Sorsa M, Hemminki K, Vainio H
Teratog Carcinog Mutagen. 1982;2(2):137-50. doi: 10.1002/1520-6866(1990)2:2<137::aid-tcm1770020204>3.0.co;2-4.
Occupational exposure to chemical mutagens can be monitored by measuring the chemical interaction that occurs between the exposing agent and biologic macro-molecules. Such interaction is detectable in the body fluids as adducts of, e.g., DNA or glutathione. The mutagenic compounds or their metabolites can also be measured from urine samples, by use of bacterial mutagenicity assays. Much basic research is still needed before these methodologies are applicable for routine monitoring. At present, cytogenetic approaches appear to be nearest to routine surveillance in detecting early biologic effects in exposed humans. Studies on structural chromosome aberrations or sister chromatid exchanges (SCEs) in peripheral blood lymphocytes obviously detect different molecular injuries, and the results from in vivo occupational exposures do not necessarily correlate. Somatic chromosome damage should always be considered a warning sign of potentially adverse effects, and such damage should lead to decreased exposure to the causative agent.
职业性接触化学诱变剂可通过测量暴露剂与生物大分子之间发生的化学相互作用来进行监测。这种相互作用在体液中可检测为例如DNA或谷胱甘肽的加合物。诱变化合物或其代谢物也可通过细菌诱变性测定法从尿液样本中进行测量。在这些方法适用于常规监测之前,仍需要进行大量基础研究。目前,细胞遗传学方法似乎在检测接触人群的早期生物学效应方面最接近常规监测。对外周血淋巴细胞中的结构染色体畸变或姐妹染色单体交换(SCE)的研究显然检测到不同的分子损伤,并且体内职业暴露的结果不一定相关。体细胞染色体损伤应始终被视为潜在不良反应的警示信号,并且这种损伤应导致减少接触致病因子。