Polystyrene microplastics enhance microcystin-LR-induced cardiovascular toxicity and oxidative stress in zebrafish embryos
Abstract
The health risks associated with combined exposure to microplastics (MPs) and cyanobacteria toxins have gained increasing attention due to the large-scale prevalence of cyanobacterial blooms and accumulation of MPs in aquatic environments. Therefore, we explored the cardiovascular toxic effects of microcystin-LR (MC-LR, 1, 10, 100 μg/L) in the presence of 5 μm polystyrene microplastics (PS-MPs, 100 μg/L) and 80 nm polystyrene nanoplastics (PS-NPs, 100μg/L) in zebrafish models. Embryos were exposed to certain PS-MPs and PS-NPs conditions in water between 3 h post-fertilization (hpf) and 168 hpf. Compared to MC-LR alone, a significant decrease in heart rate was observed as well as notable pericardial edema in the MC-LR+PS-MPs/NPs groups. At the same time, sinus venosus and bulbus arteriosus (SV-BA) distances were significantly increased. Furthermore, the addition of PS-MPs/NPs caused thrombosis in the caudal vein and more severe vascular damage in zebrafish larvae compared to MC-LR alone. Our findings revealed that combined exposure to PS-NPs and MC-LR could significantly decreased the expression of genes associated with cardiovascular development (myh6, nkx2.5, tnnt2a, and vegfaa), ATPase (atp1a3b, atp1b2b, atp2a1l, atp2b1a, and atp2b4), and the calcium channel (cacna1ab and ryr2a) compared to exposure to MC-LR alone. In addition, co-exposure with PS-MPs/NPs exacerbated the MC-LR-induced reactive oxygen species (ROS) production, as well as the ROS-stimulated apoptosis and heightened inflammation. We also discovered that astaxanthin (ASTA) treatment partially attenuated these cardiovascular toxic effects. Our findings confirm that exposure to MC-LR and PS-MPs/NPs affects cardiovascular development through calcium signaling interference and ROS-induced cardiovascular cell apoptosis. This study highlights the potential environmental risks of the co-existence of MC-LR and PS-MPs/NPs for fetal health, particularly cardiovascular development.
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- Authors
- Xiao, Y., Hu, L., Duan, J., Che, H., Wang, W., Yuan, Y., Xu, J., Chen, D., & Zhao, S.
- Affiliations
- Anhui Medical University (CN)
- Corresponding author
- Zhao, Sujuan
- Venue
- Environmental Pollution
- Publisher
- Elsevier BV
- Published
- 2024-07
- Volume
- 352
- Pages
- 124022
- ISSN
- 0269-7491 (ISSN-L)
- OpenAlex
- W4395661061
- Semantic Scholar
- 4b9fa9a9326818a5e7bf90fd250b806016773888
- Cited by
- 49
- References
- 72
- Citations by year
- 2026: 19 · 2025: 26 · 2024: 4
- FWCI
- 4.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Environmental Pollution (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Environmental Science › Pollution › Microplastics and Plastic Pollution
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Environmental Toxicology and Ecotoxicology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Keywords
- polystyrene microplastics, polystyrene nanoplastics, microcystin-LR, cyanotoxins, cardiotoxicity, zebrafish embryos, oxidative stress, reactive oxygen species, apoptosis, calcium signaling, heart development, vascular injury, thrombosis, pericardial edema, astaxanthin, combined exposure, cyanobacterial blooms
- MeSH terms
- Microplastics, Animals, Embryo, Nonmammalian, Marine Toxins, Polystyrenes, Water Pollutants, Chemical, Zebrafish, Oxidative Stress, Microcystins
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