Protective effects of enoxaparin treatment against uterus ischemia/reperfusion injury in rats

dc.authorid0000-0002-3049-529X
dc.authorid0000-0002-9186-4861
dc.authorid0000-0001-9110-8364
dc.authorid0000-0003-4351-1719
dc.authorid0000-0002-3223-7729
dc.contributor.authorLafcı, Duygu
dc.contributor.authorYaranoğlu, Mustafa Hilmi
dc.contributor.authorAltun, Eren
dc.contributor.authorGüler, Eray Metin
dc.contributor.authorUsta, Ceyda Sancaklı
dc.date.accessioned2026-03-13T10:57:27Z
dc.date.issued2025
dc.departmentBalıkesir Üniversitesi
dc.descriptionLafci, Duygu (Balikesir Author) Yaranoglu, Mustafa Hilmi (Balikesir Author)
dc.description.abstractPurpose: This study analyzed the protective effects of enoxaparin in rat uteruses by exposing the uterus to experimental ischemiareperfusion injury. Methods: Thirty female rats were homogenized by weight and cycle and divided into three groups: a control group, an ischemia-reperfusion (I/R) group, and an ischemia-reperfusion plus enoxaparin (I/R+E) group. An experimental uterine I/R model was established in the I/R and I/R+E groups. Unlike I/R group, all rats in the I/R+E group received subcutaneous enoxaparin at 0.5 mg/kg 2 hours before ischemia. In histopathological analysis, endometrial glandular and endo/myometrial stromal changes were scored according to the histopathological scoring system. Biochemically, catalase (CAT), superoxide dismutase (SOD) enzyme activities, and malondialdehyde (MDA) levels were measured in uterine tissues. Results: In histopathological analysis, all of the control group’s scores were lower than those of the other groups, except for necrosis (p < 0.05). There was no significant improvement in the glandular and stromal changes between I/R and I/R+E (p > 0.05). However, the I/R+E group showed significantly increased SOD and CAT activities and decreased MDA levels compared to the I/R group (p = 0.000). Conclusion: Although enoxaparin did not significantly improve histopathological injury, its potent antioxidant effects suggest a protective role against oxidative stress in uterine I/R injury.
dc.identifier.doihttps://doi.org/10.1590/acb407225
dc.identifier.endpage10
dc.identifier.issn1678-2674
dc.identifier.pmid41036936
dc.identifier.scopus2-s2.0-105017629231
dc.identifier.scopusqualityQ2
dc.identifier.startpage1
dc.identifier.urihttps://hdl.handle.net/20.500.12462/23486
dc.identifier.volume40
dc.identifier.wosWOS:001588070800001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakScopus
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
dc.relation.ispartofActa Cirúrgica Brasileira
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEnoxaparin
dc.subjectIschemia
dc.subjectReperfusion Injury
dc.subjectUterus
dc.subjectOxidative Stress
dc.titleProtective effects of enoxaparin treatment against uterus ischemia/reperfusion injury in rats
dc.typeArticle

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