Healthy aging - insights from Drosophila

被引:31
作者
Iliadi, Konstantin G. [1 ]
Knight, David [1 ]
Boulianne, Gabrielle L. [1 ,2 ]
机构
[1] Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Drosophila; lifespan; aging; genetics; environment; LONG-LIVED STRAIN; PROBOSCIS-EXTENSION RESPONSE; OXIDATIVE STRESS RESISTANCE; ZN SUPEROXIDE-DISMUTASE; INNATE IMMUNE-RESPONSE; EXTENDS LIFE-SPAN; GENE-EXPRESSION; HUMAN LONGEVITY; CALORIC RESTRICTION; INSULIN-RECEPTOR;
D O I
10.3389/fphys.2012.00106
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Human life expectancy has nearly doubled in the past century due, in part, to social and economic development, and a wide range of new medical technologies and treatments. As the number of elderly increase it becomes of vital importance to understand what factors contribute to healthy aging. Human longevity is a complex process that is affected by both environmental and genetic factors and interactions between them. Unfortunately, it is currently difficult to identify the role of genetic components in human longevity. In contrast, model organisms such as C. elegans, Drosophila, and rodents have facilitated the search for specific genes that affect lifespan. Experimental evidence obtained from studies in model organisms suggests that mutations in a single gene may increase longevity and delay the onset of age-related symptoms including motor impairments, sexual and reproductive and immune dysfunction, cardiovascular disease, and cognitive decline. Furthermore, the high degree of conservation between diverse species in the genes and pathways that regulate longevity suggests that work in model organisms can both expand our theoretical knowledge of aging and perhaps provide new therapeutic targets for the treatment of age-related disorders.
引用
收藏
页数:11
相关论文
共 199 条
[1]   Estimating disease resistance in insects:: phenoloxidase and lysozyme-like activity and disease resistance in the cricket Gryllus texensis [J].
Adamo, SA .
JOURNAL OF INSECT PHYSIOLOGY, 2004, 50 (2-3) :209-216
[2]   Regulation of life-span by germ-line stem cells in Caenorhabditis elegans [J].
Arantes-Oliveira, N ;
Apfeld, J ;
Dillin, A ;
Kenyon, C .
SCIENCE, 2002, 295 (5554) :502-505
[3]   Multiple longevity phenotypes and the transition from health to senescence [J].
Arking, R .
REVERSAL OF AGING: RESETTING THE PINEAL CLOCK, 2005, 1057 :16-27
[4]   ELEVATED PARAQUAT RESISTANCE CAN BE USED AS A BIOASSAY FOR LONGEVITY IN A GENETICALLY BASED LONG-LIVED STRAIN OF DROSOPHILA [J].
ARKING, R ;
BUCK, S ;
BERRIOS, A ;
DWYER, S ;
BAKER, GT .
DEVELOPMENTAL GENETICS, 1991, 12 (05) :362-370
[5]   Forward and reverse selection for longevity in Drosophila is characterized by alteration of antioxidant gene expression and oxidative damage patterns [J].
Arking, R ;
Burde, V ;
Graves, K ;
Hari, R ;
Feldman, E ;
Zeevi, A ;
Soliman, S ;
Saraiya, A ;
Buck, S ;
Vettraino, J ;
Sathrasala, K ;
Wehr, N ;
Levine, RL .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (02) :167-185
[6]   Aging: A biological perspective [J].
Arking, R .
AMERICAN SCIENTIST, 2003, 91 (06) :508-515
[7]   Metabolic alterations and shifts in energy allocations are corequisites for the expression of extended longevity genes in Drosophila [J].
Arking, R ;
Buck, S ;
Hwangbo, DS ;
Lane, M .
INCREASING HEALTHY LIFE SPAN: CONVENTIONAL MEASURES AND SLOWING THE INNATE AGING PROCESS, 2002, 959 :251-262
[8]  
Arking R., 2002, ANN NY ACAD SCI, V959, P463
[9]   Invertebrate models of age-related muscle degeneration [J].
Augustin, Hrvoje ;
Partridge, Linda .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2009, 1790 (10) :1084-1094
[10]   MAMMALIAN AGING, METABOLISM, AND ECOLOGY - EVIDENCE FROM THE BATS AND MARSUPIALS [J].
AUSTAD, SN ;
FISCHER, KE .
JOURNALS OF GERONTOLOGY, 1991, 46 (02) :B47-B53