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低浓度苯乙烯暴露工人白细胞中DNA单链断裂随暴露剂量增加。

Exposure dependent increase in DNA single strand breaks in leucocytes from workers exposed to low concentrations of styrene.

作者信息

Walles S A, Edling C, Anundi H, Johanson G

机构信息

Department of Toxicology, National Institute of Occupational Health, Solna, Sweden.

出版信息

Br J Ind Med. 1993 Jun;50(6):570-4. doi: 10.1136/oem.50.6.570.

Abstract

Single strand breaks in DNA were monitored in leucocytes from 17 men occupationally exposed to styrene. Personal air monitoring was carried out during one workday with two diffusion samplers and a portable photoionisation detector placed in the breathing zone. Exposure to styrene was also monitored by analysing styrene in blood and urine and mandelic acid in urine. Single strand breaks were measured in leucocytes by the alkaline elution technique. The biological samples were collected before a shift, at the end of a shift, and the next morning, before the next shift. An exposure dependent increase in single strand breaks was seen at the end of a shift but not before a shift or the next morning. Linear regression analysis indicated that the amount of DNA damage was roughly doubled after eight hours of exposure to 18 ppm styrene or at a urine concentration of 240 mg mandelic acid/g creatinine compared with the damage in non-exposed men. This study indicates that monitoring of single strand breaks with the alkaline elution technique may be a sensitive marker of genotoxic effects. To our knowledge, this is the first time that such a marker has been shown to correlate with exposure to less than 20 ppm styrene.

摘要

对17名职业性接触苯乙烯的男性白细胞中的DNA单链断裂情况进行了监测。在一个工作日期间,使用两个扩散采样器和一个置于呼吸区的便携式光离子化探测器进行个人空气监测。还通过分析血液和尿液中的苯乙烯以及尿液中的扁桃酸来监测苯乙烯暴露情况。采用碱性洗脱技术测量白细胞中的单链断裂情况。生物样本在轮班前、轮班结束时以及第二天早晨、下一轮班前采集。在轮班结束时观察到单链断裂随暴露增加,但在轮班前或第二天早晨未观察到。线性回归分析表明,与未暴露男性相比,暴露于18 ppm苯乙烯8小时后或尿液中扁桃酸浓度为240 mg/g肌酐时,DNA损伤量大约增加了一倍。本研究表明,用碱性洗脱技术监测单链断裂可能是遗传毒性效应的一个敏感标志物。据我们所知,这是首次表明这种标志物与低于20 ppm苯乙烯的暴露相关。

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本文引用的文献

1
Single-strand breaks in DNA of various organs of mice induced by styrene and styrene oxide.
Cancer Lett. 1983 Nov;21(1):9-15. doi: 10.1016/0304-3835(83)90076-9.
3
Covalent binding of styrene and styrene-7,8-oxide to plasma proteins, hemoglobin and DNA in the mouse.
Chem Biol Interact. 1985 Oct;55(1-2):63-73. doi: 10.1016/s0009-2797(85)80120-4.
8
The genetic toxicology of styrene and styrene oxide.苯乙烯和氧化苯乙烯的遗传毒理学。
Mutat Res. 1991 Mar;257(2):107-26. doi: 10.1016/0165-1110(91)90021-m.

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