Devi K D, Banu B S, Grover P, Jamil K
Toxicology Unit, Biology and Biotechnology Division, Indian Institute of Chemical Technology, Hyderabad, India.
Toxicology. 2000 Apr 14;145(2-3):195-201. doi: 10.1016/s0300-483x(00)00154-2.
Single stranded DNA breakage induced by lead nitrate in mice has been studied in vivo using alkaline single cell gel electrophoresis (comet assay). Mice were administered orally 0.7, 1.4, 2.8, 5.6, 11. 2, 22.4, 44.8 and 89.6 mg/kg body weight of lead nitrate and the assay was performed on whole blood at 24, 48, 72 h, 1st and 2nd week. Significant increase in mean tail-length of DNA was observed at all time intervals after treatment with lead nitrate when compared to controls. The mean tail-length did not show a dose-related increase and the elevation in the mean tail-length was of a fluctuating type. Increase in mean tail-lengths clearly gives evidence that lead nitrate causes DNA damage effectively. The study indicates that the alkaline comet assay is a sensitive and rapid method to detect DNA damage caused by heavy metals.
已在体内使用碱性单细胞凝胶电泳(彗星试验)研究了硝酸铅诱导的小鼠单链DNA断裂。给小鼠口服0.7、1.4、2.8、5.6、11.2、22.4、44.8和89.6mg/kg体重的硝酸铅,并在24、48、72小时、第1周和第2周对全血进行检测。与对照组相比,用硝酸铅处理后的所有时间间隔均观察到DNA平均尾长显著增加。平均尾长未显示出剂量相关的增加,且平均尾长的升高呈波动型。平均尾长的增加清楚地证明硝酸铅有效地导致了DNA损伤。该研究表明,碱性彗星试验是检测重金属引起的DNA损伤的一种灵敏且快速的方法。