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dc.contributor.authorAyazoğlu Demir, Elif
dc.contributor.authorMenteşe, Ahmet
dc.contributor.authorLivaoğlu, Ayten
dc.contributor.authorTürkmen Alemdar, Nihal
dc.contributor.authorDemir, Selim
dc.date.accessioned2022-10-17T06:15:13Z
dc.date.available2022-10-17T06:15:13Z
dc.date.issued2021en_US
dc.identifier.citationAyazoglu Demir, E., Mentese, A., Livaoglu, A., Turkmen Alemdar, N., & Demir, S. (2021). Ameliorative effect of gallic acid on cisplatin-induced ovarian toxicity in rats. Drug and chemical toxicology, 1–7. Advance online publication. https://doi.org/10.1080/01480545.2021.2011312en_US
dc.identifier.issn0148-0545
dc.identifier.issn1525-6014
dc.identifier.urihttps://doi.org/10.1080/01480545.2021.2011312
dc.identifier.urihttps://hdl.handle.net/11436/6767
dc.description.abstractThe aim of the present study was to evaluate the protective effect of gallic acid (GA) against cisplatin (CDDP)-induced ovarian toxicity, for the first time. The ovarian damage was generated with CDDP (5 mg/kg) intraperitoneally (i.p.) administration in rats. GA (2.5 and 5 mg/kg) were administered i.p. for 3 consecutive days. The study was carried out in 5 main groups containing 6 rats in each group: control, GA (5 mg/kg), CDDP, CDDP + GA (2.5 mg/kg) and CDDP + GA (5 mg/kg). The levels of ovarian malondialdehyde (MDA), total oxidant status (TOS), total antioxidant status (TAS), oxidative stress index (OSI), catalase (CAT), 8-hydroxy-2'-deoxyguanosine (8-OHdG), caspase-3 and tumor necrosis factor-alpha (TNF-alpha) were determined. Hematoxylin and eosin staining method was employed for the histopathological examination. In the CDDP group, it is determined that statistically significant decreasing in the levels of TAS and CAT, and increasing in the levels of MDA, TOS, OSI, 8-OHdG, caspase-3 and TNF-alpha (p < 0.05) compared with control group. GA administrations statistically significantly restored this damage (p < 0.05). Although vascular congestion, edema, hemorrhage, follicular degeneration and leukocyte infiltration were significantly higher in the CDDP group than in the control group, GA administrations statistically significantly restored these damages (p < 0.05). In conclusion, this study showed that GA prevented CDDP-induced ovarian damage with its antioxidant, anti-apoptotic and anti-inflammatory activities. More comprehensive studies are needed to see the underlying mechanisms.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltd.en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCisplatinen_US
dc.subjectGallic aciden_US
dc.subjectInflammationen_US
dc.subjectOvo-toxicityen_US
dc.subjectOxidative stressen_US
dc.subjectRaten_US
dc.titleAmeliorative effect of gallic acid on cisplatin-induced ovarian toxicity in ratsen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.contributor.institutionauthorTürkmen Alemdar, Nihal
dc.identifier.doi10.1080/01480545.2021.2011312en_US
dc.identifier.startpage1en_US
dc.identifier.endpage7en_US
dc.relation.journalDrug and Chemical Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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