Inhibitors of platelet activation,
alprazolam,
iloprost and
SRI 63-441, were used to demonstrate the necessity of embryo-derived
platelet-activating factor (PAF) activity for the establishment of pregnancy in mice. In a splenectomized mouse bioassay 6 micrograms
alprazolam inhibited, for 3 h, the
thrombocytopenia induced by 0.1 micrograms PAF; 4 micrograms
iloprost and 0.5 microgram
SRI 63-441 were effective for 6 and 12h respectively. The administration of 2 micrograms
iloprost/30 g
body weight on Days 1 and 4 of pregnancy and twice daily on Days 2 and 3 caused a 50% reduction (P less than 0.0005) in the number of implantation sites in the uterus at Day 8 of pregnancy, without affecting (P greater than 0.05) the number of corpora lutea. A similar reduction in the number of implantation sites was achieved with 20 micrograms
SRI 63-441/30 g
body weight/day. The reduction in implantation rate was evident on Day 5 of pregnancy by visualizing the implantation sites with
pontamine sky blue.
SRI 63-441 had no effect on peripheral blood
progesterone concentrations from Day 1 to Day 9 of pregnancy, and did not appear to inhibit implantation by blocking the preimplantation surge of
oestradiol. The number and morphology of blastocysts flushed from the uterus of Day 4 inhibitor-treated mice was not different (P greater than 0.05) from the controls. The cleavage rate and morphology of embryos cultured from the 2-cell to blastocyst stage in media containing
SRI 63-441 or
iloprost (10 micrograms/ml) were normal, precluding a gross toxic effect. Simultaneous administration of 1 microgram
PAF-acether to treated animals re-established pregnancy rates to levels not significantly different (P greater than 0.05) from the controls.