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氯化甲烷诱导Fischer 344大鼠着床前丢失的原因之一:受精失败

Failure of fertilization as a cause of preimplantation loss induced by methyl chloride in Fischer 344 rats.

作者信息

Working P K, Bus J S

出版信息

Toxicol Appl Pharmacol. 1986 Oct;86(1):124-30. doi: 10.1016/0041-008x(86)90405-9.

Abstract

Methyl chloride (MeCl) is a testicular and epididymal toxicant in the Fischer 344 rat that induces significant decreases in sperm quality in males and significant increases in preimplantation embryonic loss in females mated to exposed males. This study examined the possibility that these losses are due to failure of fertilization and not to preimplantation embryonic death. Groups of males either were exposed to 1000 or 3000 ppm MeCl 6 hr/day for 5 days or received a single ip injection of 0.2 mg/kg triethylenemelamine (TEM) on Day 5 and were bred to two females weekly for up to 8 weeks. Females were killed 12 hr postmating; embryos and ova were isolated and scored as fertilized or unfertilized. Nearly 90% (602/683) of the normal ova recovered from females bred to control males were fertilized, and fertilization rates in the 1000-ppm MeCl and TEM groups were not significantly depressed from that level. The percentage of fertilized ova in the 3000-ppm MeCl group was significantly decreased, ranging from 3 to 72% over the 8 weeks. The frequency of unfertilized ova in this group always equaled or exceeded the frequency of preimplantation loss recorded in an earlier dominant lethal assay. In contrast, only a fraction of the preimplantation losses caused by the genotoxicant TEM could be accounted for by failure of fertilization. After culture of fertilized ova for 24 hr, only the TEM group exhibited a significant decrease in the number of fertilized ova which cleaved (85 vs 96% in the control). We conclude that the preimplantation loss caused by MeCl exposure is due to failure of fertilization and not to a genotoxic effect of MeCl. The methods used here permit a more accurate assessment of the reproductive toxicity of a chemical by discriminating between its cytotoxic and genotoxic effects.

摘要

甲基氯(MeCl)是一种对费希尔344大鼠睾丸和附睾有毒性的物质,可导致雄性大鼠精子质量显著下降,与暴露雄性大鼠交配的雌性大鼠着床前胚胎损失显著增加。本研究探讨了这些损失是由于受精失败而非着床前胚胎死亡的可能性。将雄性大鼠分为几组,一组每天6小时暴露于1000或3000 ppm的MeCl中,持续5天;另一组在第5天单次腹腔注射0.2 mg/kg的三亚乙基三聚氰胺(TEM),然后每周与两只雌性大鼠交配,持续8周。交配后12小时处死雌性大鼠;分离胚胎和卵子,并将其分为已受精或未受精。从与对照雄性大鼠交配的雌性大鼠中回收的正常卵子,近90%(602/683)已受精,1000 ppm MeCl组和TEM组的受精率与该水平相比无显著降低。3000 ppm MeCl组的受精卵百分比显著下降,在8周内从3%到72%不等。该组未受精卵的频率始终等于或超过早期显性致死试验中记录的着床前损失频率。相比之下,由基因毒性物质TEM引起的着床前损失中,只有一小部分可归因于受精失败。将受精卵培养24小时后,只有TEM组出现受精卵分裂数量显著减少(对照组为96%,TEM组为85%)。我们得出结论,MeCl暴露引起的着床前损失是由于受精失败,而非MeCl的基因毒性作用。此处使用的方法通过区分化学物质的细胞毒性和基因毒性作用,能够更准确地评估其生殖毒性。

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