Titanium dioxide nanoparticles (TiO NPs) are widely used for their whiteness and opacity in several applications such as food colorants, drug additives, biomedical ceramic, and implanted biomaterials. Research on the neurobiological response to orally administered TiO NPs is still limited. In our study, we investigate the effects of anatase TiO NPs on the brain of Wistar rats after oral intake. After daily intragastric administration of anatase TiO NPs (5-10 nm) at 0, 50, 100, and 200 mg/kg body weight (BW) for 60 days, the coefficient of the brain, acethylcholinesterase (AChE) activities, the level of interleukin 6 (IL-6), and the expression of glial fibrillary acidic protein (GFAP) were assessed to quantify the brain damage. The results showed that high-dose anatase TiO NPs could induce a downregulated level of AChE activities and showed an increase in plasmatic IL-6 level as compared to the control group accompanied by a dose-dependent decrease inter-doses, associated to an increase in the cerebral IL-6 level as a response to a local inflammation in brain. Furthermore, we observed elevated levels of immunoreactivity to GFAP in rat cerebral cortex. We concluded that oral intake of anatase TiO NPs can induce neuroinflammation and could be neurotoxic and hazardous to health.

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This work is devoted to the synthesis and study of the different properties of ZnO nanoparticles (NPs) doped with the Ni element.