Show simple item record

dc.contributor.authorErsoy, Gulcin Sahin
dc.contributor.authorEken, Meryem Kurek
dc.contributor.authorCevik, Ozge
dc.contributor.authorCilingir, Ozlem T.
dc.contributor.authorTal, Reshef
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:44:02Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:44:02Z
dc.date.issued2017
dc.identifier.issn1472-6483
dc.identifier.issn1472-6491
dc.identifier.urihttps://dx.doi.org/10.1016/j.rbmo.2016.11.007
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6873
dc.descriptionWOS: 000393171200001en_US
dc.descriptionPubMed ID: 27913135en_US
dc.description.abstractThis study evaluated the effect of mycophenolate mofetil (MMF) on uterine tissue preservation following ischaemia/reperfusion (I/R) injury. Uterine I/R injury was induced in rats by clamping the lower abdominal aorta and ovarian arteries for 30 min. Group I/R + V (n = 7) received vehicle alone while Group I/R + M (n = 7) received 20 mg/kg/day MMF. Control groups underwent sham surgery and received vehicle (Group C) or 20 mg/kg/day MMF (Group M) (n = 7 for both). Four hours after detorsion, uterine tissue 8-hydroxy-2'-deoxyguanosine (8-OHdG), glutathione, malondialdehyde (MDA), myeloperoxidase (MPO), superoxide dismutase (SOD) and serum ischaemia modified albumin (IMA) concentrations were measured. Histopathological analyses were performed. The I/R + M group showed significant reduction in serum IMA and uterine tissue 8-OHdG, MDA and MPO and significant increase in SOD concentrations compared with the I/R + V group, indicating a protective effect against I/R oxidative damage (P = 0.009, P = 0.006, P = 0.002, P = 0.003 and P = 0.009, respectively). Histopathological evaluation revealed MMF treatment resulted in significantly less tissue and cellular damage and apoptosis compared with the I/R + V group. These results indicate MMF is effective in attenuating uterine tissue damage and preventing apoptosis following uterine I/R injury, probably via anti-inflammatory and anti-oxidative action. (C) 2016 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCI LTDen_US
dc.relation.isversionof10.1016/j.rbmo.2016.11.007en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectmycophenolate mofetilen_US
dc.subjectoxygen species-free radicalsen_US
dc.subjectraten_US
dc.subjectuterine ischaemia-reperfusionen_US
dc.subjectuterine transplantationen_US
dc.titleMycophenolate mofetil attenuates uterine ischaemia/reperfusion injury in a rat modelen_US
dc.typearticleen_US
dc.relation.journalREPRODUCTIVE BIOMEDICINE ONLINEen_US
dc.contributor.department[Ersoy, Gulcin Sahin] Kartal Dr Lutfi Kirdar Educ & Res Hosp, Dept Obstet & Gynecol, Istanbul, Turkey -- [Eken, Meryem Kurek] Zeynep Kamil Educ & Res Hosp, Dept Obstet & Gynecol, Istanbul, Turkey -- [Cevik, Ozge] Cumhuriyet Univ, Fac Pharm, Dept Biochem, Sivas, Turkey -- [Cilingir, Ozlem T.] Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkey -- [Tal, Reshef] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, Div Reprod Endocrinol & Infertil, New Haven, CT USAen_US
dc.contributor.authorIDCilingir Kaya, Ozlem Tugce -- 0000-0002-2591-9174; Cevik, Ozge -- 0000-0002-9325-3757; Tal, Reshef -- 0000-0002-2500-9904; Sahin Ersoy, Gulcin -- 0000-0003-2354-3668en_US
dc.identifier.volume34en_US
dc.identifier.issue2en_US
dc.identifier.endpage123en_US
dc.identifier.startpage115en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record