Quercetin mediated lifespan extension in Caenorhabditis elegans is modulated by age-1, daf-2, sek-1 and unc-43

被引:131
作者
Pietsch, Kerstin [1 ]
Saul, Nadine [1 ]
Menzel, Ralph [1 ]
Stuerzenbaum, Stephen R. [2 ]
Steinberg, Christian E. W. [1 ]
机构
[1] Humboldt Univ, Lab Freshwater & Stress Ecol, Dept Biol, D-12437 Berlin, Germany
[2] Kings Coll London, Div Pharmaceut Sci, Sch Biomed & Hlth Sci, London SE19NH, England
基金
美国国家卫生研究院;
关键词
C; elegans; Quercetin; Lifespan; age-1; daf-2; unc-43; sek-1; OXIDATIVE STRESS; CALORIE RESTRICTION; SIGNAL-TRANSDUCTION; LONGEVITY; POLYPHENOLS; FLAVONOIDS; RESISTANCE; FOOD; THERMOTOLERANCE; ANTIOXIDANTS;
D O I
10.1007/s10522-008-9199-6
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
The nematode Caenorhabditis elegans responds to flavonoid-rich diets with improved health and longevity. The precise mechanism(s) responsible for this remains to be identified, but is believed to be linked to the highly antioxidative properties of flavonoids. This study provides a dissection of lifespan modulation by the flavonoid quercetin. In detail, quercetin was shown not to act as a simple antimicrobial agent or exclusively via radical scavenging capacities. Likewise, lifespan extension had no effect on reproduction and body length. Furthermore, neither a caloric restriction mimetic nor a sirtuin (sir-2.1) dependence was identified as a likely mode of action. However, four genes were pinpointed to be required for the quercetin derived lifespan extension, namely age-1, daf-2, unc-43 and sek-1. The latter two have, to date, not been linked to quercetin-mediated lifespan extension.
引用
收藏
页码:565 / 578
页数:14
相关论文
共 72 条
[1]   SKN-1 links C-elegans mesendodermal specification to a conserved oxidative stress response [J].
An, JH ;
Blackwell, TK .
GENES & DEVELOPMENT, 2003, 17 (15) :1882-1893
[2]   Genetics of aging in Caenorhabditis elegans [J].
Antebi, Adam .
PLOS GENETICS, 2007, 3 (09) :1565-1571
[3]   Endocrine signaling in Caenorhabditis elegans controls stress response and longevity [J].
Baumeister, Ralf ;
Schaffitzel, Elke ;
Hertweck, Maren .
JOURNAL OF ENDOCRINOLOGY, 2006, 190 (02) :191-202
[4]   C. elegans SIR-2.1 interacts with 14-3-3 proteins to activate DAF-16 and extend life span [J].
Berdichevsky, Ala ;
Viswanathan, Mohan ;
Horvitz, H. Robert ;
Guarente, Leonard .
CELL, 2006, 125 (06) :1165-1177
[5]   Genetic links between diet and lifespan: shared mechanisms from yeast to humans [J].
Bishop, Nicholas A. ;
Guarente, Leonard .
NATURE REVIEWS GENETICS, 2007, 8 (11) :835-844
[6]  
BRENNER S, 1974, GENETICS, V77, P71
[7]   Beneficial effects of natural antioxidants EGCG and α-lipoic acid on life span and age-dependent behavioral declines in Caenorhabditis elegans [J].
Brown, Marishka K. ;
Evans, Joseph L. ;
Luo, Yuan .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2006, 85 (03) :620-628
[8]   Oxidative stress enzymes are required for DAF-16-mediated immunity due to generation of reactive oxygen species by Caenorhabditis elegans [J].
Chavez, Violeta ;
Mohri-Shiomi, Akiko ;
Maadani, Arash ;
Vega, Luis Alberto ;
Garsin, Danielle A. .
GENETICS, 2007, 176 (03) :1567-1577
[9]   SIR2: a potential target for calorie restriction mimetics [J].
Chen, Danica ;
Guarente, Leonard .
TRENDS IN MOLECULAR MEDICINE, 2007, 13 (02) :64-71
[10]   Antiinflammatory constituents from Heterotheca inuloides [J].
Delgado, G ;
Olivares, MD ;
Chávez, MI ;
Ramírez-Apan, T ;
Linares, E ;
Bye, R ;
Espinosa-García, FJ .
JOURNAL OF NATURAL PRODUCTS, 2001, 64 (07) :861-864