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暴露于苯并[a]芘的绿唇贻贝(翡翠贻贝)中的DNA加合物形成与DNA链断裂:剂量和时间依赖性关系

DNA adduct formation and DNA strand breaks in green-lipped mussels (Perna viridis) exposed to benzo[a]pyrene: dose- and time-dependent relationships.

作者信息

Ching E W, Siu W H, Lam P K, Xu L, Zhang Y, Richardson B J, Wu R S

机构信息

Department of Biology and Chemistry, Centre for Coastal Pollution and Conservation, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong SAR, People's Republic of China.

出版信息

Mar Pollut Bull. 2001 Jul;42(7):603-10. doi: 10.1016/s0025-326x(00)00209-5.

Abstract

Green-lipped mussels, Perna viridis, were exposed to 0, 0.3, 3 and 30 micrograms l-1 (nominal concentrations) B[a]P under laboratory conditions over a period of 24 days. Mussels were collected on day 0, 1, 3, 6, 12, 18 and 24, and the levels of DNA adducts and DNA strand breaks in their hepatopancreas tissues monitored. Mussels exposed to 0.3 and 3 micrograms l-1 B[a]P showed marked increases in strand breaks after 1 day of exposure. DNA strand break levels in these mussels remained high and significantly different from the control values until day 3 for the 0.3 microgram l-1 treatment group, and day 6 for the 3 micrograms l-1 treatment group. This was followed by a gradual reduction in strand breaks. After 12 days, the levels of both groups had returned to the same level as that of the control. No increase in DNA strand breaks was observable in mussels exposed to 30 micrograms l-1 B[a]P in the first 12 days of exposure, but a significant increase was observed from day 12 to day 24. Increasing B[a]P concentrations resulted in elevated DNA adduct levels after 3-6 days of exposure, but this pattern of dose-related increase disappeared after 12 days. These results indicate that a better understanding of the complex interactions between exposure levels and durations is crucially important before DNA adduct levels and DNA strand breaks in P. viridis can be used as effective biomarkers for monitoring genotoxicants in marine waters.

摘要

在实验室条件下,将绿唇贻贝(Perna viridis)暴露于浓度为0、0.3、3和30微克/升(标称浓度)的苯并[a]芘中,持续24天。在第0、1、3、6、12、18和24天收集贻贝,并监测其肝胰腺组织中的DNA加合物水平和DNA链断裂情况。暴露于0.3和3微克/升苯并[a]芘的贻贝在暴露1天后,链断裂显著增加。对于0.3微克/升处理组,直至第3天,以及对于3微克/升处理组,直至第6天,这些贻贝中的DNA链断裂水平一直很高,且与对照组值有显著差异。随后链断裂逐渐减少。12天后,两组的水平均恢复到与对照组相同的水平。在暴露的前12天,暴露于30微克/升苯并[a]芘的贻贝中未观察到DNA链断裂增加,但在第12天至第24天观察到显著增加。暴露3 - 6天后,随着苯并[a]芘浓度的增加,DNA加合物水平升高,但这种剂量相关增加的模式在12天后消失。这些结果表明,在将绿唇贻贝中的DNA加合物水平和DNA链断裂用作监测海水中遗传毒性物质的有效生物标志物之前,更好地理解暴露水平和持续时间之间的复杂相互作用至关重要。

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