Journal
JOURNAL OF HAZARDOUS MATERIALS
Volume 195, Issue -, Pages 365-370Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhazmat.2011.08.055
Keywords
Titanium dioxide nanoparticules; Kidney; Inflammatory response; Cytokines
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Funding
- Priority Academic Program Development of Jiangsu Higher Education Institutions
- National Natural Science Foundation of China [30901218, 30671782, 30972504]
- Major State Basic Research Development Program of China (973 Program) [2006CB705602]
- National Important Project on Scientific Research of China [2011CB933404]
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Numerous studies have demonstrated that damage of kidney of mice can be caused by exposure to titanium dioxide nanoparticles (TiO2 NPs). However, the molecular mechanism of TiO2 NPs-induced nephric injury remains unclear. In this study, the mechanism of nephric injury in mice induced by an intragastric administration of TiO2 NPs was investigated. The results showed that TiO2 NPs were accumulated in the kidney, resulting in nephric inflammation, cell necrosis and dysfunction. Nucleic factor-kappa B was activated by TiO2 NPs exposure, promoting the expression levels of tumor necrosis factor-alpha, macrophage migration inhibitory factor, interleukin-2, interleukin-4, interleukin-6, interleukin-8, interleukin-10, interleukin-18, interleukin-1 beta, cross-reaction protein, transforming growth factor-beta, interferon-gamma and CYP1A1, while heat shock protein 70 expression was inhibited. These findings implied that TiO2 NPs-induced nephric injury of mice might be associated with alteration of inflammatory cytokine expression and reduction of detoxification of TiO2 NPs. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.
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