Titanium dioxide nanoparticles decreases activity of rat brain when administered prenatally
DOI:
https://doi.org/10.18203/2319-2003.ijbcp20161510Keywords:
Conditioned avoidance response, Brain damage, Neurotoxicity, Nanoparticles, NeurogenesisAbstract
Background: Titanium dioxide nanoparticles are widely used in the sunscreens, toothpastes, and cosmetic products that the human use daily. Previous reports have proved that the impact of nanomaterials on brain activity is not negligible, especially for the people working in nanomaterials manufacturing factories. We are using titanium dioxide in our daily life in cosmetics, food industry and many other pharmaceutical products. So to keep a check on the threat what these chemicals may cause, we conducted a research to study effect of titanium dioxide nanoparticles on rat brain. This research gave us an insight of the possible threats it can cause to brain.
Methods: The effects of titanium dioxide nanoparticles on brain activity were reported. Our studies showed that titanium dioxide nanoparticles have a differential tendency towards neurons. To insight the possible effect on titanium dioxide nanoparticles on neurobehaviour we conducted a conditioned avoidance response study using shuttle box analysis. In the study we administered the drug titanium dioxide nanoparticles prenatally and observed its effects by neurobehaviour studies in progenies of wistar rat.
Results: In the results we observed that titanium dioxide nanoparticles have caused a decreased learning and memory behaviours as compared to control groups.
Conclusions: We studied the neurobehaviour of progenies, when the drug was administered to rat brain prenatally. The results showed that the titanium dioxide nanoparticles particles have decreased the brain activity of the rat brain by showing decreased brain activity in progenies also.
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References
Yuguan Z, Sheng L, Zhao X, Hong J. Titanium dioxide nanoparticles nanoparticles induced hippocampal neuroinflammation in mice. PLoS One. 2014;9(3):e92230.
Nanotoxicology: Toxicological and Biological activities of nanomaterials, The Chinese academy of sciences. Available at http://www.eolss.net/sample-chapters/c05/e6-152-35-00.pdf. Accessed 12 December 2015.
Kreyling WG, Semmler M, Erbe F, Mayer P, Takenaka S, Schulz H, et al, Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low. J Toxicol Environ Health A. 2002;65(20):1513-30.
Takenaka S, Karg E, Roth C, Schulz H, Ziesenis A, Heinzmann U, et al. Pulmonary and systemic distribution of inhaled ultrafine silver particles in rats. Environ Health Perspect. 2001;109:547-51.
Adams LK, Lyon DY, Mcintosh A, Alvarez PJ. Comparative toxicity of nano-scale Titanium dioxide nanoparticles, SiO2 and ZnO water suspensions. Water Sci Technol. 2006;54:327-34.
Zhang L, Bai R, Li B, Ge C, Du J, Liu Y,et al Rutile titanium dioxide nanoparticles particles exert size and surface coating dependent retention and lesions on the murine brain. Toxicol Lett. 2011;207(1):73-81.
Shwe TTW, Fujimaki H. Nanoparticles and Neurotoxicity. Int J Mol Sci. 2011;12(9):6267-80.
Kaida T, Kobayashi K, Adachi M, Suzuki F. Optical characteristics of titanium oxide interference film and the film laminated with oxides and their applications for cosmetics. Cosmet Sci. 2004;55:219-20.
Choi H, Stathatos E, Dionysiou DD. Sol-gel preparation of meso porous photocatalytic titanium dioxide nanoparticles films and titanium dioxide nanoparticles/Al2O3 composite membranes for environmental applications. Appl Catal B-Environ.2006;63:60-7
Fisher J, Egerton T. Titanium compounds, inorganic: Kirk-Othmer Encyclopedia of Chemical Technology. New York: John Wiley and Sons; 2001.
Kreyling WG, Semmler M, Erbe F, Mayer P, Takenaka S, Schulz H, et al. Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low. J Toxicol Environ Health A. 2002;65:1513-30.
Sager TM, Kommineni C, Castranova V. Pulmonary response to intratracheal instillation of ultrafine versus fine titanium dioxide: role of particle surface area. Particle and Fibre Toxicology. 2008;5:17.
Long TC, Saleh N, Tilton RD, Lowry VG, Veronesi B. Titanium dioxide (P25) produces reactive oxygen species in immortalized brain microglia (BV2): implications for nanoparticle neurotoxicity. Environ Sci Technol. 2006;40(14):4346-52.
Trouiller B, Reliene R, Westbrook A, Solaimani P, Robert H. Schiest L, Titanium dioxide nanoparticles induce DNA damage and genetic instability in-vivo in mice. American Association for cancer research. Cancer Res. 2009;69:22.
Chen Y, Azad MB, Gibson SB. Super oxide is the major reactive oxygen species regulating autophagy.Cell Death Diff. 2009;16:1040-52.
Gage FH. Neurogenesis in the Adult Brain, California. The Journal of Neuroscience. 2002;22(3):612-3.
Doetsch F, Caille I, Lim DA, Garcia-Verdugo JM, Alvarez BA. Subventricular zone astrocytes are neural stem cells in the adult mammalian brain. Cell. 1999;97,703-16.
Eriksson PS, Perfilieva E, Eriksson TB, Alborn AM, Nordborg C, Daniel A, et al. Neurogenesis in the adult human hippocampus. Nature Medicine. 1998;4:1313-7.
Johansson C, Deveney AM, Reif D, Jackson DM. The neuronal selective nitric oxide inhibitor AR-R 17477, blocks some effects of phencyclidine, while having no observable behavioural effects when given alone. Pharmacol Toxicol. 1999;84:226-33.
Cameron HA, Mckay RD. Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus. J Comp Neurol. 2001;435(4):406-17.
Praag HV, Alejandro F, Schinder, Brian R, Christie, Toni N, et al. Functional neurogenesis in the adult hippocampus.Nature. 2002;415:1030-4.
Harry GJ, Billingsley M, Bruinink A, Campbell IL, Classen W, Dorman DC, et al. In-vitro techniques for the assessment of neurotoxicity. Environ Health Perspect. 1998;106(1):131-58.
Chen Y, Garcia GE, Huang W, Shlomi C. The involvement of secondary neuronal damage in the development of neuropsychiatric disorders following brain insults. Front Neurol. 2014;5:22-4.
Sayes CM, Wahi R, Kurian PA, Liu Y, West JL, Ausman KD, et al. Correlating nanoscale titania structure with toxicity: a cytotoxicity and inflammatory response study with human dermal fibroblasts and human lung epithelial cells. Toxicol Sci. 2006;92:174-85.
Nanomaterial Case Studies: Nanoscale Titanium Dioxide in Water Treatment and in Topical Sunscreen. Available at https://cfpub.epa.gov /ncea/risk/ recordisplay.cfm?deid. Accessed 18 December 2015.
Lorenz C, Tiede K, Tear S, Boxall A, Goetz N, Hungerbuhler K. Imaging and characterization of engineered nanoparticles in sunscreens by electron microscopy, under wet and dry conditions. International Journal of Occupational Environmental Health. 2010;16(4):406-28.
Kowalkowskia T, Buszewskia B, Cantadob C, Dondib F. Field-flow fractionation: Theory, techniques, applications and the challenges. Critical Reviews in Analytical Chemistry. 2006;36(2):129-35.
Adams LK, Lyon DY, Mcintosh A, Alvarez PJ. Comparative toxicity of nano-scale titanium dioxide nanoparticles, SiO2 and ZnO water suspensions. Water Sci Technol. 2006;54:327-34.
Luan J, Wang S, Hu Z, Zhang L. Synthesis techniques, properties and applications of polymer nanocomposites. Curr Org Synth. 2012;9:114-36.
Roy SC, Paulose M, Grimes CA. The effect of titanium dioxide nanoparticles nanotubes in the enhancement of blood clotting for the control of hemorrhage. Biomaterials. 2007;28(31):4667-72.
Liu L, Miao P, Xu Y, Tian Z, Zou Z, Li G. Study of Pt/Titanium dioxide nanoparticles nanocomposite for cancer-cell treatment. J Photochem Photobiol B. 2010;98(3):207-10.
Lockman PR, Koziara JM, Mumper RJ, Allen DD. Nanoparticle surface charges alter blood–brain barrier integrity and permeability. Journal of Drug Targeting. 2004;12:635-41.
Kreyling WG, Semmler M, Erbe F, Mayer P, Takenaka S, Schulz H, Oberdorster G, Ziesenis A. Translocation of ultrafine insoluble iridium particles from lung epithelium to extrapulmonary organs is size dependent but very low. Journal of Toxicology and Environmental Health Part A.2002;65:1513-30.
Oberdorster G, Sharp Z, Atudorei V, Elder A, Gelein R, Kreyling W, Cox C. Translocation of inhaled ultrafine particles to the brain. Inhalation Toxicology. 2004;16:437-45.
Curwin B, Bertke S, Exposure characterization of metal oxide nanoparticles in the workplace. J Occup Environ Hyg. 2011;8(10):580-7.
Lee YS, Kim DW, Lee YH, Oh JH, Yoon S, Choi MS, et al. Silver nanoparticles induce apoptosis and G2/Marrest via PKCf-dependent signaling in A549 lung cells. Arch Toxicol. 2011;85:1529-40.
Moreira KM, Hipolide DC, Nobrega JN, Bueno OF, Tufik S, Oliveira MG. Deficits in avoidance responding after paradoxical sleep deprivation are not associated with altered [3H] pirenzepine binding to M1 muscarinic receptors in rat brain. Brain Res. 2002;977:31-7.
Liu R, Yin L, Pu Y, Liang G, Zhang J, Su J, et al. Pulmonary toxicity induced by three forms of titanium dioxide nanoparticles via intra- tracheal instillation in rats, Progress in Natural Science. 2009;19:573-79.
Rollerova E, Tulinska J, Liskova A, Kuricova M, Kovriznych J, Mlynarcikova A, Kiss A, Scsukova S. Titanium dioxide nanoparticles: some aspects of toxicity/focus on the development, Endocrine Regulations. 2015;49:97-112.