Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: KEGG:D01931 (TiO2)
 11,320 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Steady-state mRNA levels and immunoreactive protein for manganese-containing superoxide dismutase (MnSOD) were assayed in rat lungs after subchronic inhalation of the fibrogenic silicon dioxide, cristobalite, or preparations of titanium dioxide (TiO2) of different inflammatory and fibrogenic potential. Total and differential cell counts recoverable by bronchoalveolar lavage (BAL) were also measured to ascertain whether induction of certain antioxidant enzymes (AOE) correlated with inflammatory responses. Inhalation of cristobalite and ultra-fine TiO2, a particle causing pulmonary inflammation and fibrosis, caused dramatic increases in MnSOD mRNA levels in rat lung which correlated with increases in MnSOD immunoreactive protein. Increases in gene expression of other AOE [catalase, glutathione peroxidase (GPX), copper-zinc containing superoxide dismutase (CuZnSOD)] were less striking and did not correlate precisely with inflammatory potential of minerals. Inflammatory changes in BAL correlated directly with steady-state MnSOD mRNA levels in lung. Inhalation of TiO2-F, a noninflammatory, nonfibrogenic mineral, failed to induce MnSOD or mRNAs for other AOE. Our data suggest that particles causing inflammation and pulmonary fibrosis increase expression of AOE in lung, most notably MnSOD. Thus, elevations of MnSOD mRNA levels in lung or BAL may be predictive of lung disease.
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PMID:Increased expression of manganese-containing superoxide dismutase in rat lungs after inhalation of inflammatory and fibrogenic minerals. 806 94

Using TiO2 photocatalyst, arsenite [As(III)] can be rapidly oxidized to arsenate [As(V)], which is less toxic and less mobile in the aquatic environment. Superoxides have been recently proposed as a main photocatalytic oxidant of As(III) whereas OH radicals are dominant oxidants in most TiO2 photocatalytic oxidation (PCO) reactions. This study confirms that superoxides are mainly responsible for the As(III) PCO by investigating PCO kinetics in pure and modified TiO2 systems. The rate of As(III) oxidation drastically increased on Pt-TiO2, which could be ascribed to the enhanced superoxide generation through an efficient interfacial electron transfer from the conduction band (CB) to O2. Since the addition of tert-butyl alcohol (OH radical scavenger) had little effect on the PCO rate in both naked and Pt-TiO2 suspensions, OH radicals do not seem to be involved. The addition of polyoxometalates (POMs) as an electron shuttle between TiO2 CB and 02 highly promoted the PCO rate whereas the POM alone was not effective at all in oxidizing As(III). Fluorinated TiO2 that had a markedly reduced adsorptive capacity for As(III) did not show a reduced PCO rate, which indicates that the direct hole transfer path is not important. The arsenite oxidation proceeded under visible light with a similar rate to the case of Pt-TiO2/UV when dye-sensitized Pt-TiO2 was used. Since only superoxides can be generated as a photooxidant in this visible light system, their role as a main oxidant of As(III) is confirmed. In addition, the PCO rate was significantly reduced in the presence of superoxide dismutase.
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PMID:Effects of TiO2 surface modifications on photocatalytic oxidation of arsenite: the role of superoxides. 1521 69

Oxidation of arsenite, As(III), to arsenate, As(V), is required for the efficient removal of arsenic by many water treatment technologies. The photocatalyzed oxidation of As(III) on titanium dioxide, TiO2, offers an environmentally benign method for this unit operation. In this study, we explore the efficacy and mechanism of TiO2-photocatalyzed As(III) oxidation at circumneutral pH and over a range of As(III) concentrations approaching those typically encountered in water treatment systems. We focus on the effect of As adsorption on observed rates of photooxidation. Adsorption (in the dark) of both As(III) and As(V) on Degussa P25 TiO2 was examined at pH 6.3 over a range in dissolved arsenic concentrations, [As]diss, of 0.10-89 microM and 0.2 or 0.05 g L(-1) TiO2 for As(III) and As(V), respectively. Adsorption isotherms generally followed the Langmuir-Hinshelwood model with As(III) exhibiting an adsorption maxima of 32 micromol g(-1). As(V) adsorption did not reach a plateau under the experimental conditions examined; the maximum adsorbed concentration observed was 130 micromol g(-1). The extent of As(III) and As(V) adsorption observed at the beginning and end of the kinetic studies was consistent with that observed in the adsorption isotherms. Kinetic studies were performed in batch systems at pH 6.3 with 0.8-42 microM As(III) and 0.05 g L(-1) TiO2; complete oxidation of As(III) was observed within 10-60 min of irradiation at 365 nm. The observed effect of As(III) concentration on reaction kinetics was consistent with surface saturation at higher concentrations. Addition of phosphate at 0.5-10 microM had little effect on either As(III) sorption or its photooxidation rate but did inhibit adsorption of the product As(V). The selective use of hydroxyl radical quenchers and superoxide dismutase demonstrated that superoxide, O2-, plays a major role in the oxidation of As(III) to As(V).
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PMID:TiO2-photocatalyzed As(II) oxidation in aqueous suspensions: reaction kinetics and effects of adsorption. 1581 51

The effects of nano-TiO2 (rutile) on the chloroplast aging of spinach under light were studied. The results showed that when the chloroplasts were illuminated for 1, 5, and 10 min with 500 micromol/cm2/min light intensity, respectively, the evolution oxygen rate was rapidly increased; when the chloroplasts were treated for 20, 30, and 40 min with 500 micromol/cm2/min light intensity, respectively, the evolution oxygen rate was gradually decreased. While spinach was treated with 0.25% nano-TiO2, the rate of evolution oxygen of chloroplasts in different illumination times (1, 5, 10, 20, 30, and 40 min) was higher than that of control, and when the illumination time was over 10 min, the reduction of the evolution oxygen rate was lower than that of control. It suggested that nano-TiO2 treatment could protect chloroplasts from aging for long-time illumination. The mechanism researches indicated that nano-TiO2 treatment could significantly increase the activities of superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD), decrease accumulation of reactive oxygen free radicals and the level of malondialdehyde (MDA), and maintain stability of membrane structure of chloroplast under light.
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PMID:Influences of nano-TiO2 on the chloroplast aging of spinach under light. 1593 May 94

Sunscreens protect skin against sunburn. However, studies have demonstrated that UV-irradiated sunscreen components such as titanium dioxide (TiO2) promote the photogeneration of reactive oxygen species (ROS). Because encapsulation of TiO2 within zeolites alters its photocatalytic activity, supramolecular composites based on NaY zeolite hosts containing TiO2 guests were prepared, and the effects on ROS formation in cells under UVA-irradiation evaluated. DCFH-DA (2',7'-dichlorofluorescein diacetate) was used as a profluorescent probe to monitor intracellular ROS. The detection of intracellular 2',7'-dichlorofluorescein (DCF) fluorescence by confocal microscopy revealed that DCFH-DA was taken up, hydrolyzed and oxidized by yeast cells and cultured human skin fibroblasts within 20 and 6 min, respectively. Higher DCF fluorescence was observed in fibroblasts following UVA irradiation in the absence but not in the presence of the radical nitroxide, TEMPOL (4-hydroxy-2,2,6,6-tetramethylpiperydine-1-oxyl), which exhibits superoxide dismutase-mimetic and catalase-mimetic activity. UVA-induced fluorescence increased by approximately 50% in the presence of 32-nm anatase TiO2 particles and decreased by essentially an equal amount in the presence of TiO2 encapsulated within NaY zeolites (TiO2@NaY). Addition of the uncomplexed NaY host also decreased (by approximately 30%) the amount of UVA-induced fluorescence but, unexpectedly, the combination of the free guest and host (TiO2+NaY) caused a doubling of the fluorescence. Protection of cells against TiO2-induced intracellular ROS by encapsulation suggests that supramolecular species may be beneficial in photoprotection of the skin. In contrast, the potentiation of TiO2-induced ROS by uncomplexed NaY points to a critical role for formulation when free TiO2 is used as a sun screen ingredient.
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PMID:Zeolite encapsulation decreases TiO2-photosensitized ROS generation in cultured human skin fibroblasts. 1614 47

The adverse effect of Ti on body-defense macrophage is not well understood. The aims of this study were twofold: (1) to examine the intracellular accumulation of Ti element; and (2) to measure the cell viability, superoxide dismutase (SOD) production, and TNF-alpha secretion of macrophage-like RAW264 cells cultured for two days in medium with 1 ppm Ti prepared from acidic ICP Ti standard solution. PIXE analysis showed that element Ti was accumulated up to 7.3 ppm in RAW264 cells when cultured in the medium with 1 ppm Ti. Further, RAW264 cells cultured in the medium with 1 ppm Ti exhibited cell viability of about 60%, SOD production of about 180%, and TNF-alpha secretion of about 170% relative to those of control cells cultured in the medium without Ti. It was speculated that phagocytosis of minute Ti-containing complex (mostly TiO2) by macrophage caused oxidative stress and inflammatory reaction, leading to cell proliferation arrest and increased production of SOD and TNF-alpha.
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PMID:Accumulation of element Ti in macrophage-like RAW264 cells cultured in medium with 1 ppm Ti and effects on cell viability, SOD production and TNF-alpha secretion. 1733 7

Titanium dioxide (TiO2) is extensively used in many industrial areas, including cosmetics, pharmaceutical, paint and paper production. Although the uses of TiO2 have become so widespread, there is limited information concerning its toxicity on humans. However, the genotoxicity of TiO2 remains to be controversial. The possible genotoxic effects of TiO2 have been evaluated in human whole blood cultures (WBCs) related to oxidative status. The blood was processed to examine the following oxidative stress markers: glutathione peroxidase, glutathione reductase, superoxide dismutase and catalase. In addition, the frequencies of sister-chromatid exchanges (SCEs) and micronuclei (MN) were scored as genetic endpoints. Different concentrations of TiO2 (1, 2, 3, 5, 7.5 and 10 microM) were tested. From the results, it appeared that TiO2 was able to induce genotoxic effects, as observed by the increases found in SCE and MN frequencies in TiO2-treated cultures. Present results also show that treatments with TiO2 promoted oxidative stress in human WBC with an increase in concentrations. In conclusion, our data indicate that TiO2 can enhance oxidative stress-mediated DNA damage in vitro.
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PMID:An in vitro blood culture for evaluating the genotoxicity of titanium dioxide: the responses of antioxidant enzymes. 1772 36

Nanotitanium dioxide (TiO2) is an important industrial material that is widely used as an additive in cosmetics, pharmaceuticals, and food colorants. Although the small size of the TiO2 nanoparticle is useful in various applications, the biosafety of this material needs to be evaluated. In this study, mouse fibroblast (L929) cells were used to evaluate the cytotoxicity of different concentrations (3-600 microg/mL) of homogeneous and weakly aggregated TiO2 nanoparticles in aqueous solution. The L929 cells became round and even shrank as the concentration of TiO2 nanoparticles increased. Moreover, TiO2 nanoparticle-treated cells had condensed fragmented chromatin or were directly necrosed, as observed by acridine orange (AO) staining. The transmission electron microscopy (TEM) analysis showed that in cells cultured in a medium containing 300 microg/mL TiO2, the number of lysosomes increased, and some cytoplasmic organelles were damaged. In addition, there was a significant increase in oxidative stress at higher TiO2 nanoparticle concentrations (>60 microg/mL). As the concentration of TiO2 nanoparticles increased in the culture medium, the levels of reactive oxygen species (ROS) and lactate dehydrogenase (LDH) increased, while those of methyl tetrazolium cytotoxicity (MTT), glutathione (GSH), and superoxide dismutase (SOD) decreased. A possible mechanism for the cytotoxicity of TiO2 nanoparticles is also discussed.
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PMID:Cytotoxicity of titanium dioxide nanoparticles in mouse fibroblast cells. 1868 Mar 14

Active oxygen species generated by photoexcitation of TiO2 sol solutions were directly observed by the single-shot near-field heterodyne transient grating method. Transient responses were compared in the presence and absence of various kinds of scavengers such as sodium azide, dimethyl sulfoxide, and superoxide dismutase, and three components of the transient responses were assigned to hydroxyl radicals, hydrogen peroxide, and superoxide radicals. The diffusion coefficients of each active oxygen species were obtained by the analysis of the transient responses, and it was revealed that they were 1-3 orders smaller than those for molecules with a similar size. It was proposed that this is because the active oxygen species are under equilibrium between free radicals and adsorbed species on a TiO2 surface. Furthermore, it was suggested that the adsorption equilibrium for each species was varied depending on the pH of the solutions.
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PMID:Lifetime and diffusion coefficient of active oxygen species generated in TiO2 sol solutions. 1930 3

Nano-TiO2 and superoxide dismutase (SOD, EC 1.15.1.1) have been added to cosmetics and used to prevent injury of skin from UV-radiation, which might be related to the decrease of oxidative damage of skin. In previous studies we had proven that nano-anatase could increase the activity of SOD and decrease the oxidative damage in vivo. The mechanisms by which nano-anatase promoted SOD activity, however, are still not clearly understood. In the present work, nano-anatase in various concentrations was added to SOD from rat erythrocytes in vitro to gain insight into the mechanism of molecular interactions between nano-anatase and SOD by various spectral methods, suggesting that the reaction between SOD and nano-anatase was two-order, which meant that the SOD activity was greatly increased by low concentration of nano-anatase and inhibited by high concentration of nano-anatase. The spectroscopic assays suggested that the nano-anatase was determined to directly bind to SOD; the binding site of nano-anatase to SOD was 0.256 and the binding constants were 6.54 x 10(5) and 3.6 x 10(5)Lmol(-1); Ti was bound with three oxygen or nitrogen atoms and a sulfur atoms of amino acid residues at the Ti-O(N) and Ti-S bond lengths of 1.86 and 2.37 A, respectively, the binding nano-anatase entirely altered the secondary structure of SOD. It implied that the nano-anatase coordination created a new metal ion-active site form in SOD, thus leading to an enhancement in SOD activity.
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PMID:Direct evidence for interaction between nano-anatase and superoxide dismutase from rat erythrocytes. 1934 6


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