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dc.contributor.authorSaat, Nevzat
dc.contributor.authorRişvanlı, Ali
dc.contributor.authorDoğan, Halef
dc.contributor.authorÖnalan, Ebru Etem
dc.contributor.authorAkpolat, Nusret
dc.contributor.authorŞeker, İbrahim
dc.contributor.authorŞahna, Engin
dc.date.accessioned2020-12-17T08:08:39Z
dc.date.available2020-12-17T08:08:39Z
dc.date.issued2019en_US
dc.identifier.urihttps://doi.org/10.1080/10520295.2019.1605456
dc.identifier.urihttps://hdl.handle.net/20.500.12462/10924
dc.descriptionSaat, Nevzat (Balikesir Author)en_US
dc.description.abstractWe investigated the use of melatonin to improve fertility and reduce uterine damage caused by torsion of the uterus in pregnant rats. We used 35 pregnant rats at gestational age 18 days. The animals were randomized into five groups. Group 1 was anesthetized only. Group 2 was subjected to experimental uterine torsion of 360 degrees and the torsion was corrected after 6 h. Group 3 was subjected to uterine torsion of 360 degrees, the torsion was corrected after 6 h and melatonin was administered at the time of correction. Group 4 rats were subjected to 360o uterine torsion and melatonin was administered 6 h later at the time of correction. Group 5 was administered melatonin followed by uterine torsion of 360 degrees followed by correction of torsion 6 h later. Samples were obtained from the uterine horns on the day 1 postpartum. We used Bax, Bcl-2 and caspase 3 staining to measure apoptosis in the uterine tissues. The mRNA levels of Rho-associated, coiled-coil containing protein kinases 1 (ROCK1), homeobox D10 (Hox4 HoxD10), TLR4, NF kappa B1, caveolin 1 (Cav1) heat shock protein 90 alpha (cytosolic), class B member 1 (Hsp90ab1) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were determined using quantitative real-time polymerase chain reaction analysis (qRT-PCR). Bax, Bcl-2 and caspase 3 were detected using immunohistochemistry. No difference was observed among groups with respect to abortion, neonatal mortality or congenital abnormalities. Compared to the control group, the mRNA levels of Rock1, Hox4, TLR4, NF kappa B1, Cav1 and Hsp90 genes were decreased significantly in the study groups; the decrease was greater in groups 3 and 4, which were treated with melatonin. The greatest amount of Bax staining was found in group 1 and the least amount of Bcl-2 staining was found in groups 4 and 5; the greatest amount of caspase 3 staining was found in group 2. Our findings indicate that melatonin reduced uterine torsion related tissue damage and that its application during torsion was more effective than application following removal of torsion.en_US
dc.language.isoengen_US
dc.publisherTaylor and Francis Ltden_US
dc.relation.isversionof10.1080/10520295.2019.1605456en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectIschemiaen_US
dc.subjectMelatoninen_US
dc.subjectRaten_US
dc.subjectReperfusionen_US
dc.subjectTorsionen_US
dc.subjectUterusen_US
dc.titleEffect of melatonin on torsion and reperfusion induced pathogenesis of rat uterusen_US
dc.typearticleen_US
dc.relation.journalBiotechnic & Histochemistryen_US
dc.contributor.departmentVeteriner Fakültesien_US
dc.contributor.authorID0000-0001-5653-0025en_US
dc.contributor.authorID0000-0003-1365-1729en_US
dc.contributor.authorID0000-0002-8135-6142en_US
dc.identifier.volume94en_US
dc.identifier.issue7en_US
dc.identifier.startpage533en_US
dc.identifier.endpage539en_US
dc.relation.tubitak115O381
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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