Vodicka P, Vodicková L, Trejbalová K, Srám R J, Hemminki K
Institute of Experimental Medicine, Czech Academy of Sciences, Prague.
Carcinogenesis. 1994 Sep;15(9):1949-53. doi: 10.1093/carcin/15.9.1949.
A modified 32P-postlabelling method was used for the detection of styrene-specific DNA adducts in lamination workers. The persistence of O6-styrene DNA adducts was studied in DNA from lymphocytes and granulocytes of an exposed and a control group. We compared O6-adduct levels obtained from a sampling prior to vacation, after 2 weeks of vacation and after an additional 1 month of work. In granulocytes, there was no significant difference in adduct levels between the control and the exposed groups in any individual samplings. In lymphocytes of laminators the detected adduct levels were significantly higher (5.4 adducts/10(8) nucleotides) than those in the controls (1.0 adduct/10(8) nucleotides). The 2 week interruption of exposure did not influence the total O6-adduct level (4.9 adducts/10(8) nucleotides in the first sampling versus 5.1 adducts/10(8) nucleotides in the second), indicating very slow removal of the specific O6-styrene adducts from DNA.
采用改良的³²P后标记法检测层压工人中苯乙烯特异性DNA加合物。研究了暴露组和对照组淋巴细胞及粒细胞DNA中O6-苯乙烯DNA加合物的持久性。我们比较了休假前、休假2周后以及再工作1个月后的采样中获得的O6-加合物水平。在粒细胞中,任何一次单独采样中,对照组和暴露组的加合物水平均无显著差异。在层压工人的淋巴细胞中,检测到的加合物水平(5.4个加合物/10⁸个核苷酸)显著高于对照组(1.0个加合物/10⁸个核苷酸)。2周的暴露中断并未影响总的O6-加合物水平(第一次采样为4.9个加合物/10⁸个核苷酸,第二次采样为5.1个加合物/10⁸个核苷酸),这表明DNA中特异性O6-苯乙烯加合物的清除非常缓慢。