Assessment of DNA damage in spleen, bone marrow, and peripheral blood from malnourished rats by single cell gel electrophoresis assay

被引:19
作者
Cortés, E [1 ]
González, C [1 ]
Betancourt, M [1 ]
Ortiz, R [1 ]
机构
[1] Univ Autonoma Metropolitana Iztapalapa, Dept Ciencias Salud, Mexico City 09340, DF, Mexico
来源
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS | 2001年 / 21卷 / 03期
关键词
severe malnutrition; DNA damage; tissues of rat; rat lymphocytes; experimental malnutrition; comet assay;
D O I
10.1002/tcm.1012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Severe malnutrition is widely distributed throughout the world and exhibits a high prevalence in developing countries. Experimental malnutrition models have been useful to study the effects of malnutrition at early ages. The purpose of this study was to determine if severe malnutrition induced during lactation in rats increases DNA damage in spleen, peripheral blood, and bone marrow cells, as well as in isolated lymphocytes or lymphoid cells from the same tissues. These cells were obtained from malnourished rats at weaning (21 days of age). DNA damage was estimated by using the alkaline single cell electrophoresis assay. The results obtained in this study indicate that malnutrition is associated with a significant increase in DNA damage in all cell types that were studied in malnourished rats. The analysis of the length of DNA migration and dispersion coefficient showed that some cell types were more susceptible to DNA damage related with malnutrition. The damage observed could be due to the deficiency of several essential nutrients required for protein synthesis that are associated with DNA integrity, impaired DNA repair mechanisms, and/or to the unavailability of molecules necessary to protect the cells against DNA oxidative damage. This damage may produce negative effects for the further development of the organism, since bone marrow is the main site of hematopoiesis and spleen is an important lymphopoietic organ. Also, the increased level of DNA damage in peripheral blood lymphocytes and leukocytes could be related to negative effects such as a deficient immune response. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:231 / 247
页数:17
相关论文
共 41 条
[1]   About the oxidative stress status in children with kwashiorkor [J].
Albrecht, R ;
Pelissier, MA .
FOOD AND CHEMICAL TOXICOLOGY, 1995, 33 (12) :1081-1083
[2]  
AltamiranoLozano M, 1996, TERATOGEN CARCIN MUT, V16, P7, DOI 10.1002/(SICI)1520-6866(1996)16:1<7::AID-TCM2>3.0.CO
[3]  
2-M
[4]   CHROMOSOMAL-ABNORMALITIES IN STARVED AND MARGINALLY MALNOURISHED RATS AND INUTERO UPON REHABILITATION [J].
ALU, V ;
MURTHY, PB .
EXPERIENTIA, 1993, 49 (03) :258-262
[5]   GLUTATHIONE AND ASSOCIATED ANTIOXIDANT SYSTEMS IN PROTEIN-ENERGY MALNUTRITION - RESULTS OF A STUDY IN NIGERIA [J].
BECKER, K ;
LEICHSENRING, M ;
GANA, L ;
BREMER, HJ ;
SCHIRMER, RH .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (02) :257-263
[6]   FREQUENCY OF SISTER-CHROMATID EXCHANGE (SCE) IN BONE-MARROW CELLS OF SEVERELY MALNOURISHED ANIMALS DURING EARLY LIFE [J].
BETANCOURT, M ;
BALVANERA, P ;
ORTIZ, R .
MUTATION RESEARCH, 1986, 175 (01) :29-31
[7]   ASSESSMENT OF DNA-DAMAGE IN LEUKOCYTES FROM INFECTED AND MALNOURISHED CHILDREN BY SINGLE-CELL GEL-ELECTROPHORESIS COMET ASSAY [J].
BETANCOURT, M ;
ORTIZ, R ;
GONZALEZ, C ;
PEREZ, P ;
CORTES, L ;
RODRIGUEZ, L ;
VILLASENOR, L .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 331 (01) :65-77
[8]  
CRAVIOTO J, 1985, NUTR DESARROLLO MENT
[9]  
DEMELLO MAR, 1994, BRAZ J MED BIOL RES, V27, P2461
[10]   2-nitropropane-induced DNA damage in rat bone marrow [J].
Deng, XS ;
Tuo, JS ;
Poulsen, HE ;
Loft, S .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1997, 391 (03) :165-169