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生殖细胞诱变剂阶梯项目检测综合报告

Synthesis report of the step project detection of germ cell mutagens.

作者信息

Adler I D, Anderson D, Benigni R, Ehling U H, Laehdetie J, Pacchierotti F, Russo A, Tates A D

机构信息

GSF-Institut für Säugetiergenetik Neuherberg, Oberschleissheim, Germany.

出版信息

Mutat Res. 1996 Jun 12;353(1-2):65-84. doi: 10.1016/0027-5107(95)00240-5.

Abstract

The project 'Detection of Germ Cell Mutagens' was designed with three major goals: (1) Detection and characterization of germ-cell mutagens; (2) standardization and validation of new germ-cell tests; and (3) development of a data base on germ-cell mutagenicity. All three goals were achieved. The classical germ-cell tests were applied to characterize the genetic effects of acrylamide (AA), 1,3-butadiene (BD), trophosphamide (TP) and urethane (UR). All but UR were found to cause heritable genetic damage. The experimental data obtained for AA and BD were the basis for genetic risk evaluations during the EC/US Workshop on Risk Assessment 'Human Genetic Risk from Exposure to Chemicals, Focusing on the Feasibility of the Parallelogram Approach'. Nine chemicals were employed to validate the spermatid micronucleus assay with mice and rats: AA, BD and its metabolites 1,2-epoxybutene-3 and 1,2:3,4-diepoxybutane, chlorambucil, mitomycin C, methylnitrosourea, TP and UR. The spermatid micronucleus test was combined with micronucleus tests in somatic cells such as bone marrow or peripheral blood erythrocytes, and splenocytes which allowed a comparison of effects in somatic and germinal cells. Improvements of the spermatid micronucleus test included BrdU-labelling of premeiotic S-phase for the determination of stage sensitivity and fluorescence in situ hybridization with pancentromeric DNA-probes to distinguish between clastogenic and aneugenic events. The results indicate that the spermatid micronucleus test with its improvements is an adequate procedure to detect germ-cell clastogenicity and to compare the activity of chemicals in different tissues and between species, i.e., rats and mice. Other germ cell methods under study were the flow cytometric measurement of testicular sperm DNA and the cytogenetic analysis of preimplantation embryos for chromosomal aberrations and micronuclei. The collection of a reliable germ-cell data base was accomplished through a critical evaluation of the literature and with the data obtained in the present project. Remarkable concordance between responses of germ cell tests to chemical mutagens was the most striking conclusion to be drawn from the present data base.

摘要

“生殖细胞诱变剂检测”项目设定了三个主要目标:(1)检测和鉴定生殖细胞诱变剂;(2)新生殖细胞检测方法的标准化和验证;(3)建立生殖细胞致突变性数据库。所有这三个目标均已实现。应用经典的生殖细胞检测方法来鉴定丙烯酰胺(AA)、1,3 - 丁二烯(BD)、曲磷酰胺(TP)和尿烷(UR)的遗传效应。除UR外,其他物质均被发现可导致可遗传的遗传损伤。为AA和BD获得的实验数据是欧洲共同体/美国“接触化学品对人类遗传风险评估研讨会:聚焦平行四边形方法的可行性”期间进行遗传风险评估的基础。使用九种化学物质对小鼠和大鼠的精子细胞微核试验进行验证:AA、BD及其代谢产物1,2 - 环氧丁烯 - 3和1,2:3,4 - 二环氧丁烷、苯丁酸氮芥、丝裂霉素C、甲基亚硝基脲、TP和UR。精子细胞微核试验与体细胞如骨髓或外周血红细胞以及脾细胞中的微核试验相结合,从而能够比较化学物质在体细胞和生殖细胞中的效应。精子细胞微核试验的改进包括对减数分裂前S期进行BrdU标记以确定阶段敏感性,以及使用全着丝粒DNA探针进行荧光原位杂交以区分断裂剂和非整倍体剂事件。结果表明,经过改进的精子细胞微核试验是检测生殖细胞断裂剂活性以及比较化学物质在不同组织和不同物种(即大鼠和小鼠)之间活性的合适方法。正在研究的其他生殖细胞方法包括对睾丸精子DNA进行流式细胞术测量以及对植入前胚胎进行染色体畸变和微核的细胞遗传学分析。通过对文献的严格评估以及本项目获得的数据,完成了可靠的生殖细胞数据库的收集。从当前数据库得出的最显著结论是生殖细胞检测对化学诱变剂的反应之间存在显著的一致性。

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