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BOR - Papers in Press, published online ahead of print April 30, 2003.
Biol Reprod 2003, 10.1095/biolreprod.102.010710
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BIOLOGY OF REPRODUCTION 69, 835–842 (2003)
DOI: 10.1095/biolreprod.102.010710
© 2003 by the Society for the Study of Reproduction, Inc.


Ovary

Possible Role of Cyclooxygenase II in the Acquisition of Ovarian Luteal Function in Rodents1

Toshihiro Sakurai3, Kazuhiro Tamura2,3, Shiki Okamoto4, Takahiko Hara4, and Hiroshi Kogo3

Department of Pharmacology,3 Tokyo University of Pharmacy and Life Science, Hachioji, Horinouchi, Tokyo 192-0392, Japan Tokyo Metropolitan Institute of Medical Science,4 Honkomagome, Bunkyo-ku, Tokyo 113-0032, Japan

The development of the corpus luteum (CL), which involves angiogenesis, is essential for the establishment of early pregnancy. We investigated the roles of the prostaglandin synthases cyclooxygenase (COX) I and COX-II in angiogenesis and progesterone production in the newly formed CL, using inhibitors of the COX enzymes and the gonadotropin-induced pseudopregnant rat as a model. Injection of indomethacin, a nonselective COX inhibitor, on the day of ovulation and the following day decreased serum levels of progesterone, as did injection of the selective COX-II inhibitor NS-398. In contrast, a selective COX-I inhibitor, SC-560, had no effect on serum progesterone concentrations. None of the inhibitors had any effect on the weight of the superovulated ovaries or on the synthesis of progesterone by cultured luteal cells. To determine whether changes in angiogenesis are responsible for the decrease in progesterone synthesis, we measured hemoglobin and CD34 levels in luteinized ovaries following injection of COX inhibitors and measured the relative frequency of cells positive for platelet-endothelial cell adhesion molecule as a specific marker for endothelial cells. All of these parameters were reduced by the COX-II inhibitors, suggesting that changes in the vasculature are responsible for the decrease in serum progesterone. Histological examination of ovarian corrosion casts indicated that NS-398 inhibited the establishment of luteal capillary vessels following the injection of hCG. The results are consistent with the hypothesis that the activity of COX-II is associated with the formation of functional CL via its stimulation of angiogenesis.

1 This work was partially supported by a Grant-in-Aid for Scientific Research from the Promotion and Mutual Aid Corporation for Private Schools of Japan.

2 Correspondence: Kazuhiro Tamura, Department of Pharmacology, Tokyo University of Pharmacy and Life Science, Hachioji, Horinouchi 1432-1, Tokyo 192-0392, Japan. FAX: 81 426 76 4529; hiro{at}ps.toyaku.ac.jp




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