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At least 145 records · Page 8Linked to original sources
PubMed1995

A re-evaluation of the ultrastructural localization of 5'-nucleotidase activity in the developing rat cerebellum, with a cerium-based method.

The membrane ectoenzyme 5'-nucleotidase converts 5'-AMP into adenosine which, in the nervous tissue, plays an important role as intercellular messenger. Moreover, during histogenesis, 5'-nucleotidase seems to be related to cell proliferation and migration. Conflicting data are reported in the literature about the localization (neuronal or glial) of 5'-nucleotides in the rat cerebellum. In the present report we have analyzed the distribution of 5'-nucleotidase activity with electron microscopy, using a cerium-based method, at different postnatal histogenetic stages (postnatal days (PND) 11, 17, 28). On PND 11 and 17, rims of reaction product outlined the plasma membranes of some neuroblasts in the external granular layer and of parallel fibers and some migrating cells in the developing molecular layer. Positivity was frequently observed on membranes of adjacent neuronal cells and glial processes. Moderate activity was also present on the membranes of granule cells and of mossy fiber rosettes and granule cell dendrites constituting the cerebellar glomeruli within the internal granule cell layer. At PND 28, the reaction product was slightly reduced in some localizations. Cytochemical patterns prove that the cerium-based method is suitable for demonstration of 5'-nucleotidase-specific activity. In fact, a continuous and fine reaction product appears strictly linked to the cell membranes, and no unevenly scattered precipitates can be observed. Data suggest that, during cerebellar histogenesis, 5'-nucleotidase may be involved in the mechanisms of cell migration and proliferation. However, in adulthood, prominent localization of the reaction product on neuronal elements suggests a major role in neuromodulation processes for the enzyme.

5'-Nucleotidase↗
PubMed1982

In vitro inactivation of silver sulphadiazine by the addition of cerium salts.

Silver sulphadiazine, with and without cerium salts, was tested in an in vitro topical antimicrobial susceptibility test assay for antimicrobial activity against microorganisms isolated from burn wounds. Compared to silver sulphadiazine alone the addition of cerium to silver sulphadiazine generally reduced the diameter of the antimicrobial inhibitory zones around susceptible organisms. In addition, complete nullification of the activity of silver sulphadiazine occurred in many instances.

Bacteria↗
PubMed1992

Survival in major burn injuries treated by one bathing in cerium nitrate.

Sixty-four patients aged 16-74 years with total body surface area burns (TBSA) ranging from 30 to 90 per cent, were given one bathing in 0.04 M cerium nitrate within 4 h of admission to hospital. Of 21 patients aged 16-30 years, one died (aged 28 with 90 per cent TBSA), and of those aged 31-74 years, two died, one (aged 50 years with 55 per cent TBSA) had multiple internal injuries, the other (aged 51 years with 55 per cent TBSA) had a pulmonary embolism at day 19. Two risk scores, developed from data on 11,200 burn patients treated by standard methods (Roi et al. 1983), were applied to the analysis of risk for 59 patients for whom both total burn surface (TB) and full thickness (FT) areas had been recorded. About 20 patients bore risk of 0.8 or greater on the FT scale and 1.0 on the TB scale, yet instead of 80 per cent deaths among these, only two died. No FT assessment had been made on the multiple injury death whose TB risk score was 0.66. Such survival results in high-risk patients should encourage the use of cerium nitrate for treating serious burn injury.

Adolescent↗
PubMed2005

Antineoplastic activity of new lanthanide (cerium, lanthanum and neodymium) complex compounds.

Cerium (III), lanthanum (III) and neodymium (III) complexes with 3,3'-benzylidenebis[4-hydroxycoumarin] were synthesized in view of their application as cytotoxic agents. The complexes were characterized by different physicochemical methods: elemental analysis, mass spectrometry, 1H NMR, 13C NMR and IR spectroscopy. The spectra of the complexes were interpreted on the basis of comparison with the spectrum of the free ligand. The vibrational analysis showed that in the complexes the ligand coordinated to the metal ion through both deprotonated hydroxyl groups; however, participation of the carbonyl groups in the coordination to the metal ion was also suggested. The evaluation of the cytotoxic activity of the novel lanthanide complexes on HL-60 myeloid cells revealed that they are potent cytotoxic agents. The cerium complex was found to exhibit superior activity in comparison to the lanthanum and neodymium coordination compounds, the latter being the least active. Our data give us reason to conclude that the newly synthesized lanthanide complexes should be submitted to further more detailed pharmacological and toxicological evaluation.

4-Hydroxycoumarins↗
PubMed2005

Orally administrated rare earth element cerium induces metallothionein synthesis and increases glutathione in the mouse liver.

The influence of oral administration of rare earth element cerium (Ce) was studied in relation to metallothionein (MT) and glutathione (GSH) content in the organs of ICR mice, which were administered heavy metal cadmium (Cd) for comparison. Male ICR mice were divided into 9 groups: 1 control group, 4 cerium groups and 4 cadmium groups, each with 4 mice, for a total of 36 mice. Ce groups included a 20 ppm CeCl3 diet (Ce-low) group and a 200 ppm CeCl3 diet (Ce-high) group, as did Cd groups, i.e., a 20 ppm CdCl2 diet (Cd-low) group and a 200 ppm CdCl2 diet (Cd-high) group. Each group was subdivided in 2 groups except a control group: 6-week administration group and 12-week administration group. The level of plasma aspartate aminotransferase(AST) activity, plasma alanine aminotransferase(ALT) activity, plasma cholesterol and plasma triglyceride in the Ce-low, Cd-low, Ce-high, and Cd-high group were higher than that of control group, although there were no significant differences (p > 0.05). By contrast, both Ce and Cd groups had higher levels of MT and GSH in hepatic cells compared to the control group (p < 0.05) and decreased liver tissue level of lipoperoxide (p < 0.05). These groups also had decreased plasma superoxide dismutase (SOD) activity (p < 0.05), and increased plasma level of lipoperoxide (p > 0.05). In conclusion, it is suggested that orally administered Ce increases MT and GSH as an antioxidant in the mouse liver, and these reaction are probably caused by increases in the oxidative stress with Ce.

Administration, Oral↗
PubMed1987

Cytotoxicity of the rare earth metals cerium, lanthanum, and neodymium in vitro: comparisons with cadmium in a pulmonary macrophage primary culture system.

The rare earth metals cerium, lanthanum, and neodymium each were evaluated in an in vitro cytotoxicity assay system using adult, male Sprague-Dawley rat pulmonary alveolar macrophages. Both the soluble chloride form of these metals and their insoluble metal oxides were studied. For comparison purposes, the cytotoxicities of cadmium chloride and cadmium oxide were also quantified in this test system. In general, regardless of the cytotoxicity parameter measured, i.e., cell viability, lysosomal enzyme leakage, or changes in cell surface morphology, cadmium was more toxic to these cells than were the rare earth metals. Of the rare earth metals studied, only lanthanum chloride (LC50 = 52 microM), cerium chloride (LC50 = 29 microM), and neodymium oxide (LC50 = 101 microM) displayed significant cytotoxicity in this test system. Cadmium chloride exhibited an LC50 value of 28 microM, whereas the LC50 value for cadmium oxide was found to be 15 microM. These findings suggest that rare earth metal fumes should be considered as cytotoxic to lung tissue and therefore potentially fibrogenic.

Animals↗
PubMed2002

Rapid ion chromatography of L-ascorbic acid, nitrite, sulfite, oxalate, iodide and thiosulfate by isocratic elution utilizing a postcolumn reaction with cerium(IV) and fluorescence detection.

Rapid separation and determination of mixtures of L-ascorbic acid, nitrite, sulfite, oxalate, iodide and thiosulfate by conventional ion chromatography is often difficult due to incomplete separation of L-ascorbic acid and nitrite from the water peak when using eluents giving short elution times for iodide and thiosulfate. Separation of the six species within about 15 min has been achieved by isocratic elution using a resin-based ion-exchange column with a carbonate eluent containing a trace amount of 1,3,5-benzenetricarboxylic acid (BTA) and fluorescence measurement of cerium(III) formed via postcolumn reactions of the separated sample species with cerium(IV). Calibration plots of peak height versus concentration were linear up to 10.0 microM (1.76 ppm) for L-ascorbic acid, 8.0 microM (0.37 ppm) for nitrite, 8.0 microM (0.70 ppm) for oxalate, 80.0 microM (10.2 ppm) for iodide and 25.0 microM (2.80 ppm) for thiosulfate, whilst the sulfite calibration was linear up to 25.0 microM (2.00 ppm) when peak area was plotted against concentration. Detection limits (defined as S/N = 3) were 18 ppb for L-ascorbic acid, 4 ppb for nitrite, 16 ppb for sulfite, 7 ppb for oxalate, 72 ppb for iodide and 37 ppb for thiosulfate. The proposed method was applied successfully to the determination of L-ascorbic acid, nitrite, sulfite, oxalate, iodide or thiosulfate in water samples.

Anions↗
PubMed1991

Light microscopical detection of H2O2-generating oxidases using cerium ions and aqueous incubation media.

Light microscopical procedures were optimized and tested for specificity for the histochemical demonstration of D-amino acid oxidase, alpha-hydroxy acid oxidase, monoamine oxidase, and xanthine oxidase using cerium ions and a visualization step originally described by Angermüller and Fahimi (1988a, b), and modified for D-amino acid oxidase by Gossrau et al. (1989). The visualization medium contained diaminobenzidine, cobalt ions, and small amounts of hydrogen peroxide. Procedures of pretreatment of cryostat sections, types of substrate, concentrations of substrates, and cerium ions were varied. Optimum procedures are reported for the detection of these oxidases in different rat tissues. The results are compared with those obtained with other methods described for the demonstration of hydrogen peroxide-generating oxidases such as the tetrazolium, Hatchett Brown, and coupled peroxidatic methods.

Alcohol Oxidoreductases↗
PubMed1978

Investigation of cerium and yttrium ions effects on microbial nitrogen fixation and determination of inhibition.

Critical investigation of the effect of yttrium and cerium ions in culture media for nitrogen-fixing bacteria showed strong inhibition. There was a decrease in the amount of nitrogen fixed; simultaneously, in the samples containing cerium ions, carbon consumption values increased as the molarity of metal ion was enhanced. Inhibition rate was invariably maximum at the highest concentration of metal ions.

Bacteria↗
PubMed2004

Recent advances in synthetic transformations mediated by cerium(IV) ammonium nitrate.

Cerium(IV) ammonium nitrate (CAN) has recently emerged as a versatile reagent for oxidative electron transfer; the overwhelming number of reports serve as a testimony to the unparalleled utility of CAN in a variety of transformations of synthetic importance. Our recent work has uncovered novel carbon-carbon bond-forming reactions leading to the one-pot synthesis of dihydrofurans, tetrahydrofurans, and aminotetralins. In addition, we have developed a number of facile carbon-heteroatom bond-forming reactions by the CAN-mediated oxidative addition of soft anions to alkenes. A mechanistic rationale has been provided for the reactions explored. As might be expected of very powerful one-electron oxidants, the chemistry of cerium(IV) oxidation of organic molecules is dominated by radical and radical cation chemistry.

Cerium↗
PubMed2005

Effect of water/fuel emulsions and a cerium-based combustion improver additive on HD and LD diesel exhaust emissions.

One of the major technological challenges for the transport sector is to cut emissions of particulate matter (PM) and nitrogen oxides (NOx) simultaneously from diesel vehicles to meet future emission standards and to reduce their contribution to the pollution of ambient air. Installation of particle filters in all existing diesel vehicles (for new vehicles, the feasibility is proven) is an efficient but expensive and complicated solution; thus other short-term alternatives have been proposed. It is well known that water/diesel (W/ D) emulsions with up to 20% water can reduce PM and NOx emissions in heavy-duty (HD) engines. The amount of water that can be used in emulsions for the technically more susceptible light-duty (LD) vehicles is much lower, due to risks of impairing engine performance and durability. The present study investigates the potential emission reductions of an experimental 6% W/D emulsion with EURO-3 LD diesel vehicles in comparison to a commercial 12% W/D emulsion with a EURO-3 HD engine and to a Cerium-based combustion improver additive. For PM, the emulsions reduced the emissions with -32% for LD vehicles (mass/km) and -59% for the HD engine (mass/ kWh). However, NOx emissions remained unchanged, and emissions of other pollutants were actually increased forthe LD vehicles with +26% for hydrocarbons (HC), +18% for CO, and +25% for PM-associated benzo[a]pyrene toxicity equivalents (TEQ). In contrast, CO (-32%), TEQ (-14%), and NOx (-6%) were reduced by the emulsion for the HD engine, and only hydrocarbons were slightly increased (+16%). Whereas the Cerium-based additive was inefficient in the HD engine for all emissions except for TEQ (-39%), it markedly reduced all emissions for the LD vehicles (PM -13%, CO -18%, HC -26%, TEQ -25%) except for NOx, which remained unchanged. The presented data indicate a strong potential for reductions in PM emissions from current diesel engines by optimizing the fuel composition.

Air Pollution↗
PubMed2005

Kinetics of phosphodiester cleavage by differently generated cerium(IV) hydroxo species in neutral solutions.

Neutral aqueous solutions of cerium ammonium nitrate obtained by dilution of their acetonitrile stock solution with imidazole buffer show high catalytic activity in the hydrolysis of bis(p-nitrophenyl) phosphate (BNPP) and better reproducibility than other similar systems, but suffer from low stability. The kinetics of catalytic hydrolysis is second-order in Ce(IV), independent of pH in the range 5-8 and tentatively involves the Ce2(OH)7+ species as the active form. Attempts to stabilize the active species by different types of added ligands failed, but the use of Ce(IV) complexes pre-synthesized in an organic solvent with potentially stabilizing ligands as precursors of active hydroxo species appeared to be more successful. Three new Ce(IV) complexes, [Ce(Phen)2O(NO3)2], [Ce(tris)O(NO3)(OH)] and [Ce(BTP)2(NO3)4].2H2O (BTP = bis-tris propane, 1,3-bis[tris(hydroxymethyl)methylamino]propane), were prepared by reacting cerium ammonium nitrate with the respective ligands in acetonitrile and were characterized by analytical and spectroscopic techniques. Aqueous solutions of these complexes undergo rapid hydrolysis producing nearly neutral polynuclear Ce(IV) oxo/hydroxo species with high catalytic activity in BNPP hydrolysis. Potentiometric titrations of the solutions obtained from the complex with BTP revealed the formation of Ce4(OH)15+ species at pH > 7, which are protonated affording Ce4(OH)14(2+) and then Ce4(OH)13(3+) on a decrease in pH from 7 to 5. The catalytic activity increases strongly on going to species with a higher positive charge. The reaction mechanism involves first- and second-order in catalyst paths as well as intermediate complex formation with the substrate for higher charged species.

Cerium↗
PubMed2004

Selective catalytic oxidation of ammonia over copper-cerium composite catalyst.

This work considers the oxidation of ammonia (NH3) by selective catalytic oxidation (SCO) over a copper (Cu)-cerium (Ce) composite catalyst at temperatures between 150 and 400 degrees C. A Cu-Ce composite catalyst was prepared by coprecipitation of copper nitrate and cerium nitrate at various molar concentrations. This study also considers how the concentration of influent NH3 (500-1000 ppm), the space velocity (72,000-110,000 hr(-1)), the relative humidity (12-18%) and the concentration of oxygen (4-20%) affect the operational stability and the capacity for removing NH3. The effects of the O2 and NH3 content of the carrier gas on the catalyst's reaction rate also are considered. The experimental results show that the extent of conversion of NH3 by SCO in the presence of the Cu-Ce composite catalyst was a function of the molar ratio. The NH3 was removed by oxidation in the absence of Cu-Ce composite catalyst, and approximately 99.2% NH3 reduction was achieved during catalytic oxidation over the Cu-Ce (6:4, molar/molar) catalyst at 400 degrees C with an O2 content of 4%. Moreover, the effect of the initial concentration and reaction temperature on the removal of NH3 in the gaseous phase was also monitored at a gas hourly space velocity of less than 92,000 hr(-1).

Ammonia↗
PubMed2004

XANES quantitative structural determination of the sandwich bis(naphthalocyaninato) cerium complex.

The molecular structure of the sandwich double-decker bis(naphthalocyaninato) cerium complex was determined for the first time in a quantitative way using a new method of analysis of the Ce L3-edge X-ray absorption near-edge structure (XANES) in the framework of the full multiple scattering theory. An average Ce-N bond length of 2.47 A was determined. In this complex structure the pyrrole rings play the key role in the determination of the XANES spectral features, and the differences in bond lengths between the Ce atom and the eight pyrrole N atoms are 0.14 A, addressing a significant distortion of these rings around cerium. These results may be used to study double-decker imidazole rings, present as the structure model in the photosynthesis center and in sandwich-structured lanthanide chlorophyll molecules.

Cerium↗
PubMed1962

Cerium-144 in food.

Small amounts of cerium-144 have been found in samples of food and animal bone obtained from Ibaraki, Japan. The highest level of radioactivity was detected in clams (Schizimi, Corbicura sp.) harvested from Hinuma Marsh. In view of the widespread occurrence of cerium-144 in tested samples, it is assumed that the presence of this radionuclide is due to fallout.

Animals↗
PubMed1985

Changing patterns of cerium reactivity in developing ovarian oocytes of the hamster.

In developing ovarian oocytes of 2-day-old, 12-day-old and adult hamsters, oxidative enzyme activity as demonstrated by the cerium technique is strongest at 12 days and occurs principally in those oocytes which have begun rapid growth. The reaction is associated with the outer mitochondrial membrane, nearby cytoplasm, endoplasmic reticulum and nuclear envelope. Once antrum formation has begun and the mitochondria have reached the dormant (storage) stage, cerium reactivity ceases. In adults, reaction occurs at the same stages of oocyte development but is weaker and limited to the mitochondria and their immediate vicinity.

Age Factors↗
PubMed1975

Prevention of radiation pneumonitis from inhaled cerium-144 by lung lavage in beagle dogs.

This study was performed to evaluate bronchopulmonary lavage and chelation therapy as a treatment method to prevent the development of radiation pneumonitis after inhalation of a radioactive aerosol. Twelve beagle dogs were exposed to an aerosol of cerium-144 in fused clay particles resulting in initial lung burdens from 47 to 64 muCi of 144-Ce per kg of body weight. Eight of the dogs were treated with a series of 10 bronchopulmonary lavages and 10 intravenous injections of calcium diethylenetriamine pentaacetate acid during the first 56 days after exposure to remove the deposited 144-Ce; the remaing 4 exposed dogs receiged no treatment. An additional 4 dogs were exposed to stable cerium and were given the course of treatment as an additional control group. Three of the 4 untreated dogs and 2 of the 8 treated dogs died 171 to 246 days after exposure with radiation pneumonitis or pulmonary fibrosis, or both. All but one of the remaining dogs were alive and apparently in good clincial health 550 dyas after exposure; the one dog had radiographic indications of pulmonary fibrosis by 365 days after exposure. The relative distribution of 144-Ce in the lungs and other major organs was similar in the treated and untreated dogs that died.

Aerosols↗
PubMed2006

Room temperature formation of ammonia by oxidizing hydrogenated cerium nanoparticles in the air.

Ammonia formation was observed when hydrogenated cerium nanoparticles prepared by hydrogen plasma-metal reaction (HPMR) were exposed to the air at room temperature. This novel phenomenon represents a successful example of room temperature cleavage of dinitrogen and may find application in low temperature synthesis of ammonia under thermodynamically favorable conditions. A possible mechanism is also proposed. We suggest that the oxidation of cerium hydride offers chemical force to drive the hydrogen atoms out of the lattice. The monoatomic H released to the surface is highly active and readily reacts with N2 to yield ammonia. Some surface processes, which we know little about at the moment, are likely to be involved so as to lower the energy barrier of nitrogen dissociation. Further investigation is required to elucidate the detailed mechanism.

Air↗