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检测化学物质对中国仓鼠精原细胞诱变作用的方法:环磷酰胺、糖精和甜蜜素的实验结果

Method for testing mutagenic effects of chemicals on spermatogonia of the Chinese hamster: results obtained with cyclophosphamide, saccharin, and cyclamate.

作者信息

Machemer L, Lorke D

出版信息

Arzneimittelforschung. 1975;25(12):1889-96.

PMID:1243659
Abstract

The action of different cyclophosphamide doses on spermatogonia of the Chinese hamster was examined. Two oral treatments at an interval of 24 h were carried out and spermatogonia were prepared for examination 24 or 48 h after the second dose. Accordingly the effects of 5 oral cyclophosphamide doses given on five consecutive days were tested on spermatogonia and preparations were made 24 or 72 h after the last treatment. The results so obtained form the basis of reference for findings following oral administration of saccharin sodium, sodium cyclamate, or trimethylphosphate. Male Chinese hamsters, 6-8 per group, were used, from each of which about 100 metaphases were evaluated. Preparation was carried out essentially according to Hoo and Bowles [Mutation Res. 13, 85-88 (1971)]. gaps, breaks, fragments, deletions and translocations were rated as structural aberrations. For every dose and every time of preparation the incidence of metaphases with aberrations, with or without gaps, and with translocations were assessed. The different experiments led to the following conclusions: 1. By analysis of spermatogonial metaphases of treated Chinese hamsters chemically induced chromosome aberrations can be proved with certainty. 2. Incidence of metaphases with translocations is a sensitive measure which is distinctly superior to the summary determination of all aberrations. In this way it was possible to show a mutagenic influence of 2 times 8 mg/kg cyclophosphamide p.o. 3. Following two cyclophosphamide doses administered at an interval of 24 h it was found that preparations of spermatogonia 48 h after the second dose was better suited for the evaluation than that at 24 h, for aberrations were more frequent with the same treatment. After five cyclophosphamide treatments at 24-h intervals, aberrations were somewhat more frequent 24 h after the last dose than at 72 h; in any case the values exceeded significantly the results of untreated controls. 4. A conclusive numeric chromosome analysis is not possible with the spermatogonia test, since a relatively high percentage of non-diploid cells is apparently of methodological origin. 5. Tests with 2 times 500 or 5 times 1000 mg/kg trimethylphosphate orally showed an increase in chromosome aberrations compared with controls indicating mutagenic effects in both cases; with 5 times 1000 mg/kg p.o., however, the figures were low as a result of marked mitotic inhibition. 6. The results of the spermatogonia test on Chinese hamsters revealed no mutagenic effects of saccharin sodium 2 times 5000 mg/kg orally, and of sodium cyclamate 5 times 2000 mg/kg orally. This is based on comparisons of the results both with untreated controls and positive controls treated with trimethylphosphate or cyclophosphamide.

摘要

研究了不同剂量环磷酰胺对中国仓鼠精原细胞的作用。进行了两次口服给药,间隔24小时,并在第二次给药后24或48小时制备精原细胞用于检查。相应地,测试了连续五天给予的5次口服环磷酰胺剂量对精原细胞的影响,并在最后一次治疗后24或72小时制备样本。所获得的结果为口服糖精钠、甜蜜素或磷酸三甲酯后的研究结果提供了参考依据。每组使用6 - 8只雄性中国仓鼠,每组评估约100个中期相。样本制备基本上按照胡和鲍尔斯[《突变研究》13, 85 - 88(1971)]的方法进行。裂隙、断裂、片段、缺失和易位被评定为结构畸变。对于每个剂量和每次样本制备时间,评估有畸变、有或无裂隙以及有易位的中期相的发生率。不同的实验得出以下结论:1. 通过对经处理的中国仓鼠精原细胞中期相的分析,可以确切证明化学诱导的染色体畸变。2. 有易位的中期相发生率是一种敏感指标,明显优于对所有畸变的综合测定。通过这种方式,有可能显示出2次口服8 mg/kg环磷酰胺的诱变作用。3. 在间隔24小时给予两次环磷酰胺剂量后,发现第二次给药后48小时制备的精原细胞样本比24小时制备的样本更适合评估,因为相同处理下畸变更频繁。在间隔24小时进行5次环磷酰胺处理后,最后一次给药后24小时的畸变比72小时略多;无论如何,这些值显著超过未处理对照组的结果。4. 精原细胞试验无法进行确凿的数字染色体分析,因为相对较高比例的非二倍体细胞显然是方法学原因导致的。5. 口服2次500或5次1000 mg/kg磷酸三甲酯的试验表明,与对照组相比染色体畸变增加,表明两种情况下都有诱变作用;然而,口服5次1000 mg/kg时,由于明显的有丝分裂抑制,数值较低。6. 对中国仓鼠的精原细胞试验结果显示,口服2次5000 mg/kg糖精钠和5次2000 mg/kg甜蜜素没有诱变作用。这是基于与未处理对照组以及用磷酸三甲酯或环磷酰胺处理的阳性对照组的结果比较得出的。

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引用本文的文献

1
Effects on mouse embryos of in utero exposure to saccharin: teratogenic and chromosome effects.子宫内暴露于糖精对小鼠胚胎的影响:致畸和染色体效应。
Arch Toxicol. 1985 Feb;56(4):283-7. doi: 10.1007/BF00295169.
2
The effect of cyclophosphamide on the centromere separation sequence in Chinese hamster spermatogonia.环磷酰胺对中国仓鼠精原细胞着丝粒分离序列的影响。
Hum Genet. 1977 Dec 23;39(3):359-62. doi: 10.1007/BF00295432.
3
Mutagenicity studies with praziquantel, a new anthelmintic drug, in mammalian systems.
Arch Toxicol. 1978 Jan 25;39(3):187-97. doi: 10.1007/BF00368227.
4
Cyto-enetic investigations of mammals. Comparison of the genetic activity of cytostatics in mammals.
Arch Toxicol. 1977 Sep 21;38(1-2):35-43. doi: 10.1007/BF00293661.
5
Mutagenicity testing in industry.工业中的致突变性测试。
Arch Toxicol. 1977 Sep 21;38(1-2):235-40. doi: 10.1007/BF00293670.