Using Caenorhabditis elegans as an animal model, we investigated combinational effect between 2-hydroxyatrazine (HA) and polystyrene nanoparticle (PS-NP) on function and development of D-type motor neurons. Exposure to HA (10 and 100 μg/L) alone caused decreases in body bend, head thrash, and forward turn and increase in backward turn. Exposure to 100 μg/L HA also caused neurodegeneration of D-type motor neurons. Moreover, combinational exposure to HA (0.1 and 1 μg/L) induced enhancement in PS-NP (10 μg/L) toxicity in inhibiting body bend, head thrash, and forward turn, and in increasing backward turn. In addition, combinational exposure to HA (1 μg/L) could result in neurodegeneration of D-type motor neurons in PS-NP (10 μg/L) exposed nematodes. Combinational exposure to HA (1 μg/L) and PS-NP (10 μg/L) increased expressions of crt-1, itr-1, mec-4, asp-3, and asp-4, which govern the induction of neurodegeneration. Moreover, combinational exposure to HA (0.1 and 1 μg/L) strengthened PS-NP (10 μg/L)-induced decreases in glb-10, mpk-1, jnk-1, and daf-7 expressions, which encode neuronal signals regulating response to PS-NP. Therefore, our results demonstrated the effect of combinational exposure to HA and nanoplastics at environmentally relevant concentrations in causing toxic effect on nervous system in organisms.
Keywords: C. elegans; Combinational exposure; Hydroxyatrazine; Nanoplastic.
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