As a newly-invented and highly-efficiency
strobilurin fungicide,
pyraoxystrobin (SYP-3343) has been recognized as a highly poisonous toxin for a variety of aquatic organisms. Nevertheless, the developmental toxicity and potential mechanism of
SYP-3343 have not been well-documented. The results showed that
SYP-3343 was relatively stable and maintained within the range of 20 % in 24 h, and the LC50 value to embryos at 72 hpf was 17.13 μg/L. The zebrafish embryotoxicity induced by 1, 2, 4, and 8 μg/L
SYP-3343 is demonstrated by repressive embryo incubation, enhancive mortality rate, abnormal heart rate, malformed morphological characteristic, and impaired spontaneous coiling, indicating
SYP-3343 mostly exerted its toxicity in a dose- and time-dependent manner. Besides
SYP-3343 was critically involved in regulating cell cycle, mitochondrial membrane potential, and
reactive oxygen species production as well as zebrafish primary cells apoptosis, which can be mitigated using
antioxidant N-acetyl-L-cysteine. A significant change occurred in total
protein content, the biochemical indices, and
antioxidant capacities owing to
SYP-3343 exposure. Additionally,
SYP-3343 altered the
mRNA levels of heart development-, mitochondrial function-, and apoptosis-related genes in zebrafish embryos. These results indicated that
SYP-3343 induced apoptosis accompanying
reactive oxygen species-initiated
mitochondrial dysfunction in zebrafish embryos.