DNA Damage Induced by Copper on Erythrocytes of Gilthead Sea Bream Sparus aurata and Mollusk Scapharca inaequivalvis
详细信息    查看全文
  • 作者:Rosita Gabbianelli ; Giulio Lupidi ; Milena Villarini and Giancarlo Falcioni
  • 刊名:Archives of Environmental Contamination and Toxicology
  • 出版年:2003
  • 出版时间:October 2003
  • 年:2003
  • 卷:45
  • 期:3
  • 页码:350-356
  • 全文大小:203 KB
  • 刊物类别:Earth and Environmental Science
  • 刊物主题:Environment
    Terrestrial Pollution
    Agriculture
    Ecology
    Forestry
    Environment
    Soil Science and Conservation
  • 出版者:Springer New York
  • ISSN:1432-0703
文摘
Heavy metal pollution in rivers and its impact on aquatic ecosystems is a dynamic process. Fish are ideal indicators of heavy metal contamination in aquatic systems because they occupy different trophic levels and are of different sizes and ages. In particular, copper is an essential trace metal for living organisms and it is present in all natural waters and sediments. In this paper, we report data on the effect of copper on DNA erythrocytes from the teleost gilthead sea bream Sparus aurata and the bivalve mollusk Scapharca inaequivalvis. In particular, the effect of 0.1 ppm of Cu2+ on the nucleated erythrocytes was analyzed using the comet assay. This test is a promising tool for estimation of DNA damage at the single cell level. The data obtained show that the in vivo treatment with 0.1 ppm of copper increased the susceptibility of DNA to be damaged. Exposure to Cu2+ produces a more evident effect on Sparus aurata, as all three comet parameters significantly increased (tail length, tail intensity, and tail moment). The higher comet parameters measured in Scapharca inaequivalvis compared to Sparus aurata could be due to the difference in stability of the respective hemoglobins. The comet assay could represent a useful test to evaluate the biological consequences of environmental contamination by metals on marine organisms.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700