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Biology of Reproduction, Vol 17, 58-63, Copyright © 1977 by Society for the Study of Reproduction
1 Department of Obstetrics and Gynecology,
Pennsylvania Hospital and the University of Pennsylvania School of Medicine,
Philadelphia, Pennsylvania 19107 Ovulation has been achieved in vitro in the isolated perfused rabbit ovary. The ovarian artery
was cannulated 8 h after HCG administration and the ovary perfused and removed for in vitro
study. The effects on ovulation of the addition of PGE2, and PGF2
, indomethacin and HCG to
the perfusate were studied. Ovulation occurred in 8 of 12 perfused ovaries in the control group (no
drug), 7 of 12 in the group perfused with supplementary HCG (1 IU/ml), 11 of 12 with PGF2
(1
µg/ml), 3 of 12 with PGE2 (1 µg/ml) and 2 of 12 with indomethacin (0.5 µg/ml). Ovulation always
occurred in the contralateral ovary which remained in situ as an in vivo control. Addition of
indomethacin to the perfusate reduced the incidence of ovulation in vitro when compared to the
control group (P<0.01). Ovulation was also reduced (P<0.01) when the ovaries treated with PGE2
were compared to the control, and when PGE2 was compared to PGF2
(P<0.005). These
observations indicate that the presence of PGF2
within the ovary may be essential to the process
of ovulation. The inhibitory effects of indomethacin and PGE2 on ovulation in the perfused in
vitro rabbit ovary parallel previous observations in the intact HCG-treated rabbit. The use of the
perfused preparation provides additional evidence that the inhibitory effects of indomethacin and
PGE2 on ovulation are mediated at the ovarian level. Simultaneous recordings of ovarian
contractions were carried out and no association could be established between contractile pattern,
ovulation or number of ovulation points.
Note:
ACKNOWLEDGMENTS
This investigation was supported by National Institutes of Health Grant HD-05948 and in part by the
Mitchell and Lillian Duberstein Foundation. We thank
Clement A. Stone, Ph.D. of Merck, Sharp and Dohme,
West Point, Pennsylvania, for the supply of indomethacin and John E. Pike, D.Ph. of the Upjohn Company, Kalamazoo, Michigan for the prostaglandins.
The authors also thank Thomas J. Henry, Judy L.
Reitman, Judith Rosenthal and Carol Pitman for their
excellent technical assistance. Statistical evaluations
were carried out with the assistance of Michael Lee of
the University of Pennsylvania Medical School Computer Facility.
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