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Furan impairs cell function by inducing oxidative stress, DNA damage and apoptosis in mouse Sertoli cells in vitro
Yasemin Aydin1, Yasemin Ulku Dikbasan2, Banu Orta-Yilmaz1
1Department of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey.
Abstract:
Research on heat-induced food contaminants, such as furan, has shown its harmful effects on various systems. However, the impact of furan on Sertoli cells, a crucial male reproductive system cell, has not been studied. The investigation involved the treatment of furan to TM4 Sertoli cells at various concentrations (750, 1500, and 3000 µM) over a period of 24 h. This in vitro study determined that furan causes a decrease in Sertoli cell viability and an increase in lactate dehydrogenase activity, leading to cytotoxicity. Additionally, we observed an increase in MDA, one of the oxidative stress markers, in Sertoli cells, indicating that furan exposure leads to lipid peroxidation. It was determined that enzyme activities in the antioxidant defense system in Sertoli cells decreased after furan exposure. The findings indicate that furan induces oxidative damage in Sertoli cells by impairing the activity of antioxidant enzymes and promoting the production of ROS. This study discovered that furan triggers apoptosis in Sertoli cells by damaging DNA and altering the expression levels of apoptotic genes. Moreover, results suggest that furan causes cellular toxicity and apoptosis, leading to damage to Sertoli cells and thus causing male infertility.
Insights
Furan exposure damages male reproductive Sertoli cells, decreasing viability and inducing oxidative stress and apoptosis. This research highlights furan
Area of Science:
- Toxicology
- Reproductive Biology
- Cell Biology
Background:
- Furan is a heat-induced food contaminant with known systemic toxicity.
- Sertoli cells are vital for male reproductive function.
- The specific impact of furan on Sertoli cells remains uninvestigated.
Purpose of the Study:
- To investigate the toxic effects of furan on TM4 Sertoli cells *in vitro*.
- To determine furan's impact on Sertoli cell viability, oxidative stress, and apoptosis.
Main Methods:
- TM4 Sertoli cells were exposed to varying concentrations of furan (750, 1500, 3000 µM) for 24 hours.
- Cell viability, lactate dehydrogenase activity, malondialdehyde (MDA) levels, antioxidant enzyme activity, and apoptotic gene expression were assessed.
Main Results:
- Furan exposure significantly decreased Sertoli cell viability and increased cytotoxicity, evidenced by elevated lactate dehydrogenase.
- Furan induced oxidative stress, indicated by increased MDA levels and reduced antioxidant enzyme activities.
- Furan triggered apoptosis in Sertoli cells through DNA damage and altered apoptotic gene expression.
Conclusions:
- Furan causes significant cytotoxicity and oxidative damage to Sertoli cells.
- Furan induces apoptosis in Sertoli cells, potentially leading to male infertility.
- This study underscores the reproductive risks associated with furan exposure.
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