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dc.contributor.authorIsmık, Denizen_US
dc.contributor.authorSeven, Pnar Tatlıen_US
dc.contributor.authorYedi, İsmailen_US
dc.contributor.authorKarakuş, Selcanen_US
dc.contributor.authorMutlu, Seda İflazoğluen_US
dc.contributor.authorKaya, Şeyma Özeren_US
dc.contributor.authorArkalı, Gözdeen_US
dc.contributor.authorTan, Ezgien_US
dc.contributor.authorŞahin, Yeşim Mügeen_US
dc.contributor.authorKilislioğlu, Aybenen_US
dc.date.accessioned2021-09-22T08:35:16Z
dc.date.available2021-09-22T08:35:16Z
dc.date.issued2021en_US
dc.identifier.citationSeven, P. T., Seven, I., Karakus, S., Mutlu, S. I., Kaya, S. O., Arkali, G., ... & Kilislioglu, A. (2021). The in-vivo assessment of Turkish propolis and its nano form on testicular damage induced by cisplatin. Journal of Integrative Medicine.en_US
dc.identifier.urihttps://doi.org/10.1016/j.joim.2021.08.002
dc.identifier.urihttps://hdl.handle.net/20.500.12294/2846
dc.description.abstractChemotherapeutic 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. In this study, polymeric nanoparticles including propolis were synthesized with a green sonication method and characterized using Fourier transform-infrared spectroscopy, Brunauer-Emmett-Teller, 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. 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. The results show that propolis and NP treatments mitigated the side effects of CP on spermatogenic activity, antioxidant situation, and apoptosis in rats.en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofJournal of Integrative Medicineen_US
dc.identifier.doi10.1016/j.joim.2021.08.002en_US
dc.identifier.doi10.1016/j.joim.2021.08.002
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCisplatinen_US
dc.subjectNano-propolisen_US
dc.subjectReproductive Systemen_US
dc.subjectTesticular Damageen_US
dc.titleThe in-vivo Assessment of Turkish Propolis and its Nano form on Testicular Damage Induced by Cisplatinen_US
dc.typearticleen_US
dc.departmentRektörlüken_US
dc.identifier.startpage1en_US
dc.identifier.endpage9en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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