Aydin Yasemin, Dikbasan Yasemin Ulku, Orta-Yilmaz Banu
Department of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey.
Institute of Graduate Studies in Science and Engineering, Department of Biology, Istanbul University, Istanbul, Turkey.
Drug Chem Toxicol. 2025 Sep;48(5):1067-1079. doi: 10.1080/01480545.2024.2437056. Epub 2024 Dec 16.
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 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.
对热诱导的食品污染物(如呋喃)的研究表明,其对各种系统都有有害影响。然而,呋喃对睾丸支持细胞(一种关键的雄性生殖系统细胞)的影响尚未得到研究。该研究涉及在24小时内用不同浓度(750、1500和3000µM)的呋喃处理TM4睾丸支持细胞。这项研究确定,呋喃会导致睾丸支持细胞活力下降和乳酸脱氢酶活性增加,从而导致细胞毒性。此外,我们观察到睾丸支持细胞中氧化应激标志物之一丙二醛(MDA)增加,这表明接触呋喃会导致脂质过氧化。研究确定,呋喃暴露后,睾丸支持细胞抗氧化防御系统中的酶活性降低。研究结果表明,呋喃通过损害抗氧化酶的活性和促进活性氧(ROS)的产生,在睾丸支持细胞中诱导氧化损伤。这项研究发现,呋喃通过破坏DNA和改变凋亡基因的表达水平,触发睾丸支持细胞的凋亡。此外,结果表明,呋喃会导致细胞毒性和凋亡,从而损害睾丸支持细胞,进而导致男性不育。