Storer R D, Conolly R B
Anal Biochem. 1984 Nov 1;142(2):351-9. doi: 10.1016/0003-2697(84)90476-7.
An in vivo-in vitro alkaline DNA unwinding assay for single-strand breaks and/or alkali-labile lesions in hepatic DNA is described. The assay involves isolation of hepatic nuclei from mice, alkaline denaturation and unwinding of hepatic DNA, separation of single- and double-stranded DNA by hydroxylapatite batch chromatography, and quantitation of DNA in chromatographic fractions by a fluorometric assay. The method allows for the sensitive detection of hepatic DNA damage following in vivo administration of xenobiotics. Using this procedure, DNA fragmentation was demonstrated in alkali after administration of as little as 0.5 mg/kg of N-nitrosodimethylamine (DMN) to male B6C3F1 mice. A comparison of this technique with a similar alkaline sucrose density gradient centrifugation assay demonstrated comparable limits of sensitivity for the two procedures.
本文描述了一种用于检测肝脏DNA中单链断裂和/或碱不稳定损伤的体内-体外碱性DNA解旋试验。该试验包括从小鼠中分离肝细胞核、肝DNA的碱性变性和解旋、通过羟基磷灰石柱层析分离单链和双链DNA,以及通过荧光测定法定量层析组分中的DNA。该方法能够灵敏地检测体内给予外源化学物后肝脏DNA的损伤。使用该程序,在给雄性B6C3F1小鼠给予低至0.5mg/kg的N-亚硝基二甲胺(DMN)后,在碱性条件下证实了DNA片段化。将该技术与类似的碱性蔗糖密度梯度离心试验进行比较,结果表明这两种方法的灵敏度极限相当。