PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “MAGNESIUM OXIDE”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 523 records · Page 29Linked to original sources
PubMed2002

Lead adsorption to metal oxides and organic material of freshwater surface coatings determined using a novel selective extraction method.

Surface coatings were collected in three lakes and a river in China to study the role of the components of natural surface coatings in controlling Pb adsorption. Chemical reagents, 0.02 mol/l NH2OH HCl+0.01 mol/l HNO3, 0.4 mol/l Na2S2O4 and 10% oxalic acid, were employed to extract one or more components from surface coatings, and then Pb adsorption to extracted and unextracted surface coatings was carried out. The observed Pb adsorption to extracted and Unextracted surface coatings were analyzed using the nonlinear least squares fitting (NLSF) to estimate the relative contribution of components to the total Pb adsorption. The amounts of Pb absorption to components described by estimated gamma(max) ranged from 0.1126 to 0.7291 (mol Pb/mol Mn) for Mn, 0.0528 to 0.1927 (mol Pb/mol Fe) for Fe and 0.0196 to 0.1020 (mol Pb/kg COD) for organic material, respectively. In all waters studied, metal oxides contributed most to Pb adsorption with a lesser role indicated for organic material.

Adsorption↗
PubMed2005

Shading of ceramic crowns using digital tooth shade matching devices.

In the 1990s, there was great optimism due to the development of devices for measuring tooth shade. The frequently not so simple, visual determination of the shade of a tooth was to be done with the aid of a device which recognizes the shade and describes it accurately by reference to a color chart. However, the skepticism towards such devices was also great. It is known that the color effect frequently differs strongly when comparing a tooth from the shade guide with a metal ceramic crown, despite identical shade designation. Anyone who considers visual shade determination to be inadequate and places his hopes in digital shade matching devices will be disappointed. It is the shade-generating structures of the metal ceramic and frequently of the veneer layers that turn out to be too thin which, despite correct shade selection, cause a different color perception. Such problems have been reduced decisively with the development of fracture-proof hard porcelain caps (Vita In-Ceram) with optical characteristics similar to teeth. In addition, the Vita System 3D-Master tooth shade system developed in 1998 by Vita in cooperation with Dr. Hall from Australia, leads the practitioner to a better understanding of the primary tooth shade characteristics of "brightness (value)", "color intensity (chroma)" and "color (wave length of the visible light, hue)". These two innovations allow a more accurate estimate of the basic shade of a natural tooth (reference tooth) and the imitation in the laboratory of its natural, shade-generating structures. If digital shade measurement supplements the visual shade estimate, then a further improvement can be expected--especially in the recognition of the basic shade. Qualitative descriptions of subjective shade measurement of a natural tooth and of its imitation in the dental laboratory by ceramics can be found frequently in professional journals and publications. With digital tooth shade matching devices, which apart from the color code of the color chart also reproduce exact, colorimetric values, such work processes can be recorded quantitatively and objectively. Reports about this type of controlled shade determination and generation are found rarely in the literature, which is surprising in view of the large number of tooth shade matching devices and dental ceramic systems available. In the present paper, the influence of the individual ceramic layers on color perception is measured and described under standardized conditions. The creation of the basic shade as it results from the composition of the various ceramic layers is traced with a spectrophotometer. The Vita In-Ceram Alumina infiltration ceramic and the VitaVM7 veneer ceramic were selected as the ceramic system. MHT-SpectroShade and Vita Easyshade were used as shade matching devices.

Aluminum Oxide↗
PubMed1973

The effect of magnesium ions on the dimethylaniline oxidation rate and electron transfer in liver microsomal fraction.

1. Reactions of N-demethylation, p-hydroxylation and N-oxidation of one substrate, i.e. dimethylaniline, have been used to show that the activating effect of Mg(2+) takes place only in the first two reactions. 2. An increase in V(max.) of N-demethylation of dimethylaniline is accompanied by an increase in K(m). In the p-hydroxylation of dimethylaniline V(max.) increases whereas K(m) does not change. A comparison of the changes in the K(m) values of these reactions with the change in K(s) shows that in both cases K(m) does not characterize the affinity of cytochrome P-450 for dimethylaniline. 3. The rate-limiting site of N-demethylation and p-hydroxylation of dimethylaniline, as well as the total rate of NADPH oxidation in the presence of dimethylaniline, is between cytochromes b(5) and P-450. Addition of Mg(2+) to the incubation medium changes the hydrophobic environment of phosphatidylcholine in the membrane, the process being accompanied by a sharp increase in the fluorescence quantum yield of 8-anilinonaphthalene-1-sulphonate.

Aniline Compounds↗
PubMed2006

Oxidation of trichloroethene over metal oxide catalysts: kinetic studies and correlation with adsorption properties.

The performance of bulk chromium oxide is compared with that of a Mn commercial catalyst for the deep oxidation of trichloroethene (1000-2500ppmv, 55h(-1) space velocity) in air, in dry and wet (20000ppm of H(2)O) conditions, in terms of activity, selectivity and stability. Chromium oxide was found to be more active (on a catalyst weight basis), however its activity decreases continuously with time on stream. The presence of water increases its stability, the Mn catalyst showing the opposite behaviour. The effect of water on the Cr catalyst can be explained according to the Deacon equilibrium, as the presence of water tends to decrease the Cl(2) concentration, assumed to be responsible of the catalyst deactivation. Regarding to the selectivity, the Mn catalyst yields C(2)Cl(4), CCl(4) and CHCl(3) as organochlorinated by-products, whereas chromium oxide produces only trace amounts of CCl(4). Simple power-law kinetics expressions (first-order for Mn and zero-order for Cr) provide fairly good fits for the evolution of the conversion with the temperature. Furthermore, the kinetic behaviour of chromium oxide can be represented with a Langmuir-Hinshelwood model taking into account the chlorine inhibitory effect.

Adsorption↗
PubMed1993

Dysprosium as a nonabsorbable marker for studies of mineral absorption with stable isotope tracers in human subjects.

Two studies were conducted to determine if dysprosium (Dy) could be used as a quantitative fecal marker for studies of zinc-70 (70Zn), copper-65 (65Cu) and magnesium-26 (26Mg) absorption in humans. In the first experiment, Dy excretion was shown to be complete (104 +/- 9%; mean +/- SD, n = 6) and the kinetics of fecal Dy excretion closely paralleled that of 70Zn but not 65Cu. Because of the similarity in 70Zn and Dy excretion kinetics, a method for estimating 70Zn absorption was developed which used 70Zn and Dy data from only the first two stools passed after isotope administration. Average estimates of 70Zn absorption based on the two-stool (partial pool) vs total pool (5-day composite) method were not different (28.0 +/- 5.2 vs 24.4 +/- 4.1%, respectively; means +/- SEM; p > 0.10). In the second study, the same questions was addressed relative to 26Mg absorption. 26Mg and Dy also exhibited nearly identical excretion patterns. Average estimates of 26Mg absorption based on the partial pool vs total pool method were comparable yielding mean values of 22.7 +/- 3.4 vs 23.2 +/- 2.5% and 26.1 +/- 1.8 vs 24.3 +/- 1.8%, respectively, from magnesium-26 oxide (26MgO) and 26Mg glycinate. Advantages and limitations of the partial pool method for estimating mineral absorption are discussed.

Absorption↗
PubMed2004

Survival rate of mono-ceramic and ceramic-core CAD/CAM-generated anterior crowns over 2-5 years.

Anterior mono-ceramic (Mk II, n = 18) and ceramic core (In-Ceram Spinell, n = 18) crowns were CAD/CAM-fabricated using Vitablocs with the Cerec 2 CAD/CAM system and bonded in 24 patients. All crowns were rated using modified United States Public Health Services (USPHS) criteria at baseline and after a service time of 2-5 years. Survival of the crowns, regarding fracture, was analysed (Kaplan-Meier) after 44.7 +/- 10.3 months. Gingival health at crowns was assessed using plaque and bleeding scores. One core crown and one mono-ceramic crown had fractured after 42.5 months and 12 months, respectively, with survival rates of 91.7% for In-Ceram Spinell and 94.4% for Mk II; the difference was not statistically significant. Between baseline and follow-up examinations, non-significant shifts from A- to B-ratings occurred, particularly for marginal adaptation, for both crown types. Plaque and bleeding scores did not differ between the ceramic crown types but showed significantly less plaque and less bleeding at ceramic crowns than at control teeth at follow-up. The clinical performance of mono-ceramic crowns was judged to be similar to that of ceramic core crowns.

Adult↗
PubMed2002

Arsenic(III) oxidation by birnessite and precipitation of manganese(II) arsenate.

Solution chemical techniques were used to investigate the oxidation of As(III) to As(V) in 0.011 M arsenite suspension of well-crystallized hexagonal birnessite (H-birnessite, 2.7 g L(-1)) at pH 5. Products of the reaction were studied by scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS), atomic force microscopy (AFM), and X-ray absorption near-edge structure spectroscopy (XANES). In the initial stage (first 74 h), chemical results have been interpreted quantitatively, and the reaction is shown to proceed in two steps as suggested by previous authors: 2>Mn(IV)O2 + H3AsO3 + H2O --> 2>Mn(III)OOH + H2AsO4- + H+ and 2>Mn(III)OOH + H3AsO3 + 3H+ --> 2Mn2+ + H2AsO4- + 2H2O. The As(III) depletion rate was lower (0.02 h(-1)) than measured in previous studies because of the high crystallinity of the H-birnessite sample used in this study. The surface reaction sites are likely located on the edges of H-birnessite layers rather than on the basal planes. The ion activity product of Mn(II) and As(V) reached after 74 h reaction time was the solubility product of a protonated manganese arsenate, having a chemical composition close to that of krautite as identified by XANES and EDS. Krautite precipitation reaction can be written as follows: Mn2+ + H2AsO4- + H2O = MnHAsO4 x H2O + H+ log Ks approximately -0.2. Equilibrium was reached after 400 h. The manganese arsenate precipitate formed long fibers that aggregated at the surface of H-birnessite. The oxidation reaction transforms a toxic species, As(III), to a less toxic aqueous species, which further precipitates with Mn2+ as a mixed As-Mn solid characterized by a low solubility product.

Arsenates↗
PubMed2002

[Protective effect of magnesium on the damaged cultured endothelial cells induced by oxidized low density lipoprotein].

The protective effect of magnesium on endothelial cells induced by H2O2 and t-butyl hydroperoxide and the subsequent alterations of extracellular superoxide dismutase (EC-SOD) and cellular selenium-dependent and non-selenium-dependent GSH-Px are investigated in this study. Low density lipoproteins (LDLs) are isolated from poeled healthy human fresh sera by ultracentrifugation. Conjugate diene was measured for assessing the susceptibility of LDL to oxidation mediated by Cu2+. The extent of LDL modification is determined by measuring the formation of thiobarbituric acid reaction substances (TBARS). In addition, human umbilical vein endothelial cells are used to assess the effect of magnesium on damage induced by oxidized LDL (ox-LDL). The extent of cellular lipid peroxides is determined by measuring the formation of TBARS. Results show that (1) the presence of Mg2+ resulted in a protracted lag phase at doses of 0.3, 0.6, 1.2 and 2.4 mmol/L, as well as the presence of Mg2+ at doses of 0.3 and 0.6 mmol/L decreases the production of TBARS when LDL is oxidized by the addition of Cu2+; (2) the formation of TBARS is significantly reduced in the group of ox-LDL + Mg2+ at doses of 0.3, 0.6, 1.2 and 2.4 mmol/L. The activity of EC-SOD, GSH-Px with and without selenium in the group of ox-LDL + Mg2+ at all doses increases significantly compared with ox-LDL group. It is concluded that magnesium inhibits LDL oxidation mediated by Cu2+ and protected endothelial cells from lipid peroxidation and reinforces the activities of antioxidant enzymes.

Cells, Cultured↗
PubMed2000

Human placenta sphingomyelinase, an exogenous acidic pH-optimum sphingomyelinase, induces oxidative stress, glutathione depletion, and apoptosis in rat hepatocytes.

Ceramide has been identified as a putative lipid messenger that mediates diverse cellular processes including cell death. Since glutathione (GSH) depletion is known to sensitize cells to many cytotoxic agents and as a result of the reported regulation of neutral sphyngomyelinase (NSMase) by GSH, the present study compared the role of individual SMases in the induction of oxidative stress, regulation of cellular GSH, and apoptosis of rat hepatocytes. Exposure of cultured rat hepatocytes to exogenous Bacillus cereus sphingomyelinase (bSMase), a neutral SMase, or human placenta sphingomyelinase (hSMase), an acidic SMase (ASMase), generated similar ceramide levels in a dose-dependent manner. However, whereas bSMase increased hepatocellular GSH levels, hSMase depleted GSH stores, an effect that was prevented by monensin and mannose 6-phosphate (M-6-P), suggesting that exogenous hSMase enters hepatocytes by endocytosis and is delivered to an endosomal/lysosomal acidic compartment. Interestingly, despite the differential effect of either SMases on cell GSH levels, both bSMase and hSMase increased gamma-glutamylcysteine synthetase heavy-subunit chain (gamma-GCS-HS) mRNA levels. Consistent with these findings on GSH regulation, hSMase, but not bSMase, generated reactive oxygen species (ROS), being accompanied by mitochondrial depolarization, suggesting that hSMase targeted mitochondria, leading to oxidative stress. Accordingly, hepatocytes displayed a selective sensitivity to hSMase in contrast to bSMase exposure, and depletion of GSH stores enhanced susceptibility to hSMase as a result of potentiation of ROS formation and caspase 3 activation. Thus, these findings reveal the ability of ASMase to induce oxidative stress as a result of the targeting of mitochondria, and that GSH depletion sensitizes hepatocytes to the ASMase-induced apoptosis.

Animals↗
PubMed2005

Chemical and pathological oxidative influences on band 3 protein anion-exchanger.

BACKGROUND/AIMS: The erythrocyte is a cell exposed to a high level of oxygen pressure and to oxidative chemical agents. This stress involves SH-groups oxidation, cell shrinkage by activation of K-Cl co-transport (KCC) and elevation of the band 3 tyrosine phosphorylation level. The aim of our study was to test whether oxidative stress could influence band 3-mediated anion transport in human red blood cells. METHODS: To evaluate this hypothesis, normal and pathological (glucose 6 phosphate dehydrogenase (G6PDH) defficient) erythrocytes were treated with known sulphydryl-blocking or thiol-oxidizing agents, such as N-ethylmaleimide (NEM), azodicarboxylic acid bis[dimethylamide] (diamide), orthovanadate, Mg2+ and tested for sulphate (SO4-) uptake, K+ efflux, G6PDH activity and glutathione (GSH) concentration. RESULTS: In normal red blood cells, the rate constants of SO4- uptake decreased by about 28 % when cells were incubated with NEM, diamide and orthovanadate. In G6PDH-deficient red blood cells, in which oxidative stress occurs naturally, the rate constant of sulphate uptake was decreased by about 40% that of normal red cells. Addition of oxidizing and phosphatase inhibitor agents to pathological erythrocytes further decreased anion transport. In contrast, G6PDH activity was increased under oxidative stress in normal as well as in pathological cells and was lower in the presence of exogenous Mg2+ in parallel to a significant increase in sulphate transport. In both cells, the oxidizing agents increased K+ efflux with depletion of GSH. CONCLUSION: The data are discussed in light of the possible opposite effects exerted by oxidative agents and Mg2+ on KCC and on the protein tyrosine kinase (PTK)-protein tyrosine phosphatase (PTP) equilibrium. The decreased sulphate uptake observed in the experimental and pathological conditions could be due to band 3 SH-groups oxidation or to oxidative stress-induced K-Cl symport-mediated cell shrinkage with concomitant band 3 tyrosine phosphorylation.

Anion Exchange Protein 1, Erythrocyte↗
PubMed2003

Mg citrate found more bioavailable than other Mg preparations in a randomised, double-blind study.

Published data on the bioavailability of various Mg preparations is too fragmented and scanty to inform proper choice of Mg preparation for clinical studies. In this study, the relative bioavailability of three preparations of Mg (amino-acid chelate, citrate and oxide) were compared at a daily dose of 300 mg of elemental Mg in 46 healthy individuals. The study was a randomised, double-blind, placebo-controlled, parallel intervention, of 60 days duration. Urine, blood and saliva samples were taken at baseline, 24 h after the first Mg supplement was taken ('acute' supplementation) and after 60 days of daily Mg consumption ('chronic' supplementation). Results showed that supplementation of the organic forms of Mg (citrate and amino-acid chelate) showed greater absorption (P = 0.033) at 60 days than MgO, as assessed by the 24-h urinary Mg excretion. Mg citrate led to the greatest mean serum Mg concentration compared with other treatments following both acute (P = 0.026) and chronic (P = 0.006) supplementation. Furthermore, although mean erythrocyte Mg concentration showed no differences among groups, chronic Mg citrate supplementation resulted in the greatest (P = 0.027) mean salivary Mg concentration compared with all other treatments. Mg oxide supplementation resulted in no differences compared to placebo. We conclude that a daily supplementation with Mg citrate shows superior bioavailability after 60 days of treatment when compared with other treatments studied.

Biological Availability↗
PubMed1990

Effect of lime composition on the formation of reactive oxygen species from areca nut extract in vitro.

Lime, representative of that used by betel quid chewers, was collected in a region of Papua New Guinea where the incidence of oral cancer is high. The free calcium hydroxide content and pH of 25 lime samples were highly correlated with the generation of reactive oxygen species from areca nut extract in vitro, and DNA damage in vitro, measured as 8-hydroxy-2'-deoxyguanosine. Fe2+ and Mg2+ levels in the lime samples were too low to modify formation of reactive oxygen species, but hydrogen peroxide formation was almost entirely inhibited by addition of Mg2+ to the reaction mixture. These results suggest that the calcium hydroxide content of lime in the presence of areca nut is primarily responsible for the formation of reactive oxygen species which might cause oxidative damage in the DNA of buccal mucosa cells of betel quid chewers.

8-Hydroxy-2'-Deoxyguanosine↗
PubMed1997

The malaria parasite supplies glutathione to its host cell--investigation of glutathione transport and metabolism in human erythrocytes infected with Plasmodium falciparum.

Malaria-infected red blood cells are under a substantial oxidative stress. Glutathione metabolism may play an important role in antioxidant defense in these cells, as it does in other eukaryotes. In this work, we have determined the levels of reduced and oxidized glutathione (GSH and GSSG, respectively) and their distributions in the parasite, and in the host-cell compartments of human erythrocytes infected with the malaria parasite Plasmodium falciparum. In intact trophozoite-infected erythrocytes, [GSH] is low and [GSSG] is high, compared with the levels in normal erythrocytes. Normal erythrocytes and the parasite compartment display high GSH/GSSG ratios of 321.6 and 284.5, respectively, indicating adequate antioxidant defense. This ratio drops to 26.7 in the host-cell compartment, indicating a forceful oxidant challenge, the low ratios resulting from an increase in GSSG and a decline in GSH concentrations. On the other hand, the concentrations of GSH and GSSG in the parasite compartment remain physiological and comparable to their concentrations in normal red blood cells. This results from de novo glutathione synthesis and its recycling, assisted by the intensive activity of the hexose monophosphate shunt in the parasite. A large efflux of GSSG from infected cells has been observed, its rate being similar from free parasites and from intact infected cells. This result suggests that de novo synthesis by the parasite is the dominating process in infected cells. GSSG efflux from the intact infected cell is more than 60-fold higher than the rate observed in normal erythrocytes, and is mediated by permeability pathways that the parasite induces in the erythrocyte's membrane. The main route for GSSG efflux through the cytoplasmic membrane of the parasite seems to be due to a specific transport system and occurs against a concentration gradient. Gamma-glutamylcysteine [Glu(-Cys)] and GSH can penetrate through the pathways from the extracellular space into the host cytosol, but not into that of the parasite. This implies that the parasite membrane is impermeable to these peptides, and that the host cannot supply GSH to the parasite as suggested previously. Exogenous Glu(-Cys) is not converted into GSH in the host cell, arguing that GSH synthetase may not be functional. Compartment analysis of Mg2+ in infected erythrocytes revealed that the host compartment exhibits a low concentration of Mg2+ (0.5 mM) in comparison with the parasite compartment (4 mM) and the normal erythrocytes (1.5-3 mM). The drop in [Mg2+] results in cessation of Glu(-Cys) synthesis, and hence of GSH synthesis in the host-cell compartment. The decrease in [Mg2+] can affect other Mg2+-ATP-dependent functions, such as Na+ and Ca2+ active efflux. The present investigation confirms that the host-cell compartment is oxidatively distressed, whereas the parasite is efficiently equipped with anti-oxidant means that protect the parasite from the oxidative injury. The parasite has a huge capacity for de novo synthesis of GSH and for the reduction of GSSG. Part of the GSSG that is actively extruded from the parasite is reduced to GSH in the host cell whose own GSH synthesis is crippled.

Animals↗
PubMed1990

[Adhesive strengths of cast crowns with various types of cements].

In an in vitro study the adhesive strength of sand-blasted castings (gold alloy) was tested on human teeth prepared and finished in different ways. For cementation we used two glass ionomer and one phosphate cement. On the surfaces treated with carbide finishing instruments the force required for separating the crown from the tooth was about 1.9 N/mm2 for Ketac-cem, about 2 N/mm2 for Fuji Ionomer, and about 1.8 N/mm2 for Harvard (a zinc oxide phosphate cement). Compared with this, the values obtained for dentin surfaces pretreated with fine diamonds (red ring) were 1.5 N/mm2 for Ketac-cem, 1.6 N/mm2 for Fuji Ionomer, and 1.9 N/mm2 for Harvard. The measured differences between the various types of cement were statistically not significant.

Crowns↗
PubMed2004

Thermal expansion typed investments for casting titanium.

New investments for titanium were developed by adding ZrC and ZrN as additives for thermal expansion to an MgO cement base investment with setting shrinkage and low thermal expansion. Setting, thermal and residual expansion, X-ray diffraction and compressive strength of these experimental investments, surface roughness of the cast plate and casting accuracy of titanium crowns were evaluated. Thermal expansion of investments increased with additive amounts, and residual expansion occurred even when cooling to room temperature after firing in an air atmosphere by the oxidation to ZrO2 of these additives. The casting accuracy of full-crowns cast into molds at room temperature correlated with the content of ZrC and ZrN. As the result the cast titanium crown could be obtained with low surface roughness and good adaptability.

Analysis of Variance↗
PubMed1997

The activation by magnesium treatment of anti-oxidants eliminating the oxygen free radicals in Drosophila melanogaster in vivo.

Drosophila melanogaster adults of the Oregon R and Canton S wild-type stocks were fed for 24 h with 0.10 M, 0.25 M and 0.50 M MgCl2 in 1 per cent sugar solution. This treatment resulted in a significant increase (10-50 per cent) in the activities of the enzymes superoxide dismutase (SOD) and catalase as well as in the concentration of the non-enzymatic antioxidant glutathione (GSH). The increased activities could be due to the increased synthesis caused by the Mg treatment.

Animals↗
PubMed2003

Quantitative evaluation of antibacterial activities of metallic oxide powders (ZnO, MgO and CaO) by conductimetric assay.

Antibacterial activities of metallic oxide (ZnO, MgO and CaO) powders against Staphylococcus aureus and Escherichia coli were quantitatively evaluated by measuring the change in electrical conductivity of the growth medium caused by bacterial metabolism (conductimetric assay). The obtained conductivity curves were analyzed using the growth inhibition kinetic model proposed by Takahashi for calorimetric evaluation, and the metallic oxides were determined for the antibacterial efficacy and kinetic parameters. The parameters provide some useful indicators for antimicrobial agents, such as the dependence of antibacterial activity on agent concentration, and the affinity between the agent and the bacterial cells. CaO was the most effective, followed by MgO and ZnO, against E. coli. On the other hand, ZnO was the most effective for S. aureus and was suggested to have a strong affinity to the cells of S. aureus.

Anti-Bacterial Agents↗