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dc.contributor.authorSakin, Önder
dc.contributor.authorOruç, Muhammet Ali
dc.contributor.authorAnğin, Ali Doğukan
dc.contributor.authorAlan, Yasemin
dc.contributor.authorGökkaya, Mustafa
dc.contributor.authorSağdıç, Hasan
dc.contributor.authorMat, Emre
dc.contributor.authorBaşak, Kayhan
dc.contributor.authorAlan, Murat
dc.date.accessioned2025-01-15T12:14:31Z
dc.date.available2025-01-15T12:14:31Z
dc.date.issued2020en_US
dc.identifier.citationSakin, Ö., Oruç, M. A., Anğın, A. D., Alan, Y., Gökkaya, M., Sağdıç, H., ... & Alan, M. (2020). Can dehydroepiandosterone prevent chemotherapy-related damage? Investigation of protective effects of dehydroepiandosterone against paclitaxel-induced toxicity damage in rat ovaries. Journal of Experimental and Clinical Medicine, 37(3), 97-103.en_US
dc.identifier.urihttps://10.5835/jecm.omu.37.03.006
dc.identifier.urihttps://hdl.handle.net/20.500.12513/7045
dc.description.abstractOur aim is to evaluate whether dehydroepiandosterone has a protective effect on paclitaxel-induced ovarian damage. Group 1 (the control group): No treatment was administered. Intact ovarian tissue was removed and blood samples were taken for anti-mullerian hormone (AMH) test. Group 2 (the paclitaxel group): Rats received paclitaxel intraperitoneally at a single dose of 7.5 mg/kg. Group 3 (the paclitaxel + DHEA group): Rats received paclitaxel intraperitoneally at a single dose of 7.5 mg / kg at baseline and DHEA subcutaneously for 10 days at a dose of 60 mg / kg daily. Rats in groups 2 and 3 were sacrificed at the end of 10 days, ovarian tissues were removed and blood samples were taken for AMH test. The edema score was higher in the paclitaxel+DHEA group than in the normal group. Vasculary congestion score was higher in the paclitaxel and paclitaxel+DHEA groups than in the normal group. Cellular degeneration score was higher in paclitaxel group than normal group. Total score was higher in the paclitaxel and paclitaxel+DHEA groups than in the normal group. In the paclitaxel group, the number of tertiary follicles and ovarian volume were lower than in the normal group. Primordial follicles, secondary follicles, tertiary follicles, AMH level and ovarian volume of paclitaxel+DHEA group were lower than normal group. In conclusion DHEA was found to increase damage in paclitaxel-treated rats, leading to a decrease in follicle counts and AMH.en_US
dc.language.isoengen_US
dc.publisherOndokuz Mayis Universitesien_US
dc.relation.isversionof10.5835/jecm.omu.37.03.006en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnti-mullerian Hormoneen_US
dc.subjectDehydroepiandrosteroneen_US
dc.subjectOvaryen_US
dc.subjectPaclitaxelen_US
dc.subjectRaten_US
dc.titleCan Dehydroepiandosterone Prevent Chemotherapy-Related Damage? Investigation of Protective Effects of Dehydroepiandosterone Against Paclitaxel-İnduced Toxicity Damage İn Rat Ovariesen_US
dc.typeletteren_US
dc.relation.journalJournal of Experimental and Clinical Medicine (Turkey)en_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorIDMuhammet Ali Oruç / 0000-0002-4320-8579en_US
dc.identifier.volume37en_US
dc.identifier.issue3en_US
dc.identifier.startpage97en_US
dc.identifier.endpage103en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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