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Genotoxicity and oxidative stress induction by calcium hydroxide, calcium titanate or/and yttrium oxide nanoparticles in mice
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Genotoxicity and oxidative stress induction by calcium hydroxide, calcium titanate or/and yttrium oxide nanoparticles in mice
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Journal Article
Genotoxicity and oxidative stress induction by calcium hydroxide, calcium titanate or/and yttrium oxide nanoparticles in mice
2023
Overview
Intensive uses of Calcium hydroxide (Ca(OH)
2
NPs), calcium titanate (CaTiO
3
NPs) and yttrium oxide (Y
2
O
3
NPs) nanoparticles increase their environmental release and human exposure separately or together through contaminated air, water and food. However, too limited data are available on their genotoxicity. Therefore, this study explored the effect of Ca(OH)
2
NPs, CaTiO
3
NPs or/and Y
2
O
3
NPs administration on the genotoxicityand oxidative stress induction in mice hepatic tissue. Mice were orally administered Ca(OH)
2
NPs, CaTiO
3
NPs and Y
2
O
3
NPs separately or simultaneously together at a dose level of 50 mg/kg b.w. for two successive weeks (3 days per week). Marked induction of DNA damage noticed after oral administration of Ca(OH)
2
NPs or CaTiO
3
NPs alone together with high Ca(OH)
2
NPs induced reactive oxygen species (ROS) generation and a slight CaTiO
3
NPs induced ROS production were highly decreased after simultaneous coadministration of administration of Y
2
O
3
NPs with Ca(OH)
2
NPs and CaTiO
3
NPs up to the negative control level. Oral administration of Y
2
O
3
NPs alone also did not cause observable changes in the genomic DNA integrity and the ROS generation level compared to the negative control levels. Similarly, significant elevations in P53 gene expression and high reductions in Kras and HSP-70 genes expression were observed only after administration of Ca(OH)
2
NPs alone, while, remarkable increases in the Kras and HSP-70 genes expression and non-significant changes in p53 gene expression were noticed after administration of CaTiO
3
NPs and Y
2
O
3
NPs separately or simultaneously together with Ca(OH)
2
NPs. Conclusion: Ca(OH)
2
NPs exhibited the highest genotoxic effect through oxidative stress induction and disruption of apoptotic (p53 and Kras) and protective (HSP-70) genes expression. Slight DNA damage was noticed after CaTiO
3
NPs administration. However, administration of Y
2
O
3
NPs alone was non-genotoxic and coadministration of Y
2
O
3
NPs with Ca(OH)
2
NPs and CaTiO
3
NPs restored genomic DNA integrity and normal expression of apoptotic p53 and protective HSP-70 genes disrupted by Ca(OH)
2
NPs and CaTiO
3
NPs. Thus co-administration of Y
2
O
3
NPs with Ca(OH)
2
NPs and CaTiO
3
NPs is recommended to counter Ca(OH)
2
NPs and CaTiO
3
NPs induced genotoxicity and oxidative stress.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
