Bisphenol F (BPF) exposure impairs sperm quality and offspring development in male zebrafish

被引:0
作者
Wu, Wenying [1 ]
Su, Zhongjing [2 ]
Luo, Congying [1 ]
Li, Jiejie [1 ]
Yu, Xinle [3 ]
Xie, Han [1 ]
Wu, Ganglong [1 ]
Wang, Dinghui [1 ]
Wu, Kusheng [1 ]
机构
[1] Shantou Univ, Dept Prevent Med, Med Coll, Shantou 515041, Guangdong, Peoples R China
[2] Shantou Univ, Dept Histol & Embryol, Med Coll, Shantou 515041, Guangdong, Peoples R China
[3] Shantou Univ, Mental Hlth Ctr, Shantou 515065, Guangdong, Peoples R China
关键词
Bisphenol F; Male zebrafish; Sperm; Hormones; apoptosis; Meiosis; UNITED-STATES; IN-VITRO; ANALOGS; SPERMATOGENESIS; ALTERNATIVES; SPERMATOZOA; PROFILES;
D O I
10.1016/j.taap.2025.117245
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Bisphenol F (BPF), a substitute for bisphenol A (BPA), is widely used in consumer products, increasing the potential for environmental exposure. Our study investigated the reproductive effects of BPF on adult male zebrafish and explored its toxicological mechanisms, as well as its intergenerational effects. Methods: Adult male zebrafish were exposed to BPF concentrations of 0, 50, 500, 2500, and 5000 nM for 21 days. We evaluated sperm cell quantity and quality, hormonal markers testosterone (T) and vitellogenin (VTG), gene expression profiles related to hormone synthesis, metabolism, apoptosis, cell cycle, sexual behavior, and offspring health metrics including survival, development and locomotion. Results: BPF exposure did not significantly affect body weight or gonadal index. However, at 500 and 2500 nM, a significant reduction in sperm count was observed. BPF exposure led to decreased serum T and increased hepatic VTG levels, indicating hormonal disruption. At 50 nM, BPF initiated sperm apoptosis, and at higher doses, it disrupted sperm meiosis, affecting cell distribution. This exposure negatively impacted sperm quality, reduced offspring survival rates, and altered sperm motility in adult fish. Offspring from BPF-exposed groups showed developmental issues, including increased mortality, delayed developmental stages, abnormal tail coiling and heart rate, which correlated with paternal sperm count and quality changes, alterations in T and VTG levels, and cell cycle phase distributions. Conclusions: Our study demonstrated that BPF exposure significantly impacted sperm quality, characterized by reduced sperm count and altered motility patterns, leading to developmental anomalies in offspring. These novel findings highlight the need for further research into BPF's reproductive and developmental toxicity, emphasizing the potential risks to aquatic ecosystems and human health. The observed effects on sperm quality, hormonal balance, and offspring development provide new insights into the reproductive toxicity profile of BPF.
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页数:13
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