by impinging upon fundamental metabolic and cellular signaling pathways that regulate life-span. CR and IF affect energy and oxygen radical metabolism, and cellular stress response systems, in ways that protect neurons against genetic and environmental factors to which they would otherwise succumb during aging. There are multiple interactive pathways and molecular mechanisms by which CR and IF benefit neurons including those involving insulin-like signaling, FoxO transcription factors, sirtuins and peroxisome proliferator-activated receptors. These pathways stimulate the production of protein chaperones, neurotrophic factors and antioxidant enzymes, all of which help cells cope with stress and resist disease. A better understanding of the impact of CR and IF on the aging nervous system will likely lead to novel approaches for preventing and treating neurodegenerative disorders. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:332 / 353
页数:22
相关论文
共 155 条
[71]   Forkhead transcription factor FOXO3a protects quiescent cells from oxidative stress [J].
Kops, GJPL ;
Dansen, TB ;
Polderman, PE ;
Saarloos, I ;
Wirtz, KWA ;
Coffer, PJ ;
Huang, TT ;
Bos, JL ;
Medema, RH ;
Burgering, BMT .
NATURE, 2002, 419 (6904) :316-321
[72]   The PGC-1-related protein PERC is a selective coactivator of estrogen receptor α [J].
Kressler, D ;
Schreiber, SN ;
Knutti, D ;
Kralli, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) :13918-13925
[73]   Peroxisome proliferator-activated receptor α controls the hepatic CYP4A induction adaptive response to starvation and diabetes [J].
Kroetz, DL ;
Yook, P ;
Costet, P ;
Bianchi, P ;
Pineau, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (47) :31581-31589
[74]   The silencing protein SIR2 and its homologs are MAD-dependent protein deacetylases [J].
Landry, J ;
Sutton, A ;
Tafrov, ST ;
Heller, RC ;
Stebbins, J ;
Pillus, L ;
Sternglanz, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5807-5811
[75]   DIET RESTRICTION IN RHESUS-MONKEYS LOWERS FASTING AND GLUCOSE-STIMULATED GLUCOREGULATORY END-POINTS [J].
LANE, MA ;
BALL, SS ;
INGRAM, DK ;
CUTLER, RG ;
ENGEL, J ;
READ, V ;
ROTH, GS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 268 (05) :E941-E948
[76]   Calorie restriction lowers body temperature in rhesus monkeys, consistent with a postulated anti-aging mechanism in rodents [J].
Lane, MA ;
Baer, DJ ;
Rumpler, WV ;
Weindruch, R ;
Ingram, DK ;
Tilmont, EM ;
Cutler, RG ;
Roth, GS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4159-4164
[77]   Gene-expression profile of the ageing brain in mice [J].
Lee, CK ;
Weindruch, R ;
Prolla, TA .
NATURE GENETICS, 2000, 25 (03) :294-297
[78]   Dietary restriction selectively decreases glucocorticoid receptor expression in the hippocampus and cerebral cortex of rats [J].
Lee, J ;
Herman, JP ;
Mattson, MP .
EXPERIMENTAL NEUROLOGY, 2000, 166 (02) :435-441
[79]  
Lee J, 1999, J NEUROSCI RES, V57, P48, DOI 10.1002/(SICI)1097-4547(19990701)57:1<48::AID-JNR6>3.0.CO
[80]  
2-L