Hexafluoropropylene oxide trimer acid, a perfluorooctanoic acid alternative, induces cardiovascular toxicity in zebrafish embryos

被引:0
作者
Sun S. [2 ]
Zhang L. [1 ,2 ]
Li X. [1 ,2 ]
Zang L. [3 ]
Huang L. [4 ]
Zeng J. [5 ]
Cao Z. [1 ]
Liao X. [1 ]
Zhong Z. [2 ]
Lu H. [1 ]
Chen J. [2 ]
机构
[1] Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases, Jiangxi Key Laboratory of Developmental Biology of Organs, Center for Clinical Research Center of the Affiliated Hospital of Jinggangshan University, Jiangxi, Ji'an
[2] Translational Research Institute of Brain and Brain-like Intelligence, Shanghai Key Laboratory of Anesthesiology and Brain Functional Modulation, Department of Pediatrics, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai
[3] State Environmental Protection Key Laboratory of Environmental Health Impact Assessment of Emerging Contaminants, School of Environmental Sciences and Engineering, Shanghai Jiao Tong University, Shanghai
[4] Department of Interventional and Vascular Surgery, Affiliated Hospital of Jinggangshan University, Jiangxi, Ji'an
[5] Department of Internal Medicine and Hematology, Affiliated Hospital of Jinggangshan University, Jiangxi, Ji'an
来源
Journal of Environmental Sciences (China) | 2024年 / 139卷
基金
中国国家自然科学基金;
关键词
Heart development; Hemopoiesis; Hexafluoropropylene oxide trimer acid; Vascular development; Zebrafish embryos;
D O I
10.1016/j.jes.2023.05.009
中图分类号
学科分类号
摘要
As an increasingly used alternative to perfluorooctanoic acid (PFOA), hexafluoropropylene oxide trimer acid (HFPO-TA) has been widely detected in global water environments. However, little is known regarding its toxic effects on cardiovascular development. Here, zebrafish embryos were treated with egg water containing 0, 60, 120, or 240 mg/L HFPO-TA. Results showed that HFPO-TA treatment led to a significant reduction in both larval survival percentage and heart rate. Furthermore, HFPO-TA exposure caused severe pericardial edema and elongation of the sinus venous to bulbus arteriosus distance (SV-BA) in Tg (myl7: GFP) transgenic larvae, disrupting the expression of genes involved in heart development and thus causing abnormal heart looping. Obvious sprouting angiogenesis was observed in the 120 and 240 mg/L exposed Tg (fli: GFP) transgenic larvae. HFPO-TA treatment also impacted the mRNA levels of genes involved in the vascular endothelial growth factor (VEGF) pathway and embryonic vascular development. HFPO-TA exposure significantly decreased erythrocyte number in Tg (gata1: DsRed) transgenic embryos and influenced gene expression associated with the heme metabolism pathway. HFPO-TA also induced oxidative stress and altered the transcriptional levels of genes related to cell cycle and apoptosis, inhibiting cell proliferation while promoting apoptosis. Therefore, HFPO-TA exposure may induce abnormal development of the cardiovascular and hematopoietic systems in zebrafish embryos, suggesting it may not be a suitable or safe alternative for PFOA. © 2023
引用
收藏
页码:460 / 472
页数:12
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