Can pycnogenol prevent cisplatin-induced damage in uterus and ovaries?

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Özet

Introduction: Cisplatin is an antineoplastic agent, which is thought to act on tissues with increased levels of reactive oxygen species and decreased levels of antioxidants. Pycnogenol is a potent antioxidant that is used in medical conditions caused by oxidative stress. The aim of our study is to demonstrate the effects of pycnogenol on cisplatin-induced uterine and ovarian damage in rats. Material and methods: Wistar albino female rats were randomly divided into 3 groups before the experiment as follows: a 2.5 mg/kg cisplatin group (CG; n = 10), a 40 mg/kg pycnogenol + 2.5 mg/kg cisplatin group (PCG; n = 10), and a healthy control group (HG; n = 10). Then, the ovaries and uteri of the rats were examined to determine malondialdehyde (MDA), total glutathione (tGSH) and superoxide dismutase (SOD) biochemical levels and the histopathological findings. Results: Our study demonstrated that, in uterine and ovarian tissues of rats administered with cisplatin, there was a decrease in the levels of tGSH and SOD, while MDA was increased; however, it was observed that these ratios were reversed in the PCG group (p < 0.05). The number of follicles in the ovarian tissues was examined in all 3 groups. When the CG group was compared with the other two groups, the number of primordial, developing and atretic follicles was low, but there was no difference in the corpus luteum count. Conclusions: Pycnogenol pretreatment alleviates cisplatin-induced uterine and ovarian injury in rats because of its antioxidative effect. Copyright © 2019 Termedia & Banach.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12814Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.5114/aoms.2019.90414Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTurkler, Can
dc.contributor.authorKiremitli, Tunay
dc.contributor.authorOnat, Taylan
dc.contributor.authorYildirim, Engin
dc.contributor.authorYazici, Gulce N.
dc.contributor.authorMammadov, Renad
dc.contributor.authorSunar, Mukadder
dc.date.accessioned2026-10-18T20:27:40.892284007Z
dc.date.available2026-10-18T20:27:40.892284007Z
dc.date.issued2022
dc.description.abstractIntroduction: Cisplatin is an antineoplastic agent, which is thought to act on tissues with increased levels of reactive oxygen species and decreased levels of antioxidants. Pycnogenol is a potent antioxidant that is used in medical conditions caused by oxidative stress. The aim of our study is to demonstrate the effects of pycnogenol on cisplatin-induced uterine and ovarian damage in rats. Material and methods: Wistar albino female rats were randomly divided into 3 groups before the experiment as follows: a 2.5 mg/kg cisplatin group (CG; n = 10), a 40 mg/kg pycnogenol + 2.5 mg/kg cisplatin group (PCG; n = 10), and a healthy control group (HG; n = 10). Then, the ovaries and uteri of the rats were examined to determine malondialdehyde (MDA), total glutathione (tGSH) and superoxide dismutase (SOD) biochemical levels and the histopathological findings. Results: Our study demonstrated that, in uterine and ovarian tissues of rats administered with cisplatin, there was a decrease in the levels of tGSH and SOD, while MDA was increased; however, it was observed that these ratios were reversed in the PCG group (p < 0.05). The number of follicles in the ovarian tissues was examined in all 3 groups. When the CG group was compared with the other two groups, the number of primordial, developing and atretic follicles was low, but there was no difference in the corpus luteum count. Conclusions: Pycnogenol pretreatment alleviates cisplatin-induced uterine and ovarian injury in rats because of its antioxidative effect. Copyright © 2019 Termedia & Banach.
dc.identifier.doi10.5114/aoms.2019.90414
dc.identifier.eissn1896-9151
dc.identifier.endpage1371
dc.identifier.issn1734-1922
dc.identifier.issue5
dc.identifier.pmcidPMC9479720
dc.identifier.pmid36160362
dc.identifier.scopus2-s2.0-85095723987
dc.identifier.startpage1364
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12814
dc.identifier.volume18
dc.identifier.wosWOS:000869187900024
dc.language.isoen
dc.publisherTermedia Publishing House Ltd.
dc.relation.ispartofArchives of Medical Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcisplatin
dc.subjectovary
dc.subjectoxidative stress
dc.subjectpycnogenol
dc.subjectrat
dc.subjectuterus
dc.subjectglutathione
dc.subjectmalonaldehyde
dc.subjectsuperoxide dismutase
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectbleeding
dc.subjectcell degeneration
dc.subjectcomparative study
dc.subjectcontrolled study
dc.subjectcorpus luteum
dc.subjectfemale
dc.subjecthistopathology
dc.subjecthuman
dc.subjecthyperemia
dc.subjectnonhuman
dc.subjectovary disease
dc.subjectovary follicle
dc.subjectovary follicle cell
dc.subjectovary tissue
dc.subjectprimordial follicle
dc.titleCan pycnogenol prevent cisplatin-induced damage in uterus and ovaries?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus6
rdl.citation.wos4
rdl.departmentDepartment of Gynecology and Obstetrics, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Histology and Embryology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey. | Department of Anatomy, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)