Silica nanoparticles: Chemical synthesis and acute neurotoxic study in Wistar rat

Abstract

Objectives: In this study, silica nanoparticles (SNPs) were synthesized through the sol-gel approach, characterized using X-ray diffraction and examined for their potential to induce acute neurotoxicity in rats. Materials and Methods: The average particle size was confirmed to be 110 ± 5 nm through scanning electron microscope (SEM) analysis. An intraperitoneal injection of 25, 50, and 100 mg/kg of SNPs was administered twice over 24 h to rats, followed by autopsies 24 h later. Brain regions (cerebellum, frontal cortex, hippocampus, and corpus striatum) were analyzed for changes in antioxidant enzyme activity (superoxide dismutase [SOD], catalase [CAT], glutathione-s-transferase [GST], glutathione peroxidase [GPx], glutathione reductase [GR] and thiobarbituric acid reactive substance [TBARS] levels) and neurotransmitter concentrations (acetylcholinestrase [AChE], dopamine, serotonin and nor-epinephrine). Results: The activity of SOD, CAT and GST increased significantly in the high dose group, specifically in the hippocampus and corpus striatum. No significant change in GR activity was observed in any dose group. Significant alterations were observed in neurotransmitter concentrations in hippocampus and corpus striatum in rats treated with high dose. Conclusion: Overall, the outcomes derived from our research suggest that SNPs lead to dose-dependent oxidative harm and neurotoxic effects in different regions of brain.