FSH, oxytocin and IGF-I regulate the expression of sirtuin 1 in porcine ovarian granulosa cells
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
32469232
PubMed Central
PMC8648316
DOI
10.33549/physiolres.934424
PII: 934424
Knihovny.cz E-resources
- MeSH
- Apoptosis drug effects MeSH
- Granulosa Cells cytology drug effects metabolism MeSH
- Follicle Stimulating Hormone pharmacology MeSH
- Insulin-Like Growth Factor I pharmacology MeSH
- Cells, Cultured MeSH
- Ovary cytology drug effects metabolism MeSH
- Oxytocin pharmacology MeSH
- Swine MeSH
- Cell Proliferation drug effects MeSH
- Sirtuin 1 biosynthesis genetics metabolism MeSH
- Oxytocics pharmacology MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Follicle Stimulating Hormone MeSH
- Insulin-Like Growth Factor I MeSH
- Oxytocin MeSH
- Sirtuin 1 MeSH
- Oxytocics MeSH
The involvement of the mTOR system/enzyme sirtuin 1 (SIRT1) intracellular signaling system in the control of ovarian functions and its role in mediating hormonal action on the ovary has been proposed, but this hypothesis should be supported by a demonstrated influence of hormones on mTOR/SIRT1. Therefore, the aim of our in vitro experiments was to examine the effect of the known hormonal regulators of ovarian functions, such as follicle-stimulating hormone (FSH), oxytocin (OT) and insulin-like growth factor I (IGF-I), on mTOR/SIRT1. The accumulation of SIRT1 in porcine ovarian granulosa cells cultured with and without these hormones (at doses of 1, 10 or 100 ng.ml-1) was evaluated using immunocytochemistry. It was observed that the addition of FSH (at 10 ng.ml-1 but not at 1 or 100 ng/ml) and OT (at all tested doses) increased the expression of SIRT1 in ovarian cells. In addition, 100 ng.ml-1, but not at 1 or 10 ng.ml-1, of IGF-I decreased SIRT1 accumulation. Our observations are the first demonstration that hormones can directly regulate the ovarian mTOR/SIRT1 system and that this system could mediate the action of hormonal regulators on the ovary.
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