Lee W R, Abrahamson S, Valencia R, von Halle E S, Würgler F E, Zimmering S
Mutat Res. 1983 Oct;123(2):183-279. doi: 10.1016/0165-1110(83)90025-8.
The test for sex-linked recessive lethals (SLRL) in Drosophila melanogaster has been used to detect induced mutations since 1927. The advantage of the test for both screening and hazard evaluation is its objectivity in testing for transmissible mutations in the germ cells of a eukaryote. Statistical criteria for both positive and negative mutagenicity at the highest concentration tested under a particular exposure condition were developed by the Work Group, and a recommended protocol for future testing was agreed upon. For 421 compounds there were sufficient data available in the literature for analysis; 198 compounds were found to be positive and 46 negative at the highest concentration tested. Most experiments had been done for objectives of pure research rather than for deliberately screening for mutagenicity, although many of the 421 chemicals were selected for testing because of suspected mutagenicity. Therefore, the statement of 198 positive and 46 negative should not be taken as an example of the proportion of mutagens in the environment. In three sets of experiments with D. melanogaster that were done specifically for screening, one involving 40 compounds for the Environmental Protection Agency (EPA), the others involving 13 for the Food and Drug Administration (FDA), only 6 mutagens were discovered. After completion of the classification of compounds according to their response in the SLRL test, the compounds were classified as to their carcinogenic response according to the list of Griesemer and Cueto (1980). There were 62 compounds that could be classified as positive or negative for both carcinogenesis and mutagenesis. Of the 62 compounds, there was agreement between the carcinogenesis and mutagenesis classification in 56 (50 positive and 6 negative), or 90% would have been correctly classified as to carcinogenesis from only the SLRL test. Because of inadequate sample size, 177 compounds could not be classified as positive or negative according to the statistical criteria established by the Work Group. This large number of inadequately tested compounds reflects the fact that many of the experiments were not done for screening. Further work is needed on the compounds with inadequate sample size.(ABSTRACT TRUNCATED AT 400 WORDS)
自1927年以来,黑腹果蝇性连锁隐性致死(SLRL)试验一直用于检测诱发突变。该试验在筛选和危害评估方面的优势在于,它在检测真核生物生殖细胞中的可传递突变时具有客观性。工作组制定了在特定暴露条件下最高测试浓度下阳性和阴性致突变性的统计标准,并商定了未来测试的推荐方案。对于421种化合物,文献中有足够的数据可供分析;在最高测试浓度下,发现198种化合物呈阳性,46种呈阴性。大多数实验是出于纯研究目的进行的,而不是为了故意筛选致突变性,尽管421种化学物质中有许多因其疑似致突变性而被选来进行测试。因此,198种阳性和46种阴性的说法不应被视为环境中诱变剂比例的一个例子。在专门为筛选而进行的三组黑腹果蝇实验中,一组涉及为美国环境保护局(EPA)测试的40种化合物,其他两组分别涉及为美国食品药品监督管理局(FDA)测试的13种化合物,仅发现了6种诱变剂。根据化合物在SLRL试验中的反应完成分类后,根据Griesemer和Cueto(1980年)的列表对化合物的致癌反应进行分类。有62种化合物在致癌性和致突变性方面都可被分类为阳性或阴性。在这62种化合物中,致癌性和致突变性分类之间有56种(50种阳性和6种阴性)是一致的,或者说仅通过SLRL试验就有90%的化合物在致癌性方面能被正确分类。由于样本量不足,根据工作组制定的统计标准,有177种化合物无法被分类为阳性或阴性。大量测试不充分的化合物反映出许多实验并非为筛选而进行这一事实。对于样本量不足的化合物,还需要进一步开展工作。(摘要截取自400词)