Morphological and Transcriptomic Analyses Reveal the Toxicological Mechanism and Risk of Nitrate Exposure in Embryos.

In recent years, nitrate (NO-N) pollution in water bodies has been increasing due to the excessive use of nitrogen-based fertilizers. Exposure to NO-N during the development of amphibian embryos may have lasting effects on the growth and development of individuals and even threaten their survival, but the toxicity mechanism of NO-N in amphibian embryos prior to thyroid morphogenesis remains unclear. In the present study, was selected as the model organism to investigate the toxic effects of 10 mg/L and 100 mg/L NO-N exposure (N10 and N100) on amphibian embryos using methimazole (MMI) and exogenous thyroxine (T4) as the reference groups. We found that T4, MMI, N10 and N100 inhibited embryo growth and development, with MMI and N100 showing the earliest and strongest effects. Transcriptome analysis revealed that MMI and NO-N (especially N100) significantly downregulated genes related to thyroid morphogenesis and cholesterol metabolism, while upregulating genes related to inflammation and apoptosis. Together, these results contribute to a deeper understanding of the complex mechanisms by which NO-N disrupts embryonic development, reveal the potential risks of NO-N pollution to other aquatic organisms, and provide insights into the conservation of a broader ecosystem.