N-acetylcysteine ameliorates 5-fluorouracil-induced ovarian injury in rats
Göster/ Aç
Erişim
info:eu-repo/semantics/openAccessTarih
2023Yazar
Demir, Elif AyazoğluMenteşe, Ahmet
Küçük, Hatice
Alemdar, Nihal Türkmen
Demir, Selim
Aliyazıcıoğlu, Yüksel
Üst veri
Tüm öğe kaydını gösterKünye
Demir, E.A., Menteşe, A., Küçük, H., Alemdar, N.T., Demir, S. & Aliyazıcıoğlu, Y. (2023). N-Acetylcysteine Ameliorates 5-Fluorouracil-Induced Ovarian Injury in Rats. Clinical and Experimental Health Sciences, 13(4), 776-781. https://doi.org/10.33808/clinexphealthsci.1199615Özet
Objective: Although 5-fluorouracil (5-FU) is one of the most commonly used chemotherapeutics worldwide, it has been shown that 5-FU administration can cause reproductive toxicity in recent years. N-acetylcysteine (NAC) is the precursor of glutathione, the most important endogenous antioxidant molecule and is known for its effective antioxidant and anti-inflammatory properties. Although NAC is one of the most studied antioxidant molecules, its curative effect against ovarian damage caused by 5-FU has not been demonstrated to date. It was therefore aimed to investigate whether NAC is therapeutic against 5-FU-induced ovotoxicity in this study for the first time.Methods: Rats were first exposed to a single dose of 5-FU (100 mg/kg) and then treated with NAC (10 and 20 mg/kg) for three days. The oxidative stress, inflammation and apoptosis markers in ovarian tissues were also determined using spectrophotometric methods. Ovarian tissues were also evaluated histologically.Results: It was revealed that the levels of oxidative stress, inflammation and apoptosis biomarkers in ovarian tissue increased by 5-FU administration (p<.005). Treatments with NAC significantly restored these damages dose-dependently (p<.005). Moreover, these biochemical findings were confirmed by histological examination.Conclusion: NAC can be considered as a potential therapeutic molecule against 5-FU-induced reproductive toxicity, as it can abolish the ovarian toxicity caused by 5-FU by reducing oxidative stress, inflammation and apoptosis.