The in-vivo assessment of Turkish propolis and its nano form on testicular damage induced by cisplatin

dc.contributor.authorSeven, Pinar Tatli
dc.contributor.authorSeven, Ismail
dc.contributor.authorKarakus, Selcan
dc.contributor.authorMutlu, Seda Iflazoglu
dc.contributor.authorKaya, Seyma Ozer
dc.contributor.authorArkali, Gozde
dc.contributor.authorKilislioglu, Ayben
dc.date.accessioned2026-08-12T18:07:01Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractObjective: Chemotherapeutic drugs, such as cisplatin (CP), which are associated with oxidative stress and apoptosis, may adversely affect the reproductive system. This study tests whether administration of propolis and nano-propolis (NP) can alleviate oxidative stress and apoptosis in rats with testicular damage induced by CP. Methods: In this study, polymeric nanoparticles including propolis were synthesized with a green sonication method and characterized using Fourier transform-infrared spectroscopy, Brunauer-EmmettTeller, and wet scanning transmission electron microscopy techniques. In total, 56 rats were divided into the following seven groups: control, CP, propolis, NP-10, CP + propolis, CP + NP-10, and CP + NP-30. Propolis (100 mg/kg), NP-10 (10 mg/kg), and NP-30 (30 mg/kg) treatments were administered by gavage daily for 21 d, and CP (3 mg/kg) was administered intraperitoneally in a single dose. After the experiment, oxidative stress parameters, namely, malondialdehyde (MDA), glutathione (GSH), glutathione peroxidase (GPx), and catalase (CAT), and apoptotic pathways including B cell leukemia/lymphoma-2 protein (Bcl-2) and Bcl-2-associated X protein (Bax) were measured in testicular tissues. Furthermore, sperm quality and weights of the testis, epididymis, right cauda epididymis, seminal vesicles and prostate were evaluated. Results: Propolis and NP (especially NP-30) were able to preserve oxidative balance (decreased MDA levels and increased GSH, CAT, and GPx activities) and activate apoptotic pathways (decreased Bax and increased Bcl-2) in the testes of CP-treated rats. Sperm motility in the control, CP, and CP + NP-30 groups were 60%, 48.75%, and 78%, respectively (P < 0.001). Especially, NP-30 application completely corrected the deterioration in sperm features induced by CP. Conclusion: The results show that propolis and NP treatments mitigated the side effects of CP on spermatogenic activity, antioxidant situation, and apoptosis in rats. (C) 2021 Shanghai Yueyang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine. Published by ELSEVIER B.V. All rights reserved.
dc.description.sponsorshipScientific and Technological Research Council of Turkey [118O112]
dc.description.sponsorshipThis study was funded by the Scientific and Technological Research Council of Turkey (No. 118O112).
dc.identifier.doi10.1016/j.joim.2021.08.002
dc.identifier.endpage459
dc.identifier.issn2095-4964
dc.identifier.issue5
dc.identifier.orcid0000-0003-1392-5056
dc.identifier.orcid0000-0001-6115-4458
dc.identifier.orcid0000-0002-8368-4609
dc.identifier.orcid0000-0002-6835-2171
dc.identifier.orcid0000-0003-2119-1216
dc.identifier.orcid0000-0002-9970-9364
dc.identifier.orcid0000-0003-0717-7637
dc.identifier.pmid34417154
dc.identifier.scopus2-s2.0-85112811609
dc.identifier.scopusqualityQ1
dc.identifier.startpage451
dc.identifier.urihttps://doi.org/10.1016/j.joim.2021.08.002
dc.identifier.urihttps://hdl.handle.net/11508/62542
dc.identifier.volume19
dc.identifier.wosWOS:000703056700008
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Integrative Medicine-Jim
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectCisplatin
dc.subjectNano-propolis
dc.subjectReproductive system
dc.subjectTesticular damage
dc.titleThe in-vivo assessment of Turkish propolis and its nano form on testicular damage induced by cisplatin
dc.typeArticle

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