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Published on: May 11, 2017
Effects of nitric oxide synthase inhibitors on porcine oocyte meiotic maturation
Yong Tao1, Huirong Xie, Haiyan Hong
1College of Biological Sciences, China Agricultural University, Beijing and Anhui Agricultural University, Anhui, China.
Abstract:
As an important biological messenger, nitric oxide (NO) exhibits a wide range of effects during physiological and pathophysiological processes, including mammalian oocyte meiotic maturation. The present study investigated whether NO derived from two nitric oxide synthase (NOS) isoforms, inducible NOS (iNOS) or endothelial NOS (eNOS), is involved in the meiotic maturation of porcine oocytes. Meanwhile, the cumulus cells' function in meiotic maturation and their interaction with oocyte development and degeneration were also investigated using cumulus-enclosed oocytes (CEOs) and denuded oocytes (DOs). Different inhibitors for NOS were supplemented to the medium. Cumulus expansion, cumulus cell DNA fragmentation and oocyte meiotic resumption were evaluated 48 h after incubation. Aminoguanidine (AG), a selective inhibitor for iNOS, suppressed cumulus expansion and inhibited CEOs to resume meiosis (p < 0.05), but did not inhibit cumulus cell DNA fragmentation. Both Nomega-nitro-L-arginine (L-NNA) and Nomega-nitro-L-arginine methyl ester (L-NAME), inhibitors for both iNOS and eNOS, delayed cumulus expansion, inhibited cumulus cell DNA fragmentation and inhibited CEOs to resume meiosis. Such effects were not seen in DOs. These results indicate that iNOS-derived NO is necessary for cumulus expansion and meiotic maturation by mediating the function of the surrounding cumulus cells, and eNOS-derived NO is also involved in porcine meiotic maturation.
Insights
Nitric oxide (NO) from inducible nitric oxide synthase (iNOS) is crucial for porcine oocyte maturation and cumulus expansion. Endothelial NOS (eNOS) also plays a role in oocyte maturation.
Area of Science:
- Reproductive Biology
- Cell Signaling
- Biochemistry
Background:
- Nitric oxide (NO) is a key signaling molecule in various physiological and pathological processes.
- NO influences mammalian oocyte meiotic maturation.
- The roles of specific nitric oxide synthase (NOS) isoforms in porcine oocyte maturation require elucidation.
Purpose of the Study:
- To investigate the involvement of inducible NOS (iNOS) and endothelial NOS (eNOS) in porcine oocyte meiotic maturation.
- To examine the function of cumulus cells in oocyte development and degeneration.
- To differentiate the roles of iNOS and eNOS in oocyte maturation using specific inhibitors.
Main Methods:
- Porcine oocytes (cumulus-enclosed oocytes - CEOs and denuded oocytes - DOs) were cultured with NOS inhibitors.
- Cumulus expansion, cumulus cell DNA fragmentation, and oocyte meiotic resumption were assessed.
- Selective iNOS inhibitor (Aminoguanidine) and non-selective NOS inhibitors (L-NNA, L-NAME) were used.
Main Results:
- Selective iNOS inhibition (Aminoguanidine) suppressed cumulus expansion and oocyte meiotic resumption in CEOs.
- Non-selective NOS inhibition (L-NNA, L-NAME) delayed cumulus expansion, inhibited cumulus cell DNA fragmentation, and reduced meiotic resumption in CEOs.
- No significant effects of NOS inhibitors were observed in DOs.
Conclusions:
- iNOS-derived NO is essential for cumulus expansion and meiotic maturation, mediating cumulus cell function.
- eNOS-derived NO also contributes to porcine oocyte meiotic maturation.
- Cumulus cells play a critical role in oocyte maturation, influenced by NO signaling.
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