Instituto Nacional de Investigaciones Nucleares, Gerencia de Ciencias Básicas, Mexico.
Radiat Res. 2013 Jun;179(6):669-73. doi: 10.1667/RR3223.1. Epub 2013 May 3.
The aim of the present study is to determine the deoxyribonucleic acid (DNA) damage by cells exposed to atmospheric pressure non-thermal plasma (APNTP). Mouse leukocytes embedded in agarose were exposed to the plasma at two different distances from a helium plasma needle outlet and during three different exposure periods. Damage was assessed by the single cell gel electrophoresis assay. The results indicate that, at 0.1 cm from the plasma needle, the exposure caused complete DNA fragmentation determined by the presence of so called "clouds". Samples exposed at 0.5 cm from the slide sample surface presented damage proportional to the exposure periods in terms of tail intensity, tail moment and "clouds" frequency. Studies performed with alkaline single cell gel electrophoresis assay to determine DNA breaks and alkali-labile sites, indicates that DNA damage produced by exposure to APNTP was caused mainly by oxidative radicals, rather than by UV light which causes cyclobutane pyrimidine dimers. These results allow us to conclude that plasma needle induced DNA breaks in mice leukocytes proportionally to exposure time.
本研究旨在确定暴露于大气压非热等离子体(APNTP)的细胞中的脱氧核糖核酸(DNA)损伤。将琼脂糖包埋的小鼠白细胞暴露于氦等离子体针出口的两个不同距离和三个不同的暴露时间的等离子体中。通过单细胞凝胶电泳测定法评估损伤。结果表明,在距等离子体针 0.1 厘米处,暴露会导致完全的 DNA 碎片化,这可以通过存在所谓的“云”来确定。在距载玻片表面 0.5 厘米处暴露的样品,其尾巴强度、尾巴矩和“云”频率与暴露时间成正比,呈现出损伤。用碱性单细胞凝胶电泳测定法进行的研究,以确定 DNA 断裂和碱不稳定部位,表明暴露于 APNTP 产生的 DNA 损伤主要是由氧化自由基引起的,而不是由引起环丁烷嘧啶二聚体的紫外线引起的。这些结果使我们得出结论,等离子体针诱导的小鼠白细胞 DNA 断裂与暴露时间成正比。