Influence of orange juice over the genotoxicity induced by alkylating agents:: an in vivo analysis

被引:40
作者
Franke, SIR
Prá, D
Erdtmann, B
Henriques, JAP
da Silva, J
机构
[1] Univ Luterana Brasil, Curso Biol, Curso Farm, Canoas, RS, Brazil
[2] Univ Santa Cruz do Sul, Curso Nutr, Dept Educ Fis & Saude, Santa Cruz do Sul, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Genotox, Ctr Biotecnol, Programa Pos Grad Biol Celular & Mol,Programa Pos, Porto Alegre, RS, Brazil
[4] Univ Caxias do Sul UCS, Inst Biotecnol, Caxias do Sul, RS, Brazil
关键词
D O I
10.1093/mutage/gei034
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There is considerable epidemiological evidence indicating an association between diets rich in fresh fruit and vegetables and a decreased incidence of cancers. Methyl methanesulfonate (MMS) and cyclophosphamide (CP) are alkylating agents that differ in their mode of action. MMS is a directly-acting, monofunctional agent, while CP is a bifunctional agent that requires metabolic activation to a reactive metabolite. To evaluate if orange juice could reduce DNA damage induced by these alkylating agents, mice were treated orally (by gavage) with MMS and CP, prior to and after treatment with orange juice. DNA damage was evaluated by the comet assay in peripheral white blood cells. Under these experimental conditions, orange juice reduced the extent of DNA damage caused by both mutagens. For MMS, the antigenotoxic effect of the orange juice was both protective (orange juice pre-treatment) and reparative (orange juice post-treatment); for CP, the effect was reparative only. The components of orange juice can have several biological effects, including acting as targets of toxicants and modulating metabolization/detoxification routes. Considering the different mechanisms of the action of the two drugs, different protective effects are suggested. These results demonstated the ability of the in vivo comet assay to detect in vivo modulation of MMS and CP mutagenicity by orange juice.
引用
收藏
页码:279 / 283
页数:5
相关论文
共 42 条
[1]   Repair of iron-induced DNA oxidation by the flavonoid myricetin in primary rat hepatocyte cultures [J].
Abalea, V ;
Cillard, J ;
Dubos, MP ;
Sergent, O ;
Cillard, P ;
Morel, I .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (11-12) :1457-1466
[2]   Flavanone absorption after naringin, hesperidin, and citrus administration [J].
Ameer, B ;
Weintraub, RA ;
Johnson, JV ;
Yost, RA ;
Rouseff, RL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (01) :34-40
[3]   O6-alkylguanine-DNA alkyltransferase:: influence on susceptibility to the genetic effects of alkylating agents [J].
Kyrtopoulos, SA .
TOXICOLOGY LETTERS, 1998, 103 :53-57
[4]   The causes and prevention of cancer: The role of environment [J].
Ames, BN ;
Gold, LS .
BIOTHERAPY, 1998, 11 (2-3) :205-220
[5]   DNA damage from micronutrient deficiencies is likely to be a major cause of cancer [J].
Ames, BN .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 475 (1-2) :7-20
[6]   Abasic sites in DNA:: repair and biological consequences in Saccharomyces cerevisiae [J].
Boiteux, S ;
Guillet, M .
DNA REPAIR, 2004, 3 (01) :1-12
[7]  
Brozmanová J, 2001, NEOPLASMA, V48, P85
[8]   Increased DNA double strand breakage is responsible for sensitivity of the pso3-1 mutant of Saccharomyces cerevisiae to hydrogen peroxide [J].
Brozmanová, J ;
Vlcková, V ;
Farkasová, E ;
Dudás, A ;
Vlasáková, D ;
Chovanec, M ;
Mikulovská, Z ;
Fridrichová, I ;
Saffi, J ;
Henriques, JAP .
MUTATION RESEARCH-DNA REPAIR, 2001, 485 (04) :345-355
[9]   THE KINETICS OF REPAIR OF OXIDATIVE DNA-DAMAGE (STRAND BREAKS AND OXIDIZED PYRIMIDINES) IN HUMAN-CELLS [J].
COLLINS, AR ;
MA, AG ;
DUTHIE, SJ .
MUTATION RESEARCH-DNA REPAIR, 1995, 336 (01) :69-77
[10]   Novel repair action of vitamin C upon in vivo oxidative DNA damage [J].
Cooke, MS ;
Evans, MD ;
Podmore, ID ;
Herbert, KE ;
Mistry, N ;
Mistry, P ;
Hickenbotham, PT ;
Hussieni, A ;
Griffiths, HR ;
Lunec, J .
FEBS LETTERS, 1998, 439 (03) :363-367