首页> 外文期刊>Reproductive and Developmental Medicine >Safety of mifepristone in medical abortion in hyperthyroidism pregnant mice
【24h】

Safety of mifepristone in medical abortion in hyperthyroidism pregnant mice

机译:米非司酮在甲状腺功能亢进妊娠小鼠药物流产中的安全性

获取原文
获取外文期刊封面目录资料

摘要

Objective: To study the safety of mifepristone on thyroid hormone level by using hyperthyroidism pregnant model in mouse to simulate the process of medical abortion and observe the changes of thyroid hormone during abortion. Methods: A total of 60 female Institute of Cancer Research (ICR) mice aged 6–8 weeks were divided into control group, control group with 0 mgRU486 group (control-0 mgRU486), control group with 2 mgRU486 group (control-2 mgRU486), hyperthyroid pregnant mice with 0 mgRU486 group (hyper-0 mgRU486), hyperthyroid pregnant mice with 2 mgRU486 group (hyper-2 mgRU486), and hyperthyroid pregnant mice with 20 mgRU486 group (hyper-20 mgRU486). In the hyperthyroidism groups, L-thyroxine sodium was intraperitoneally injected every day at 30 μg·kgsup?1/sup·daysup?1/sup until the end of the experiment. On the 7supth/sup day of the experiment, free triiodothyronine (FT3), free tetraiodothyroxine (FT4), thyroxine (TT4), and thyroid-stimulating hormone (TSH) levels were tested. The mice in the control groups and those in the experimental groups were paired with the male mice (2:1) on the 10supth/sup day of the experiment, and the caging was recorded. On the 8supth/sup day of pregnancy (day 8), pregnant mice were subcutaneously injected with mifepristone in different doses and were sacrificed 6 h later. Pregnancy rate and the number of embryos were recorded. Thyroid tissues were observed by hematoxylin and eosin (HE) staining. Serum TSH level was determined by radioimmunoassay. Results: Six hours after injection with mifepristone, serum FT3, FT4, and TT4 levels of pregnant mice were all increased. The increased levels in the mice under hyperthyroidism were different from those in the control groups (P 0.05). There was no difference in the embryo number and pregnancy rate between the experimental and the control groups; HE staining indicated that there was no significant change in microscopic features before and after mifepristone administration. Conclusion: Serum thyroid hormone level of mice under hyperthyroidism was significantly increased after mifepristone administration. Therefore, mifepristone should be avoided when hyperthyroidism has not been controlled.
机译:目的:通过模拟甲状腺功能亢进小鼠模型,研究米非司酮对甲状腺激素水平的安全性,模拟药物流产过程,观察流产过程中甲状腺激素的变化。方法:将60只6-8周大的雌性癌症研究所(ICR)小鼠分为对照组,对照组(0 mgRU486组)(对照组:0 mgRU486),对照组(2 mgRU486组)(对照组:2 mgRU486)。 ),0 mgRU486组的甲状腺功能亢进的怀孕小鼠(-0 mgRU486超高),2 mgRU486组的甲状腺功能亢进的怀孕小鼠(-2 mgRU486超高)和20 mgRU486组的甲状腺功能亢进的怀孕小鼠(超20 mgRU486)。在甲状腺功能亢进组中,每天以30μg·kg ?1 ·天?1 腹膜内注射L-甲状腺素钠直至实验结束。在实验的第7天,测试了游离三碘甲状腺素(FT3),游离四碘甲状腺素(FT4),甲状腺素(TT4)和促甲状腺激素(TSH)的水平。在实验的第10天,将对照组和实验组的小鼠与雄性小鼠(2∶1)配对,并记录其笼养。在怀孕的第8天(第8天),皮下注射米非司酮以不同剂量皮下注射给怀孕的小鼠,并在6小时后处死。记录怀孕率和胚胎数。通过苏木精和曙红(HE)染色观察甲状腺组织。通过放射免疫测定法测定血清TSH水平。结果:米非司酮注射后6小时,妊娠小鼠的血清FT3,FT4和TT4水平均升高。甲状腺功能亢进症小鼠的升高水平与对照组相比有所不同(P <0.05)。实验组和对照组之间的胚胎数和受孕率没有差异。 HE染色表明,米非司酮给药前后的微观特征无明显变化。结论:米非司酮给药后甲状腺功能亢进症小鼠血清甲状腺激素水平明显升高。因此,当甲亢尚未得到控制时,应避免使用米非司酮。

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