Mailhes J B, Preston R J, Lavappa K S
Mutat Res. 1986 Jan-Mar;167(1-2):139-48. doi: 10.1016/0165-1110(86)90014-x.
This paper presents an evaluation of and offers recommendations for assays to detect chemically induced aneuploidy in mammalian female germ cells. 72 papers on female germ cell aneuploidy, published from 1970 to 1984, were reviewed. 28 papers were selected for critical evaluation; the other 44 papers were rejected according to pre-established criteria. Salient points emerging from the information reviewed allow an assessment of the current status of mammalian female germ cell tests for aneuploidy. The majority of data have been obtained by analyzing metaphase II mouse oocyte chromosomes following superovulation. Various classes of chemicals were administered usually around the time of ovulation. Dose-response relationships have not been obtained for the majority of chemicals evaluated. The method of data reporting and analysis usually was not conducive to comparisons among different studies. Few of the 16 chemicals studied can be regarded as negative for their ability to induce aneuploidy, whereas an even smaller number should be considered as positive. Certainly, a need exists to identify the chemicals and the dosages that could increase the incidence of aneuploidy in mammalian female germ cells. Obtaining such data definitely is feasible in cytogenetic laboratories. However, the mammalian female germ cell aneuploid assay should not be perceived as a rapid, inexpensive, routine procedure. The assay is capable of detecting aneuploidy following anaphase I when metaphase II oocytes are studied and following anaphases I and II when first-cleavage zygotes are studied.
本文对检测哺乳动物雌性生殖细胞化学诱导非整倍体的分析方法进行了评估并给出了建议。回顾了1970年至1984年发表的72篇关于雌性生殖细胞非整倍体的论文。挑选了28篇进行严格评估;根据既定标准拒绝了其他44篇论文。从所回顾的信息中得出的要点有助于评估哺乳动物雌性生殖细胞非整倍体检测的现状。大多数数据是通过分析超排卵后中期II小鼠卵母细胞染色体获得的。通常在排卵前后给予各类化学物质。对于大多数评估的化学物质,尚未获得剂量反应关系。数据报告和分析方法通常不利于不同研究之间的比较。所研究的16种化学物质中,很少有能被视为诱导非整倍体能力阴性的,而应被视为阳性的化学物质数量更少。当然,有必要确定能够增加哺乳动物雌性生殖细胞非整倍体发生率的化学物质及其剂量。在细胞遗传学实验室获取此类数据肯定是可行的。然而,不应将哺乳动物雌性生殖细胞非整倍体检测视为一种快速、廉价的常规程序。当研究中期II卵母细胞时,该检测能够检测到后期I后的非整倍体;当研究第一次分裂合子时,能够检测到后期I和后期II后的非整倍体。