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  • 11
    ISSN: 1420-9071
    Keywords: Xestobergsterol A ; histamine release ; PI-PLC ; IP3 ; signal transduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Histamine release from rat peritoneal mast cells induced by anti-IgE was essentially complete within 4–5 min. Xestobergsterol A and B, which are constituents of the Okinawan marine spongeXestospongia bergquistia Fromont, dose-dependently inhibited anti-IgE-induced histamine release from rat mast cells. The IC50 values of xestobergsterol A and B for histamine release in mast cells activated by anti-IgE were 0.07 and 0.11 μM, respectively. Anti-IgE stimulated PI-PLC activity in a mast cell membrane preparation. Xestobergsterol A dose-dependently inhibited the generation of IP3 and membrane-bound PI-PLC activity. Moreover, xestobergsterol A inhibited Ca2+-mobilization from intracellular Ca2+-stores as well as histamine release in mast cells activated by anti-IgE. On the other hand, xestobergsterol B did not inhibit the membrane-bound and cytosolic PI-PLC activity, IP3 generation or the initial rise in [Ca2+]i in mast cells activated by anti-IgE. These results suggest that the mechanism of inhibition by xestobergsterol A of the initial rise in [Ca2+]i, of the generation of IP3, and of histamine release induced by anti-IgE, was through the inhibition of PI-PLC activity.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 5149-5153 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polymethyl methacrylate (PMMA) film bonded by 4-META dental adhesive resin to mild steel was used as a specimen to study the mechanism of water permeation into the adhesive interface. Degradation of the adhesion interface after immersion in water was investigated by measurement of peeling area after imposing thermal stress using liquid nitrogen. The amount of water penetrated at the interface was calculated from the solution to Fick's second equation. The degradation at the interface is discussed with respect to the water content. Water enters the interface by diffusion through the resin rather than by passage along the interface. The interface is broken by water when the water content at the interface reaches 48% of the equilibrium water concentration of PMMA. Observation through the PMMA film shows no change in the mild steel surface at 48% equilibrium water concentration; at 95% water content many small white spots appear on the surface. The surface colour gradually changes to black due to the formation of corrosion products.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 27 (1992), S. 5149-5153 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polymethyl methacrylate (PMMA) film bonded by 4-META dental adhesive resin to mild steel was used as a specimen to study the mechanism of water permeation into the adhesive interface. Degradation of the adhesion interface after immersion in water was investigated by measurement of peeling area after imposing thermal stress using liquid nitrogen. The amount of water penetrated at the interface was calculated from the solution to Fick's second equation. The degradation at the interface is discussed with respect to the water content. Water enters the interface by diffusion through the resin rather than by passage along the interface. The interface is broken by water when the water content at the interface reaches 48% of the equilibrium water concentration of PMMA. Observation through the PMMA film shows no change in the mild steel surface at 48% equilibrium water concentration; at 95% water content many small white spots appear on the surface. The surface colour gradually changes to black due to the formation of corrosion products.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 28 (1993), S. 3764-3768 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The mechanism destroying the adhesion between PMMA and mild steel, and the action of water molecules reaching the adhesion interface was investigated. Mild steel and a thin PMMA film were bonded with dental adhesive (4-META resin). After immersion in water, the adhesive layer was peeled from the metal surface. The surface was analysed by ESCA, reflection electron diffraction, and X-ray diffraction to elucidate changes in surface structure. After 2 weeks immersion, there was a very thin brown product and after 2 months a thick black corrosion product composed of Fe3O4 formed at the adhesion interface. The thin brown layer showed no X-ray diffraction pattern but reflection electron diffraction showed it to be FeO(OH). After 3 days immersion, the mild steel surface appeared unchanged through the clear resin layer, and ESCA analysis showed the same chemical state as the surface of the specimen immersed for 2 weeks. Destruction of adhesion between metal and adhesive is caused by destruction of the chemical bond by the water molecules permeating through the resin layer. It is followed by corrosion of mild steel which produced iron oxide hydrate.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Two kinds of time differential Mössbauer spectra of57Co-labelled Co(BrO3)2·6H2O were measured at room temperature by delayed coincidence technique, i.e., one was the delayed coincidence between 122 keV γ ray and 14.4 keV γ ray (γ, γ-ray coincidence), and another was the coincidence between 6.3 keV KX ray and 14.4 keV γ ray (X, γ-ray coincidence). The time dependence of chemical states of57Fe-species were observed on γ, γ-ray and X, γ-ray coincidence Mössbauer spectra. The relative area intensities of57Fe(II) observed on the X, γ-ray coincidence spectra were larger than those on the γ, γ-ray coincidence spectra on every time windows.
    Type of Medium: Electronic Resource
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  • 16
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Mixed-valence states of57Fe-atoms produced after EC-decay of57Co in oxo-centered trinuclear cobalt-iron carboxylates have been studied by means of emission Mössbauer spectroscopy. The emission Mössbauer spectra show nearly the same temperature dependence of the mixed-valence state as found in the absorption Mössbauer spectra of the corresponding trinuclear iron carboxylates. The results indicate that most of the decayed atoms keep their position at the sites of original57Co atoms.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 154 (1991), S. 95-102 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Coincidence Mössbauer spectra of57Co-labelled [CoFe2O(CH3CO2)6(H2O)3] were determined at 78 K and 298 K with three timewindows of 0–50, 50–150 and 150–300 ns. Temperature dependence in the spectral shape ascribed to an intramolecular electron transfer was observed in all the time-window spectra, while little time dependence was observed. The results indicate that57Fe atoms produced by EC-decay are incorporated in a chemical environment similar to that of the parent57Co atoms, forming a trinuclear FeIIFe2 III structure at an early stage after the EC-decay.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Mixed-valence states of57Fe atoms produced after EC-decay of57Co in a series of trinuclear cobalt-iron halogenoacetate complexes, [CoIIFe 2 III O(CH3−nXnCO2)6(H2O)3] (0≤n≤3, X=Cl, Br, and I), were studied by comparing the results obtained by emission Mössbauer spectroscopy with those observed in absorption Mössbauer spectra of analogous trinuclear iron complexes, [FeIIFe 2 III O(CH3−nXnCO2)6(H2O)3]. Some of the emission Mössbauer spectra show a temperature-dependent mixed-valence state as found in the absorption Mössbauer spectra. Others show a somewhat different temperature dependence compared with the absorption Mössbauer spectra. The results were interpreted in terms of after-effects of the EC-decay.
    Type of Medium: Electronic Resource
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  • 19
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Mixed-valence states of [Fe3O(CH2ClCO2)6(H2O)3]nH2O (n=0 and 3) were studied by means of Mössbauer spectroscopy and single-crystal X-ray crystallography. The number of water molecules of crystallization was determined by X-ray crystallography. The dehydrated complex was obtained by storing the trihydrated complex under a dry atmosphere. It was found that the temperature dependence of the mixed-valence state is affected by the hydrated water molecules.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Hyperfine interactions 68 (1992), S. 197-200 
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A systematic study of organoantimony(III) compounds, SbR3, was attempted in view of the effect on Mössbauer parameters of the substituent on the aromatic ring. The Mössbauer parameters obtained in frozen organic solutions reflected the electronic effect caused by the characteristics of the substituents, electron donative or attractive, at the para position on the aromatic ring.
    Type of Medium: Electronic Resource
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