PUBLICATION

Exposure to echimidine impairs the heart development and function of zebrafish larvae

Authors
Lin, T., Zhou, L., Chen, Z., Wang, L., Yang, J., Wang, S., Chen, X., Zuo, Z., He, C., Guo, L.
ID
ZDB-PUB-231017-50
Date
2023
Source
Ecotoxicology and environmental safety   266: 115574115574 (Journal)
Registered Authors
He, Chengyong, Yang, Jian
Keywords
Calcium signaling, Cardiac development, Pyrrolizidine alkaloid, Safety assessment, Zebrafish
MeSH Terms
  • Animals
  • Atrial Fibrillation*
  • Embryo, Nonmammalian/metabolism
  • Humans
  • Larva
  • Pyrrolizidine Alkaloids*/metabolism
  • Zebrafish/metabolism
PubMed
37839186 Full text @ Ecotoxicol. Environ. Saf.
Abstract
Pyrrolizidine alkaloids (PAs) are a class of phytotoxins that are widely distributed and can be consumed by humans through their daily diets. Echimidine is one of the most abundant PAs, but its safety, particularly its effects on development, is not fully understood. In this study, we used a zebrafish model to assess the developmental toxicity of echimidine. Zebrafish embryos were exposed to echimidine at concentrations of 0.02, 0.2, and 2 mg/L for 96 h. Our study revealed that embryonic exposure to echimidine led to developmental toxicity, characterized by delayed hatching and reduced body length. Additionally, echimidine exposure had a notable impact on heart development in larvae, causing tachycardia and reducing stroke volume (SV)and cardiac output (CO). Upon exposing the transgenic zebrafish strain Tg(cmlc2:EGFP) to echimidine, we observed atrial dilation and thinning of the atrial wall in developing embryos. Moreover, our findings indicated abnormal expression of genes associated with cardiac development (including gata4, tbx5, nkx2.5 and myh6) and genes involved in calcium signaling pathways (such as cacna1aa, cacna1sa, ryr2a, ryr2b, atp2a2a, atp2a2b, slc8a1, slc8a3 and slc8a4a). In summary, our findings demonstrate that echimidine may impair cardiac development and function in zebrafish larvae by disrupting calcium transport, leading to developmental toxicity. These findings provide insights regarding the safety of products containing PAs in food and medicine.
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