Superoxide dismutase activities in long-lived Drosophila melanogaster females:: chico1 genotypes and dietary dilution

被引:25
作者
Kabil, Hadise
Partridge, Linda
Harshman, Lawrence G. [1 ]
机构
[1] Univ Nebraska, Sch Biol Sci, Lincoln, NE 68588 USA
[2] UCL, Dept Biol, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会;
关键词
Drosophila; dietary restriction; caloric restriction; insulin signaling; superoxide dismutase (SOD); antioxidants; longevity;
D O I
10.1007/s10522-006-9065-3
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
Superoxide dismutase (SOD) activities were determined for dietary dilution conditions that extend the life span of Drosophila melanogaster. The hypothesis motivating this research was that elevated SOD activity is associated with increased life span resulting from flies being held on a restricted diet. SOD activities were also measured for chico (1) which is a mutation in the insulin receptor substrate protein gene associated with life span extension. This allowed us to confirm the results of (Clancy et al. 2001) and extend the results by measuring CuZn SOD and Mn SOD activities in addition to the previously determined overall SOD activity. If the same form of SOD activity (CuZn SOD or Mn SOD) was elevated on the dilute diet that extends life span and in the long lived chico (1) homozygotes, then it would suggest that life span extension by dietary restriction and by insulin signaling mutations has a similar underlying mechanism. However, overall SOD activity, and CuZn SOD or Mn SOD activities did not differ among the diets tested. As observed previously (Clancy et al. 2001), overall SOD activity was elevated in chico (1) homozygotes compared to the heterozygote or wild type. Results from the present study indicate that elevated CuZn SOD activity, not Mn SOD, is the basis for the relatively high level of SOD activity in the chico (1) homozygotes.
引用
收藏
页码:201 / 208
页数:8
相关论文
共 37 条
[1]   Oocyte maturation and ovariole number in lines of Drosophila melanogaster selected for postponed senescence [J].
Carlson, KA ;
Nusbaum, TJ ;
Rose, MR ;
Harshman, LG .
FUNCTIONAL ECOLOGY, 1998, 12 (04) :514-520
[2]   Female fitness in Drosophila melanogaster: An interaction between the effect of nutrition and of encounter rate with males [J].
Chapman, T ;
Partridge, L .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1996, 263 (1371) :755-759
[3]   Extension of life-span by loss of CHICO, a Drosophila insulin receptor substrate protein [J].
Clancy, DJ ;
Gems, D ;
Harshman, LG ;
Oldham, S ;
Stocker, H ;
Hafen, E ;
Leevers, SJ ;
Partridge, L .
SCIENCE, 2001, 292 (5514) :104-106
[4]  
Fabrizio P, 2003, GENETICS, V163, P35
[5]   Regulation of longevity and stress resistance by Sch9 in yeast [J].
Fabrizio, P ;
Pozza, F ;
Pletcher, SD ;
Gendron, CM ;
Longo, VD .
SCIENCE, 2001, 292 (5515) :288-290
[6]   CALORIC RESTRICTION, AGING, AND ANTIOXIDANT ENZYMES [J].
FEUERS, RJ ;
WEINDRUCH, R ;
HART, RW .
MUTATION RESEARCH, 1993, 295 (4-6) :191-200
[7]  
FRIEDMAN DB, 1988, GENETICS, V118, P75
[8]   Insulin/IGF signalling and ageing: seeing the bigger picture [J].
Gems, D ;
Partridge, L .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2001, 11 (03) :287-292
[9]   AGING - A THEORY BASED ON FREE-RADICAL AND RADIATION-CHEMISTRY [J].
HARMAN, D .
JOURNALS OF GERONTOLOGY, 1956, 11 (03) :298-300
[10]   Genetics of lifespan in C-elegans:: molecular diversity, physiological complexity, mechanistic simplicity [J].
Hekimi, S ;
Burgess, J ;
Bussière, F ;
Meng, Y ;
Bénard, C .
TRENDS IN GENETICS, 2001, 17 (12) :712-718