Skip to main content
. 1999 Jun 15;13(12):1561–1574. doi: 10.1101/gad.13.12.1561

Table 1.

Implantation of wild-type blastocysts transferred into pseudopregnant wild-type or COX2−/− mice treated with various agonists

Genotype
Treatment
Day of sacrifice
No. of blastocysts transferred
No. of recipients
No. of mice with IS (%)
No. of mice without IS
No. of IS (%)
(+/+) vehicle 6 112 9 9 (100) 0 55 (49.1)
(+/+) 8 199 12 12 (100) 0 83 (41.7)
(−/−) vehicle 6 139 10 3 (30) 7a 7 (5)
(−/−) 8 120 10 3 (30) 7a 27 (22.5)
(−/−) cPGI 6 98 6 6 (100) 0 32 (32.7)
(−/−) 8 99 8 8 (100) 0 44 (44.4)
(−/−) cicaprost 6 64 4 0 (0) 4a 0 (0)
(−/−) L-165,041 8 107 7 7 (100) 0 43 (40.2)
(−/−) PGE2 6 98 6 4 (66.7) 2 16 (16.3)
(−/−) 8 57 5 3 (60) 2a 10 (17.5)
(−/−) L-165,041 + 9-cis-RA 6 95 8 8 (100) 0 59 (62.1)
(−/−) cPGI + PGE2 8 124 10 9 (90) 1 60 (48.4)
(−/−) L-165,041 + PGE2 8 80 6 5 (83.3) 1 36 (45)

Day 4 wild-type blastocysts were transferred into day 4 pseudopregnant uteri of wild-type or COX2−/− recipients. Mice were injected (ip) with the vehicle, cPGI, cicaprost, L-165,041, PGE2, L-165,041 plus 9-cis-RA, cPGI plus PGE2, or L-165,041 plus PGE2 at 1700 hr on the day of blastocyst transfers and each day thereafter until sacrificed. Recipients were examined for implantation sites (IS) on days 6 or 8 by the blue dye method. The doses of various agonists are described in Materials and Methods. Uteri from mice without IS were flushed with saline to recover unimplanted blastocysts. All COX2−/− recipients received progesterone (2 mg/mouse) from day 3 until sacrificed. 

a

A number of delayed blastocysts was recovered from uterine flushings