Activity of Ovarian Nitric Oxide Synthase (NOs) during Ovulatory Process in the Rat: Relationship with Prostaglandins (PGs) Production

• Published in: Nitric oxide 1999-08, Vol.3 (4), p.340-347
• Main Authors: Faletti, Alicia, Pérez Martı́nez, Silvina, Perotti, Christian, de Gimeno, Martha A.F.
• Format: Article
• Language: English
• Subjects: Animals; Chorionic Gonadotropin - pharmacology; Dinoprost - biosynthesis; Enzyme Activation; Enzyme Inhibitors - pharmacology; Female; Gonadotropins, Equine - pharmacology; Molsidomine - analogs & derivatives; Molsidomine - pharmacology; NG-Nitroarginine Methyl Ester - pharmacology; Nitric Oxide - physiology; Nitric Oxide Donors - pharmacology; Nitric Oxide Synthase - antagonists & inhibitors; Nitric Oxide Synthase - physiology; Nitric Oxide Synthase Type II; Nitric Oxide Synthase Type III; NOs activity; omega-N-Methylarginine - pharmacology; ovary; Ovary - enzymology; Ovulation - physiology; Ovulation Induction; PGs production; Prostaglandin-Endoperoxide Synthases - metabolism; Prostaglandins E - biosynthesis; rat ovulation; Rats; Rats, Wistar
• ISSN: 1089-8603; 1089-8611
• DOI: 10.1006/niox.1999.0231

Nitric oxide (NO) is synthesized by the rat ovary and a role in the follicular development, the ovulation, and the luteal formation has been postulated. The aims this study were to determine the activity of nitric oxide synthase (NOs) enzyme during the ovulatory process and to demonstrate the existence of a relationship between the ovarian NO production and the synthesis of prostaglandins (PGs) involved in the follicular rupture. Prepuberal rats treated with PMSG/hCG to induce ovulation were used. The NOs activity, measured by [14C]citrulline formation, showed an increase after PMSG administration and reached a maximum at 10 h after hCG injection. NOs activity remained high up to 24 h post ovulation. At 10 h after the hCG injection, the activity of Ca2+-dependent NOs (constitutive NOs) was similar to that seen at 0 h, and the activity of Ca2+-independent NOs (inducible NOs) increased from 14.4 to 51% of total activity. The in vitro ovarian production of PGE and PGF2α was inhibited by L-NAME and stimulated by 3-morpho-linosydnonimine (SIN-1), a NO donor. The in vivo production of ovarian prostaglandins was also inhibited by the intrabursal administration of two NOs inhibitors, NG-nitro-l-arginine methyl ester (L-NAME) and NG-monomethyl-l-arginine (L-NMMA). Our results suggest that the inducible NOs (iNOs) is the main isoform involved in the ovulatory process and that the NO produced stimulates the synthesis of both PGE and PGF2α from the cyclooxygenase pathway, to enhance the process of follicle rupture.