'The effect of micronutrients on superoxide dismutase in senescent fibroblasts'

被引:9
作者
Al-Sheikh, Yazeed A. [1 ]
Ghneim, Hazem K. [1 ]
机构
[1] King Saud Univ, Dept Clin Lab Sci, Chair Med & Mol Genet, Coll Appl Med Sci, Riyadh 11433, Saudi Arabia
关键词
superoxide dismutases; senescent skin fibroblasts; Zn; Cu; Mn supplementation; HUMAN SKIN FIBROBLASTS; MITOCHONDRIAL-DNA MUTATION; AGE-RELATED-CHANGES; GLUTATHIONE-PEROXIDASE ACTIVITY; OXIDATIVE STRESS; ANTIOXIDANT ENZYMES; HYDROGEN-PEROXIDE; GENE-EXPRESSION; ZINC SUPPLEMENTATION; EPITHELIAL-CELLS;
D O I
10.1002/cbf.1761
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
The specific activities of zinc/copper (Zn/Cu)-superoxide dismutase (SOD-1) and manganese (Mn)-superoxide dismutase (SOD-2) were assayed in young passage 5 fibroblasts and in serially subcultured cells that were characterized as senescent at passages 15-35. SOD-1 and SOD-2 activities did not significantly change in senescent and young cells cultured in either routine medium [minimum essential medium 1 (MEM1)], or in Zn, Cu and Mn supplemented medium (MEM2) containing normal human plasma levels of the cations. SOD-1 and SOD-2 activities, however, underwent parallel progressive significant activity increases in senescent passage 20 and 25 cells, which peaked in value in passage 30 and 35 cells subcultured in supplemented medium (MEM3) containing triple human plasma levels of the cations. Concurrently, superoxide radical generation rates underwent progressive significant increases in senescent passage 15-25 cells, which peaked in value in passage 30 and 35 cells subcultured in MEM1 or MEM2. These rates, however, were significantly lowered in senescent cells subcultured in MEM3. We infer that it was only possible to significantly stimulate SOD-1 and SOD-2 activities in senescent MEM3 cultured cells enabling them to combat oxidative stress. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:384 / 393
页数:10
相关论文
共 60 条
[1]  
ALLEN RG, 1995, J CELL PHYSIOL, V165, P576
[2]  
Allen RG, 1999, J CELL PHYSIOL, V180, P114, DOI 10.1002/(SICI)1097-4652(199907)180:1<114::AID-JCP13>3.0.CO
[3]  
2-0
[4]  
[Anonymous], 1974, Clinical chemistry principles and techniques, seconded
[5]   Selenium deficiency in tissue culture: Implications for oxidative metabolism [J].
Baker, RD ;
Baker, SS ;
Rao, R .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1998, 27 (04) :387-392
[6]   The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   Premature induction of aging in sublethally H2O2-treated young MRC5 fibroblasts correlates with increased glutathione peroxidase levels and resistance to DNA breakage [J].
Caldini, R ;
Chevanne, M ;
Mocali, A ;
Tombaccini, D ;
Paoletti, F .
MECHANISMS OF AGEING AND DEVELOPMENT, 1998, 105 (1-2) :137-150
[9]   AGE-RELATED-CHANGES IN CU,ZN SUPEROXIDE-DISMUTASE, SE-DEPENDENT AND SE-INDEPENDENT GLUTATHIONE-PEROXIDASE AND CATALASE ACTIVITIES IN SPECIFIC AREAS OF RAT-BRAIN [J].
CIRIOLO, MR ;
FISKIN, K ;
DEMARTINO, A ;
CORASANITI, MT ;
NISTICO, G ;
ROTILIO, G .
MECHANISMS OF AGEING AND DEVELOPMENT, 1991, 61 (03) :287-297
[10]   Elevation of manganese superoxide dismutase gene expression by thioredoxin [J].
Das, KC ;
Lewis-Molock, Y ;
White, CW .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 17 (06) :713-726