首页> 外文期刊>The Journal of toxicological sciences >Collaborative work on evaluation of ovarian toxicity9) Effects of 2- or 4-week repeated dose studies and fertilitystudy of di(2-ethylhexyl)adipate (DEHA) in female rats
【24h】

Collaborative work on evaluation of ovarian toxicity9) Effects of 2- or 4-week repeated dose studies and fertilitystudy of di(2-ethylhexyl)adipate (DEHA) in female rats

机译:评估卵巢毒性的合作研究9)雌性大鼠2或4周重复剂量研究的效果和己二酸二(2-乙基己基)酯(DEHA)的生育力研究

获取原文
获取原文并翻译 | 示例
           

摘要

The present study was designed to confirm whether or not the ovarian toxicity of di(2-ethylhexyl)adipate (DEHA), which is known to have effects on female fertility, could be evaluated by the new method of histopathological examination of the ovaries in repeated dose toxicity. DEHA was orally administered to Crl:CD(SD) female rats at the doses of 0, 200, 1,000 and 2,000 mg/kg for 2 or 4 weeks in repeated dose toxicity study and for 2 weeks before mating, throughout mating and until Gestation Days 7 in female fertility. In the repeated dose toxicity studies, increase in atresia of large follicle, decrease in currently formed corpus luteum and follicular cyst were observed in the 1,000 mg/kg and above groups, suggesting that DEHA disturbed ovulation and large follicle growth. In the fertility study, a significant increase in mean estrus cycle length and post-implantation loss rate were observed in the 1,000 mg/kg and above groups, and a significant decrease in implantation rate and number of live embryos and a significant increase in pre-implantation loss rate were observed in the 2,000 mg/kg group. The histopathological changes of ovary observed in the repeated dose toxicity studies were correlated with the result that DEHA affected the estrus cycle in the female fertility study. In conclusion, a 2-week administration period is sufficient for detection of the ovarian toxicities following treatment with DEHA by new histopathological examination of the ovaries.
机译:本研究旨在确定是否可以通过反复进行卵巢组织病理学检查的新方法评估已知对女性生育力有影响的己二酸二(2-乙基己基)己二酸酯(DEHA)的卵巢毒性。剂量毒性。在重复剂量毒性研究中,以0、200、1,000和2,000 mg / kg的剂量向Crl:CD(SD)雌性大鼠口服DEHA持续2或4周,交配前,整个交配直至妊娠第2天女性生育能力7。在反复剂量毒性研究中,在1,000 mg / kg及以上的组中观察到大卵泡闭锁增加,当前形成的黄体和卵泡囊肿减少,这表明DEHA干扰了排卵和大卵泡生长。在生育力研究中,在1,000 mg / kg及以上的组中,平均发情周期长度和着床后损失率显着增加,而着床率和活胚胎数则显着下降,而前期胚胎的显着增加。在2000mg / kg组中观察到植入损失率。在重复剂量毒性研究中观察到的卵巢组织病理学变化与女性生殖力研究中DEHA影响发情周期的结果相关。总之,为期2周的给药期足以通过新的卵巢组织病理学检查来检测DEHA治疗后的卵巢毒性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号