Gentisic acid attenuates 5-fluorouracil-induced ovotoxicity in rats via modulating Nrf2 signalling: An experimental approach
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Erişim
info:eu-repo/semantics/closedAccessTarih
2024Yazar
Menteşe, AhmetDemir, Selim
Yuluğ, Esin
Küçük, Hatice
Alemdar, Nihal Türkmen
Demir, Elif Ayazoğlu
Aliyazıcıoğlu, Yüksel
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Mentese, 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.2024.108661Özet
5-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.