Neurotoxicological effects and the impairment of spatial recognition memory in mice caused by exposure to TiO2 nanoparticles.

Titanium dioxide nanoparticles (TiO(2) NPs) are now in daily use including popular sunscreens, toothpastes, and cosmetics. However, the effects of TiO(2) NPs on human body, especially on the central nervous system, are still unclear. The aim of this study was to determine whether TiO(2) NPs exposure results in persistent alternations in nervous system function. ICR mice were exposed to TiO(2) NPs through intragastric administration at 0, 5, 10 and 50 mg/kg body weight every day for 60 days. The Y-maze test showed that TiO(2) NPs exposure could significantly impair the behaviors of spatial recognition memory. To fully investigate the neurotoxicological consequence of TiO(2) NPs exposure, brain elements and neurochemicals were also investigated. The contents of Ca, Mg, Na, K, Fe and Zn in brain were significantly altered after TiO(2) NPs exposure. Moreover, TiO(2) NPs significantly inhibited the activities of Na(+)/K(+)-ATPase, Ca(2+)-ATPase, Ca(2+)/Mg(2+)-ATPase, acetylcholine esterase, and nitric oxide synthase; the function of the central cholinergic system was also noticeably disturbed and the contents of some monoamines neurotransmitters such as norepinephrine, dopamine and its metabolite 3, 4-dihydroxyphenylacetic acid, 5-hydroxytryptamine and its metabolite 5-hydroxyindoleacetic acid were significantly decreased, while the contents of acetylcholine, glutamate, and nitric oxide were significantly increased. These first findings indicated that exposure to TiO(2) NPs could possibly impair the spatial recognition memory ability, and this deficit may be possibly attributed to the disturbance of the homeostasis of trace elements, enzymes and neurotransmitter systems in the mouse brain. Therefore, the application of TiO(2) NPs and exposure effects especially on human brain for long-term and low-dose treatment should be cautious.

[1]  S. Yu Na(+), K(+)-ATPase: the new face of an old player in pathogenesis and apoptotic/hybrid cell death. , 2003, Biochemical pharmacology.

[2]  Navid B. Saleh,et al.  Titanium dioxide (P25) produces reactive oxygen species in immortalized brain microglia (BV2): implications for nanoparticle neurotoxicity. , 2006, Environmental science & technology.

[3]  Tao Zhang,et al.  Influences of nanoparticle zinc oxide on acutely isolated rat hippocampal CA3 pyramidal neurons. , 2009, Neurotoxicology.

[4]  Wei Liu,et al.  Toxicity and penetration of TiO2 nanoparticles in hairless mice and porcine skin after subchronic dermal exposure. , 2009, Toxicology letters.

[5]  M. Diers,et al.  Learning and memory impairment in adult rats due to severe zinc deficiency during lactation , 1983, Physiology & Behavior.

[6]  Z. Chai,et al.  Acute toxicity and biodistribution of different sized titanium dioxide particles in mice after oral administration. , 2007, Toxicology letters.

[7]  B. Vallee,et al.  The biochemical basis of zinc physiology. , 1993, Physiological reviews.

[8]  G. Gibson,et al.  Impaired Synthesis of Acetylcholine by Mild Hypoxic Hypoxia or Nitrous Oxide , 1981, Journal of neurochemistry.

[9]  E. Park,et al.  Nanosized titanium dioxide enhanced inflammatory responses in the septic brain of mouse , 2010, Neuroscience.

[10]  A. Lin Recovery by NO of the iron-attenuated dopamine dynamics in nigrostriatal system of rat brain , 1999, Neuroscience Research.

[11]  T. Shimazoe,et al.  Time-dependent effect of glutamate on long-term potentiation in the suprachiasmatic nucleus of rats. , 2002, Japanese journal of pharmacology.

[12]  Alberto E. Cassano,et al.  Air pollution remediation in a fixed bed photocatalytic reactor coated with TiO2 , 2005 .

[13]  J. Meek,et al.  Acetylcholine and Choline in Neuronal Tissue Measured by HPLC with Electrochemical Detection , 1983, Journal of neurochemistry.

[14]  M. Fei,et al.  Spleen injury and apoptotic pathway in mice caused by titanium dioxide nanoparticules. , 2010, Toxicology letters.

[15]  I. Silver,et al.  ATP and Brain Function , 1989, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  F. Hong,et al.  Biochemical Toxicity of Nano-anatase TiO2 Particles in Mice , 2008, Biological Trace Element Research.

[17]  F. Afaq,et al.  Cytotoxicity, pro‐oxidant effects and antioxidant depletion in rat lung alveolar macrophages exposed to ultrafine titanium dioxide , 1998, Journal of applied toxicology : JAT.

[18]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[19]  H. Simon,et al.  Deficits in spatial-memory tasks following lesions of septal dopaminergic terminals in the rat , 1986, Behavioural Brain Research.

[20]  A. Crane,et al.  Differential effects of electrical stimulation of sciatic nerve on metabolic activity in spinal cord and dorsal root ganglion in the rat. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[21]  J. Buccafusco,et al.  Multiple central nervous system targets for eliciting beneficial effects on memory and cognition. , 2000, The Journal of pharmacology and experimental therapeutics.

[22]  H. Prast,et al.  Nitric oxide as modulator of neuronal function , 2001, Progress in Neurobiology.

[23]  J. Bruni Ependymal development, proliferation, and functions: A review , 1998, Microscopy research and technique.

[24]  Guping Tang,et al.  In vivo acute toxicity of titanium dioxide nanoparticles to mice after intraperitioneal injection , 2009, Journal of applied toxicology : JAT.

[25]  Wilson F. Jardim,et al.  Remediation of pesticide contaminated soil using TiO2 mediated by solar light , 2002 .

[26]  E. Baulieu,et al.  The synthetic enantiomer of pregnenolone sulfate is very active on memory in rats and mice, even more so than its physiological neurosteroid counterpart: Distinct mechanisms? , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[27]  F. Hong,et al.  Toxicity of nano-anatase TiO2 to mice: Liver injury, oxidative stress , 2010 .

[28]  Jie Liu,et al.  Oxidative stress in the brain of mice caused by translocated nanoparticulate TiO2 delivered to the abdominal cavity. , 2010, Biomaterials.

[29]  C. Hölscher Nitric oxide, the enigmatic neuronal messenger: its role in synaptic plasticity , 1997, Trends in Neurosciences.

[30]  F. Hong,et al.  The Acute Liver Injury in Mice Caused by Nano-Anatase TiO2 , 2009, Nanoscale research letters.

[31]  D L Price,et al.  Alzheimer's disease: a disorder of cortical cholinergic innervation. , 1983, Science.

[32]  Z. Premji,et al.  Iron-Deficiency Anemia : Reexamining the Nature and Magnitude of the Public Health Problem An Analysis of Anemia and Child Mortality 1 , 2 , 2001 .

[33]  Kota Kobayashi,et al.  Optical characteristics of titanium oxide interference film and the film laminated with oxides and their applications for cosmetics. , 2004, Journal of cosmetic science.

[34]  Meng Wang,et al.  Neurotoxicity of low-dose repeatedly intranasal instillation of nano- and submicron-sized ferric oxide particles in mice , 2009 .

[35]  Wei Li,et al.  Potential neurological lesion after nasal instillation of TiO(2) nanoparticles in the anatase and rutile crystal phases. , 2008, Toxicology letters.

[36]  Wei Li,et al.  Time-dependent translocation and potential impairment on central nervous system by intranasally instilled TiO(2) nanoparticles. , 2008, Toxicology.

[37]  Shoji Okada,et al.  Brain uptake of trace metals, zinc and manganese, in rats , 1994, Brain Research.

[38]  M. Denny,et al.  Zinc deficiency and behavior: A developmental perspective , 1982, Physiology & Behavior.

[39]  R. Delorenzo,et al.  Neuronal-specific endoplasmic reticulum Mg(2+)/Ca(2+) ATPase Ca(2+) sequestration in mixed primary hippocampal culture homogenates. , 2004, Analytical biochemistry.

[40]  Ping Yang,et al.  Titanium dioxide nanoparticles co-doped with Fe3+ and Eu3+ ions for photocatalysis , 2002 .

[41]  R. Wolf,et al.  Sunscreens--the ultimate cosmetic. , 2003, Acta dermatovenerologica Croatica : ADC.

[42]  F. Hong,et al.  P38-Nrf-2 Signaling Pathway of Oxidative Stress in Mice Caused by Nanoparticulate TiO2 , 2011, Biological Trace Element Research.

[43]  T. Albanis,et al.  TiO2-assisted photocatalytic degradation of azo dyes in aqueous solution: kinetic and mechanistic investigations A review , 2004 .

[44]  G. Koob,et al.  Genetic Differences in Response to Novelty and Spatial Memory Using a Two-Trial Recognition Task in Mice , 2000, Neurobiology of Learning and Memory.

[45]  Richard D Handy,et al.  Toxicity of titanium dioxide nanoparticles to rainbow trout (Oncorhynchus mykiss): gill injury, oxidative stress, and other physiological effects. , 2007, Aquatic toxicology.

[46]  Navid B. Saleh,et al.  Nanosize Titanium Dioxide Stimulates Reactive Oxygen Species in Brain Microglia and Damages Neurons in Vitro , 2007, Environmental health perspectives.

[47]  Z. Chai,et al.  Distribution of TiO2 particles in the olfactory bulb of mice after nasal inhalation using microbeam SRXRF mapping techniques , 2007 .

[48]  T. Webb,et al.  Pulmonary toxicity study in rats with three forms of ultrafine-TiO2 particles: differential responses related to surface properties. , 2007, Toxicology.

[49]  A R Green,et al.  Iron deficiency and neurotransmitter synthesis and function , 1978, Proceedings of the Nutrition Society.

[50]  Saber M Hussain,et al.  The interaction of manganese nanoparticles with PC-12 cells induces dopamine depletion. , 2006, Toxicological sciences : an official journal of the Society of Toxicology.

[51]  J. Verran,et al.  Photocatalytic Coatings for Environmental Applications† , 2005, Photochemistry and photobiology.