Effects of nanoplastic on toxicity of azole fungicides (ketoconazole and fluconazole) in zebrafish embryos

The ubiquity of nanoplastics (NPs) raises concerns about their interactions and combined toxicity with other common contaminants. Although azoles are present throughout the natural environment, their interactions with NP are not well known. We investigated the effects of polystyrene (PS) NP on the toxicity of ketoconazole (KCZ) and fluconazole (FCZ) in zebrafish embryos using the developmental toxicity, oxidative-stress-related biochemical parameters, and expression of genes related to neurotoxicity (ache), cardiotoxicity (gata4, bmp4), in-flammation (il1b), oxidative stress (sod1, sod2, cyp1a), and apoptosis (bax, bcl2). Co-exposure to NP (1 mg/L) and KCZ/FCZ (1 mg/L) for 96 h reduced the hatching rate, survival rate, and heart rate and increased the malformation rate and catalase activity. The bax/bcl2 ratio, an apoptosis indicator, was higher after NP, KCZ, or FCZ treatment. However, the bax/bcl2 ratio after exposure to NP + KCZ or NP + FCZ was much higher than that after single ex-posure. Overall, the results indicated that NP aggravated the toxicity of azole by significantly increasing the reac-tive oxygen species, lipid peroxidation and altering the expression of oxidative-stress-and apoptosis-related genes. The interactive toxicity of PS NP with KCZ/FCZ reported in this study emphasises the need for caution in the release of azole fungicides in the environment. (c) 2021 Elsevier B.V. All rights reserved.

Automated summary

The study found that co-exposure to polystyrene nanoplastics (PS NP) and ketoconazole (KCZ) or fluconazole (FCZ) increased oxidative stress and apoptosis-related gene expression, exacerbating the toxicity of azoles. This highlights the need for caution in releasing azole fungicides in the environment.