Parodi S, Balbi C, Taningher M, Abelmoschi M L, Pala M, Parodi G, Santi L
Toxicol Lett. 1982 Mar;10(4):351-8. doi: 10.1016/0378-4274(82)90229-6.
DNA damage induced by dimethylsulfate (DMS) was measured with a new oscillating crucible viscometer, having a U-shaped circular channel. Rat liver nuclei were treated in vitro. Viscosity was measured by lysing nuclei in an aklaline lysing solution (pH 12.5; 25 degrees C). Nuclei were lysed immediately in the viscometer and released DNA started to uncoil. In control samples the viscosity increased very slowly with time, reaching a maximum only after about 8 h. A progressively more rapid increase in viscosity was seen with increasing concentrations of DMS. The time of DNA disentanglement was sensitive to about 30 times less breaks than the alkaline elution assay.
用一种带有U形圆形通道的新型振荡坩埚粘度计测量硫酸二甲酯(DMS)诱导的DNA损伤。大鼠肝细胞核在体外进行处理。通过在碱性裂解溶液(pH 12.5;25℃)中裂解细胞核来测量粘度。细胞核在粘度计中立即裂解,释放出的DNA开始解旋。在对照样品中,粘度随时间增加非常缓慢,仅在约8小时后达到最大值。随着DMS浓度的增加,粘度增加得越来越快。DNA解缠结的时间比碱性洗脱试验对大约少30倍的断裂敏感。