Effect of thiamine pyrophosphate on cyclophosphamide-induced oxidative ovarian damage and reproductive dysfunction in female rats

ArticleAçık Erişim

Özet

Background. Cyclophosphamide is a drug used in various types of cancer. It can cause oxidative and inflammatory ovarian damage and infertility. Thiamine pyrophosphate (TPP) to be investigated for its effect on cyclophosphamide-induced ovarian damage and reproductive dysfunction in the present study is the active metabolite of thiamine. It has been shown that TPP protects organs and tissues from oxidative stress and proinflammatory cytokine damage. Objectives. To investigate the effect of TPP against the ovarian damage and reproductive dysfunction caused by cyclophosphamide in rats. Materials and methods. Albino Wistar type female rats were divided into healthy control (HG), cyclophosphamide (CYC) and TPP + cyclophosphamide (TPPC) groups (for each group, n = 12). Thiamine pyrophosphate at a dose of 25 mg/kg was injected intraperitoneally (ip.) in the TPPC group, and 0.9% NaCI solution was injected ip. in the CYC and HG groups. One hour after the injection, 75 mg/kg of cyclophosphamide was administered ip. in the TPPC and CYC groups. This procedure was repeated once a day for 30 days. At the end of this period, 6 rats from each group were euthanized with a high dose of anesthetic (50 mg/kg of sodium thiopental). Biochemical and histopathological examinations were performed on the extracted ovarian tissue. The remaining animals were kept in the laboratory with mature male rats for 2 months for reproduction. Results. Thiamine pyrophosphate significantly decreased the cyclophosphamide-induced increase in the levels of the oxidant parameter malondialdehyde (MDA), proinflammatory nuclear factor kappa B (NF-κB), tumor necrosis factor alpha (TNF-α), and interleukin 1 beta (IL-1β). In addition, TPP decreased the severe histopathological damage associated with cyclophosphamide in the ovarian tissue and prevented infertility. Conclusions. Our experimental results have suggested that TPP could be beneficial in the treatment of cyclophosphamide-induced ovarian injury and infertility. © 2022 by Wroclaw Medical University

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12601Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/142535Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorOzer, Mehmet
dc.contributor.authorInce, Sefa
dc.contributor.authorGundogdu, Betul
dc.contributor.authorAktas, Mehmet
dc.contributor.authorUzel, Kemine
dc.contributor.authorGursul, Cebrail
dc.contributor.authorSuleyman, Halis
dc.contributor.authorSuleyman, Zeynep
dc.date.accessioned2026-10-18T20:27:28.962967625Z
dc.date.available2026-10-18T20:27:28.962967625Z
dc.date.issued2022
dc.description.abstractBackground. Cyclophosphamide is a drug used in various types of cancer. It can cause oxidative and inflammatory ovarian damage and infertility. Thiamine pyrophosphate (TPP) to be investigated for its effect on cyclophosphamide-induced ovarian damage and reproductive dysfunction in the present study is the active metabolite of thiamine. It has been shown that TPP protects organs and tissues from oxidative stress and proinflammatory cytokine damage. Objectives. To investigate the effect of TPP against the ovarian damage and reproductive dysfunction caused by cyclophosphamide in rats. Materials and methods. Albino Wistar type female rats were divided into healthy control (HG), cyclophosphamide (CYC) and TPP + cyclophosphamide (TPPC) groups (for each group, n = 12). Thiamine pyrophosphate at a dose of 25 mg/kg was injected intraperitoneally (ip.) in the TPPC group, and 0.9% NaCI solution was injected ip. in the CYC and HG groups. One hour after the injection, 75 mg/kg of cyclophosphamide was administered ip. in the TPPC and CYC groups. This procedure was repeated once a day for 30 days. At the end of this period, 6 rats from each group were euthanized with a high dose of anesthetic (50 mg/kg of sodium thiopental). Biochemical and histopathological examinations were performed on the extracted ovarian tissue. The remaining animals were kept in the laboratory with mature male rats for 2 months for reproduction. Results. Thiamine pyrophosphate significantly decreased the cyclophosphamide-induced increase in the levels of the oxidant parameter malondialdehyde (MDA), proinflammatory nuclear factor kappa B (NF-κB), tumor necrosis factor alpha (TNF-α), and interleukin 1 beta (IL-1β). In addition, TPP decreased the severe histopathological damage associated with cyclophosphamide in the ovarian tissue and prevented infertility. Conclusions. Our experimental results have suggested that TPP could be beneficial in the treatment of cyclophosphamide-induced ovarian injury and infertility. © 2022 by Wroclaw Medical University
dc.identifier.doi10.17219/acem/142535
dc.identifier.eissn2451-2680
dc.identifier.endpage137
dc.identifier.issn1899-5276
dc.identifier.issue2
dc.identifier.pmid35156781
dc.identifier.scopus2-s2.0-85125554476
dc.identifier.startpage129
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12601
dc.identifier.volume31
dc.identifier.wosWOS:000755193400001
dc.language.isoen
dc.publisherWroclaw University of Medicine
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCyclophosphamide
dc.subjectInfertility
dc.subjectOvarian
dc.subjectRat
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectFemale
dc.subjectGlutathione
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectThiamine Pyrophosphate
dc.subjectcocarboxylase
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectsodium chloride
dc.subjectthiopental
dc.subjecttumor necrosis factor
dc.subjectantioxidant
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectcontrolled study
dc.subjectdrug effect
dc.subjectdrug megadose
dc.titleEffect of thiamine pyrophosphate on cyclophosphamide-induced oxidative ovarian damage and reproductive dysfunction in female rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus21
rdl.citation.wos23
rdl.departmentDepartment of Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Obstetrics and Gynecology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Physiology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Turkey. | Department of Nursing, Faculty of Health Sciences, Erzincan Binali Yıldırım University, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)