Abstract
Simple Summary
Waterborne exposure of Nile tilapia (Oreochromis niloticus) juveniles to sub-lethal concentrations of silicon dioxide nanoparticles (SiO(2)NPs) induced hepato-renal damage through elevation of aspartate transaminase (AST), alanine transaminase (ALT), and alkaline phosphatase (ALP) activities as well as creatinine and blood urea levels. SiO(2)NPs induced irreversible dose-dependent histopathological changes in the hepatopancreas, gills, and posterior kidneys, alongside modulation of the pro-inflammatory cytokines, apoptosis-related genes, and oxidative stress genes in gills and liver of exposed fish.
The current investigation assessed the impacts of sub-lethal concentrations of silicon dioxide nanoparticles (SiO(2)NPs) on hepato-renal functions, histopathological characteristics, and gene transcription in gills and liver of Nile tilapia juveniles. Fish were exposed to 20, 40, and 100 mg/L of SiO(2)NPs for 3 weeks. Pairwise comparisons with the control group showed a significant dose-dependent elevation in serum ALP, ALT, and AST enzyme activities as well as blood urea and creatinine levels in SiO2NP-intoxicated groups. Exposure to 100 mg/L SiO(2)NPs significantly upregulated expression of HSP70, TNF-alpha, IL-1 beta, and IL-8 genes in the gills as compared to the control group. Moreover, exposure to 100 mg/L SiO(2)NPs significantly upregulated the expression SOD, HSP70, IL-1 beta, IL-8, and TNF-alpha genes in the hepatic tissues as compared to the control group. Exposure of fish to 20 mg SiO(2)NPs/L significantly increased the mRNA expression levels of IL-12 in both the gills and liver tissues. Notably, all tested SiO2NP concentrations significantly upregulated the transcription of CASP3 gene in gills and liver of Nile tilapia as compared to the control group. Interestingly, varying histopathological alterations in renal, hepatopancreatic, and branchial tissues were observed to be correlated to the tested SiO2NP concentrations. In conclusion, our results provide additional information on the toxic impacts of SiO(2)NPs in Nile tilapia at the hematological, tissue, and molecular levels.