O'Neill C
Human Reproduction Unit, Royal North Shore Hospital of Sydney, St Leonards, NSW, Australia.
Reprod Fertil Dev. 1995;7(1):51-7. doi: 10.1071/rd9950051.
The effects of a number of platelet-activating factor (PAF)-antagonists on embryo implantation were investigated. Mice were treated from Day 1 to Day 4 of pregnancy with three defined PAF-antagonists: SRI 63 441, BN 52021, and WEB 2086. Necroscopies were performed on Day 8 and the number of implantation sites, the implantation rate (number of implanted embryos compared with the number of corpora lutea) and the proportion of animals pregnant were determined. Each agent caused a reduction in the number of implantation sites at relatively low doses. The dose that had a maximum contragestational effect was 40 micrograms, 10 micrograms and 10 micrograms (per 30 g bodyweight per day) for SRI 63 441, WEB 2086 and BN 52021 respectively. This contragestational effect was completely lost at twice (SRI 63 441), five times (WEB 2086) and ten times (BN 52021) the most effective dose. Treatment with WEB 2086 on the day of implantation (Day 4) by intraperitoneal injection or instillation into the uterus only did not significantly reduce the implantation rate and neither did treatment after implantation (Days 5-8). The results show that the pharmacology of PAF-antagonists in early pregnancy is not simple. An understanding of the actions of these agents in early pregnancy will require a detailed knowledge of their pharmacokinetics, pharmacodynamics and targets of action in early pregnancy.
研究了多种血小板激活因子(PAF)拮抗剂对胚胎着床的影响。在妊娠第1天至第4天,用三种特定的PAF拮抗剂(SRI 63 441、BN 52021和WEB 2086)对小鼠进行处理。在第8天进行尸检,确定着床部位的数量、着床率(着床胚胎数量与黄体数量之比)以及怀孕动物的比例。每种药物在相对低剂量时都会使着床部位的数量减少。对SRI 63 441、WEB 2086和BN 52021而言,产生最大抗孕作用的剂量分别为40微克、10微克和10微克(每日每30克体重)。这种抗孕作用在最有效剂量的两倍(SRI 63 441)、五倍(WEB 2086)和十倍(BN 52021)时完全消失。在着床日(第4天)通过腹腔注射或仅向子宫内滴注WEB 2086进行处理,并未显著降低着床率,着床后(第5 - 8天)进行处理也未降低着床率。结果表明,PAF拮抗剂在妊娠早期的药理学情况并不简单。要了解这些药物在妊娠早期的作用,需要详细了解它们的药代动力学、药效学以及在妊娠早期的作用靶点。