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  • 1
    ISSN: 1420-908X
    Keywords: Cartilage ; Arthritis ; Nitric oxide ; Interleukin-1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To determine the role of nitric oxide (NO) in the inhibition of aggrecan synthesis, we measured levels of NO produced by bovine chondrocytes from different layers of articular cartilage in the presence of interleukin-1 (IL-1). Chondrocytes from the superficial layer showed a large increase in NO synthesis in response to IL-1. Although chondrocytes from the deep layer also produced NO in response to IL-1, the amount was less than that from the superficial layer. Enhanced NO production evoked by IL-1 was accompanied by a significant inhibition of aggrecan synthesis. These data suggest that chondrocytes in both superficial and deep layer of articular cartilage inhibit aggrecan synthesis with IL-1 via NO production. In addition, superficial layer cells respond to lower amounts of IL-1 with respect to NO-production and inhibition of proteoglycan synthesis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-879X
    Keywords: methanol synthesis ; copper catalyst ; role of ZnO ; XPS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Methanol synthesis by the hydrogenation of CO2 over Zn-deposited polycrystalline Cu was studied using surface science techniques. The Zn sub-monolayer was oxidized by the reaction mixture during the reaction at 523 K, leading to the formation of ZnO species. The kinetic results definitely showed that the ZnO species on the Cu surface promoted the catalytic activity of methanol formation, where the activity of Cu increased by a factor of 6 at the Zn coverage of 0.17. A volcano-shaped curve was obtained for the correlation between the Zn coverage and the catalytic activity, which was very similar to the correlation curve between the oxygen coverage and the specific activity for methanol formation previously obtained for the Cu powder catalysts. The role of ZnO in Cu/ZnO based catalysts was ascribed to the stabilization of Cu+ species by the ZnO moieties on the Cu surface.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-879X
    Keywords: methanol synthesis ; copper catalyst ; oxygen coverage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The coverage of oxygen formed on the surface of catalysts during methanol synthesis from CO2 has been measured for copper-based catalysts including various metal oxides using a method called reactive frontal chromatography (RFC). An excellent correlation between the specific activity for methanol synthesis and the oxygen coverage (θ) was obtained, where the activity increased linearly with oxygen coverage atθ〈0.16 and then decreased atθ〉0.18. The results strongly indicate that the support effect or addition of metal oxides revealed in methanol synthesis over copper catalysts is ascribed to the ratio of Cu+ to Cu0 on the surface of copper particles.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-879X
    Keywords: methanol synthesis ; Cu/ZnO catalyst ; Cu-Zn alloy ; effect of reduction temperature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The behavior and role of ZnO in Cu/ZnO catalysts for the hydrogenations of CO and CO2 were studied using XRD, TEM coupled with EDX, TPD and FT-IR. As the reduction temperature increased, the specific activity for the hydrogenation of CO2 increased, whereas the activity for the hydrogenation of CO decreased. The EDX and XRD results definitely showed that ZnO x (x = 0–1) moieties migrate onto the Cu surface and dissolve into the Cu particle forming a Cu-Zn alloy when the Cu/ZnO catalysts were reduced at high temperatures above 600 K. The content of Zn dissolved in the Cu particles increased with reduction temperature and reached ∼ 18% at a reduction temperature of 723 K. The CO-TPD and FT-IR results suggested the presence of Cu+ sites formed in the vicinity of ZnO x on the Cu surface, where the Cu+ species were regarded as an active catalytic component for methanol synthesis.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 28 (2000), S. 141-146 
    ISSN: 1434-0879
    Keywords: Key words Kidney ; Nitric oxide ; Ischemia-reperfusion injury ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In this study we attempted to clarify the release of nitric oxide (NO) and its role in the ischemia-reperfusion rat kidney. After right nephrectomy, male Wistar rats were divided into four groups: one sham operated and three groups who underwent ischemia (30 min) and reperfusion of the left renal artery. Thirty minutes prior to ischemia-reperfusion, two groups were injected intraperitoneally with 10 and 30 mg/kg of NG-nitro-l-arginine methylester (L-NAME). Real-time monitoring of blood flow and NO release in the rat kidney was measured with a laser Doppler flowmeter and an NO-selective electrode, respectively. Serum creatinine and blood urea nitrogen (BUN) levels were measured 1 and 7 days after the induction of ischemia-reperfusion. Clamping of the renal artery decreased blood flow to 1–5% of the basal level measured before clamping. After removal of the clip, the blood flow of the 30 mg/kg L-NAME rats was significantly lower than that of the controls. Immediately following the clipping of the renal artery, NO release rapidly increased. After removing the clip, NO release immediately returned to three-quarters of the basal level. Serum creatinine and BUN levels of the ischemia-reperfusion rats were slightly but not significantly higher and those of 30 mg L-NAME rats were significantly higher than those of the control or ischemia-reperfusion rats 1 day and 7 days after ischemia-reperfusion. Our data suggest that NO acts as a cytoprotective agent in ischemia-reperfusion injury of the rat kidney.
    Type of Medium: Electronic Resource
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