Locally produced angiotensin II induces ovulation by stimulating prostaglandin production in in vitro perfused rabbit ovaries
| Autor: | Masao Akiba, M Karube, Takahisa Oda, N Koyama, Shigetatsu Shiokawa, Yasunori Yoshimura, Yukio Nakamura, Akari Yoshinaga |
|---|---|
| Rok vydání: | 1993 |
| Předmět: |
Ovulation
medicine.medical_specialty media_common.quotation_subject Indomethacin Prostaglandin Ovary Biology Dinoprost Chorionic Gonadotropin Dinoprostone chemistry.chemical_compound Endocrinology Internal medicine Renin–angiotensin system Follicular phase medicine Animals Progesterone media_common Dose-Response Relationship Drug Estradiol Angiotensin II Perfusion medicine.anatomical_structure chemistry Eicosanoid Female Rabbits Saralasin hormones hormone substitutes and hormone antagonists |
| Zdroj: | Endocrinology. 133:1609-1616 |
| ISSN: | 1945-7170 0013-7227 |
| DOI: | 10.1210/endo.133.4.8404601 |
| Popis: | The present study was undertaken to investigate the role of exogenous and endogenous angiotensin II (Ang II) in ovarian steroidogenesis and production of prostaglandin (PG) in in vitro perfused rabbit ovaries. The addition of 100 or 10 micrograms Ang II at 2-h intervals to the perfusate did not stimulate progesterone production, but significantly stimulated estradiol (E2) production by perfused rabbit ovaries. When the specific antagonist of Ang II, saralasin at 2 x 10(-6) M, was added to the perfusate 30 min before the onset of Ang II administration, Ang II-stimulated production of E2 was significantly blocked. Ang II also significantly stimulated both PGE2 and PGF2 alpha production, while the addition of saralasin to the perfusate significantly inhibited the Ang II-stimulated production of PG. The levels of PGs in ovaries perfused with saralasin plus 100 micrograms Ang II did not differ significantly from those in control ovaries perfused with medium alone. Exposure to human CG (hCG) significantly stimulated production of progesterone and E2 by perfused rabbit ovaries, while the concomitant administration of 2 x 10(-6) M saralasin significantly reduced only E2 production. Addition of saralasin to the perfusate inhibited hCG-stimulated PG production in a dose-dependent manner. The ovulatory efficiency in ovaries treated with hCG alone or hCG plus saralasin was significantly correlated with PG production by perfused rabbit ovaries at 12 h after exposure to hCG. The production of PG stimulated by Ang II was completely reduced by indomethacin treatment during the entire perfusion period. Indomethacin completely blocked Ang II-induced ovulation, but not Ang II-stimulated oocyte maturation. Concurrent administration of staurosporine, a protein kinase C inhibitor, at 10(-6) M significantly inhibited Ang II-stimulated meiotic maturation of ovulated ova and follicular oocytes. In conclusion, these results indicate that Ang II has a direct role in ovarian production of E2 and PG. An intrinsic renin-angiotensin system in the rabbit ovary may act as an intermediary of gonadotropin-stimulated PG production. Locally produced Ang II may induce ovulation in the rabbit ovary, at least in part, by stimulating PG production. |
| Databáze: | OpenAIRE |
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