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Gentisic acid attenuates 5-fluorouracil-induced ovotoxicity in rats via modulating Nrf2 signalling: An experimental approach.
Mentese, Ahmet; Demir, Selim; Yulug, Esin; Kucuk, Hatice; Alemdar, Nihal Turkmen; Demir, Elif Ayazoglu; Aliyazicioglu, Yuksel.
Afiliação
  • Mentese A; Department of Medical Services and Techniques, Vocational School of Health Services, Karadeniz Technical University, Trabzon 61080, Turkiye.
  • Demir S; Department of Nutrition and Dietetics, Faculty of Health Sciences, Karadeniz Technical University, Trabzon 61080, Turkiye. Electronic address: selim-demir@hotmail.com.
  • Yulug E; Department of Histology and Embryology, Faculty of Medicine, Karadeniz Technical University, Trabzon 61080, Turkey.
  • Kucuk H; Department of Pathology, Kanuni Training and Research Hospital, University of Health Sciences, Trabzon 61250, Turkiye.
  • Alemdar NT; Department of Medical Biochemistry, Graduate School of Health Sciences, Karadeniz Technical University, Trabzon 61080, Turkiye; Department of Medical Services and Techniques, Vocational School of Health Services, Recep Tayyip Erdogan University, Rize 53100, Turkiye.
  • Demir EA; Department of Chemistry and Chemical Processing Technologies, Macka Vocational School, Karadeniz Technical University, Trabzon 61750, Turkiye.
  • Aliyazicioglu Y; Department of Medical Biochemistry, Faculty of Medicine, Karadeniz Technical University, Trabzon 61080, Turkey.
Reprod Toxicol ; 128: 108661, 2024 09.
Article em En | MEDLINE | ID: mdl-38986848
ABSTRACT
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 dose-dependently 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ovário / Transdução de Sinais / Apoptose / Fluoruracila / Gentisatos Limite: Animals Idioma: En Revista: Reprod Toxicol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ovário / Transdução de Sinais / Apoptose / Fluoruracila / Gentisatos Limite: Animals Idioma: En Revista: Reprod Toxicol Ano de publicação: 2024 Tipo de documento: Article