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dc.contributor.authorMenteşe, Ahmet
dc.contributor.authorDemir, Selim
dc.contributor.authorYuluğ, Esin
dc.contributor.authorKüçük, Hatice
dc.contributor.authorAlemdar, Nihal Türkmen
dc.contributor.authorDemir, Elif Ayazoğlu
dc.contributor.authorAliyazıcıoğlu, Yüksel
dc.date.accessioned2024-08-12T08:02:02Z
dc.date.available2024-08-12T08:02:02Z
dc.date.issued2024en_US
dc.identifier.citationMentese, A., Demir, S., Yulug, E., Kucuk, H., Alemdar, N. T., Demir, E. A., & Aliyazicioglu, Y. (2024). Gentisic acid attenuates 5-flourouracil-induced ovotoxicity in rats via modulating Nrf2 signalling: An experimental approach. Reproductive Toxicology, 108661. https://doi.org/10.1016/j.reprotox.2024.108661en_US
dc.identifier.issn0890-6238
dc.identifier.issn1873-1708
dc.identifier.urihttps://doi.org/10.1016/j.reprotox.2024.108661
dc.identifier.urihttps://hdl.handle.net/11436/9216
dc.description.abstract5-Fluorouracil (5-FU) is the third most used chemotherapeutic in the world with its anticancer effect resulting from its potential to block DNA replication. Like other cytotoxic agents, 5-FU has side effects on healthy tissues, and the reproductive system is among the tissues most affected by these undesirable effects. Gentisic acid (GEA) is a secondary metabolite that is abundant in fruits, vegetables and spices and has antioxidant activity. This study was conducted to investigate the toxicity of 5-FU in rat ovarian tissue and to determine the therapeutic activity of GEA on ovotoxicity caused by 5-FU. The results showed that 5-FU caused histopathological findings by suppressing Nrf2 pathway and accordingly increasing oxidative stress, inflammation, endoplasmic reticulum stress and apoptosis. However, GEA treatments after 5-FU application ameliorated 5-FU-induced ovotoxicity dosedependently through activation of Nrf2 pathway. All these findings provided strong evidence supporting the hypothesis that GEA treatment may have therapeutic effects against 5-FU-induced ovarian damage. However, the beneficial effect of GEA use in eliminating ovarian damage in women after 5-FU chemotherapy should continue to be investigated with more detailed molecular studies.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject5-Fluorouracilen_US
dc.subjectEndoplasmic reticulum stressen_US
dc.subjectGentisic aciden_US
dc.subjectInflammationen_US
dc.subjectNrf2en_US
dc.subjectOvotoxicityen_US
dc.subjectOxidative stressen_US
dc.titleGentisic acid attenuates 5-fluorouracil-induced ovotoxicity in rats via modulating Nrf2 signalling: An experimental approachen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.contributor.institutionauthorAlemdar, Nihal Türkmen
dc.identifier.doi10.1016/j.reprotox.2024.108661en_US
dc.identifier.volume128en_US
dc.identifier.startpage108661en_US
dc.relation.journalReproductive Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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