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dc.contributor.advisorFattahi, Amir
dc.contributor.advisorHamadi, Kobra
dc.contributor.authorNikanfar, Saba
dc.date.accessioned2022-02-20T07:37:40Z
dc.date.available2022-02-20T07:37:40Z
dc.date.issued2021en_US
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/66149
dc.description.abstractThe involvement of Oncostatin M (OSM), a recently identified adipokine, in ovarian function is unknown. Therefore, we investigated the association of OSM signaling pathway with ovarian functions and PCOS pathogenesis. Materials and Methods: In the in-vivo experiment, 30 PCOS and 30 healthy women who underwent the ICSI procedure were enrolled. The lipid, carbohydrate, and hormonal profiles, as well as OSM and OSMR levels, were evaluated in the follicular fluid (FF). Moreover, the expression of insulin receptor substrates (IRS1 and IRS2), OSM, OSMR, suppressor of cytokine signaling 3 (SOCS3), and androgen receptor (AR) genes were analyzed in the isolated cumulus cells (CCs) and also after treatment with recombinant OSM. Results: Follicular concentrations of OSM and OSMR were significantly lower in PCOS compared to control women (p<0.001) and were positively correlated with the oocyte maturation and fertilization rates in the PCOS group. Furthermore, the SOCS3 expression was upregulated in PCOS patients compared to the controls (p=0.043). The treatment of cells with recombinant OSM significantly increased SOCS3, OSMR, IRS-1, and -2 expression and decreased AR expression.en_US
dc.language.isofaen_US
dc.publisherTabriz University of Medical Sciences, Faculty of Medicineen_US
dc.relation.isversionofhttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/66148en_US
dc.subjectFollicular fluiden_US
dc.subjectOncostatin Men_US
dc.subjectOocyte maturationen_US
dc.subjectPolycystic ovary syndromeen_US
dc.titleThe study of the levels of oncostatin M and its receptor in granulosa cells and follicular fluid of women with polycystic ovarian syndrome and investigation of human recombinant oncostatin M effects on granulosa cells in vitroen_US
dc.typeThesisen_US
dc.contributor.supervisorNouri, Mohammad
dc.contributor.supervisorSamadi, Naser
dc.identifier.docno6010258en_US
dc.identifier.callno10258en_US
dc.description.disciplineClinical Biochemistryen_US
dc.description.degreePh. Den_US


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