Experimental analysis shows silica nanoparticles disrupt blood-brain barrier integrity and trigger neuroinflammation, indicating health risks.
Silica nanoparticles (SiO2-NPs) are increasingly detected in environmental and food systems, raising concerns about their potential health risks via dietary exposure. Neurotoxicity assessment of SiO2-NPs is a critical aspect, yet the mechanisms underlying their neurotoxic effects remain poorly understood. This study examined depression-like behaviors in mice following 21-day oral administration of three distinct-sized SiO2-NPs (1 μm, 300 nm, and 50 nm), with particular focus on microglia-neuron crosstalk. The results demonstrate that SiO2-NPs disrupt blood-brain barrier integrity, induce microglial release of inflammatory extracellular traps (ETs) accompanied by neuronal pyroptosis, and ultimately cause depression-like behaviors in mice, with effects negatively correlating with particle size. Mechanistically, SiO2-NPs uptake by microglia promoted ROS-driven M1/M2 polarization imbalance and ETs release, while neuronal pyroptosis was mediated via the ROS/NLRP3 axis. Coculture experiments confirmed that microglial ETs exacerbated neuronal pyroptosis, and neuronal pyroptosis induced M1 polarization of microglia and further ETs release, ultimately forming a domino effect of neuroinflammation. These findings clarify key mechanisms underlying SiO2-NPs-induced neurotoxicity, providing critical insights for exposure risk assessment in food applications.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: