Genotoxic assessment in peripheral blood lymphocytes of post-polio individuals using sister chromatid exchange analysis and micronucleus assay

被引:3
|
作者
Bhattacharya, Saurabh Kumar [1 ]
Saraswathy, Radha [1 ]
Sivakumar, E. [2 ]
机构
[1] VIT Univ, Sch Biosci & Technol, Div Biomol & Genet, Vellore 632014, Tamil Nadu, India
[2] Govt Vellore Med Coll & Hosp, Vellore, Tamil Nadu, India
关键词
post-polio syndrome; chromosomal aberrations; sister chromatid exchange; micronucleus; cytochalasin B; 5-bromo-2-deoxyuridine; DEOXYRIBONUCLEIC-ACID REPLICATION; CHROMOSOME-ABERRATIONS; METAPHASE CHROMOSOMES; SODIUM-PHOSPHATE; BUDR; POLIOMYELITIS; FREQUENCY; DAMAGE; VIRUS; DNA;
D O I
10.1177/0960327110376983
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Environmental pollution is a complex issue because of the diversity of anthropogenic agents, both chemical and physical, that have been detected and catalogued. The consequences to biota from exposure to genotoxic agents present an additional problem because of the potential for these agents to produce adverse change at the cellular and organism levels. Past studies in virus have focused on structural damage to the DNA of environmental species that may occur after exposure to genotoxic agents and the use of this information to document exposure and to monitor remediation. In an effort to predict effects at the population, community and ecosystem levels, in the present study, we attempt to characterize damage occurring through genotoxic agents like 5-bromo-2-deoxyuridine, BrdU, using sister chromatid exchange technique and the formation of micronuclei (MN) in the peripheral lymphocytes of the post-polio syndrome sequelae affected by poliovirus. Analysis of structural chromosomal aberrations (CAs) and involvement of the specific chromosome break were pursued in this study. They revealed a significantly higher incidence of CAs (chromatid and chromosome breaks) in patients compared with controls, where the specific chromosome break has emerged as specific. Also, the maximum numbers of breaks were found to be in chromosome 1 at the position 1p36.1. The results also suggest a correlation between CAs and content of MN.
引用
收藏
页码:636 / 648
页数:13
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