Grover P, Banu B S, Devi K D, Begum S
Toxicology Unit, Biology Division, Indian Institute of Chemical Technology, 500007, Andhra Pradesh, Hyderabad, India.
Toxicology. 2001 Oct 30;167(3):191-7. doi: 10.1016/s0300-483x(01)00469-3.
DNA damage induced by Mercuric chloride (HgCl2) in leucocytes of Wistar albino male rats has been studied in vivo. The comet assay or the alkaline single cell gel electrophoresis (SCGE) assay was used to measure the DNA damage. The rats were administered orally with doses ranging from 0.0054, 0.0108, 0.0216, 0.0432 to 0.0864 mg/kg body weight (b.wt.) of HgCl2. The assay was performed on whole blood at 24, 48, 72 h, 1st and 2nd week. The reason leucocytes were used was to reflect biomarker studies in humans. A significant increase in mean comet tail length indicating DNA damage was observed at all time intervals with HgCl2 except in 2nd week post treatment when compared to controls. The mean comet tail length revealed a clear dose dependent increase from 0.0054 to 0.0432 mg/kg b.wt. A maximum increase in mean comet tail length was observed at 0.0432 mg/kg b.wt. 24 h after treatment. From 48 h post treatment, the mean comet tail lengths of all the doses gradually decreased and by week 2 of post treatment, they had approached control levels, pointing to repair of the damaged DNA. These findings suggest that the comet assay is a highly sensitive technique to study DNA damage caused by metals.
已在体内研究了氯化汞(HgCl2)对Wistar白化雄性大鼠白细胞诱导的DNA损伤。采用彗星试验或碱性单细胞凝胶电泳(SCGE)试验来测量DNA损伤。给大鼠口服剂量范围为0.0054、0.0108、0.0216、0.0432至0.0864mg/kg体重(b.wt.)的HgCl2。在24、48、72小时、第1周和第2周对全血进行该试验。使用白细胞的原因是为了反映人类的生物标志物研究。与对照组相比,除治疗后第2周外,在所有时间间隔观察到HgCl2导致平均彗星尾长显著增加,表明存在DNA损伤。平均彗星尾长显示从0.0054至0.0432mg/kg b.wt.呈明显的剂量依赖性增加。在治疗后24小时,0.0432mg/kg b.wt.时观察到平均彗星尾长增加最多。治疗后48小时起,所有剂量的平均彗星尾长逐渐下降,到治疗后第2周,它们已接近对照水平,表明受损DNA得到修复。这些发现表明彗星试验是研究金属引起的DNA损伤的一种高度敏感的技术。