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  • 1
    ISSN: 1432-2277
    Keywords: Key words Liver transplantation ; venovenous bypass ; heparin coating ; Venovenous bypass ; heparin coating ; liver transplantation ; Heparin coating ; venovenous bypass ; liver transplantation ; Leukocyte activation ; cytokines ; liver transplantation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We used an in vitro model for venovenous bypass in a prospective, randomized study to analyze the effect on leukocytes cell activation after coating the total blood contact surface with covalently bound heparin. In ten experiments heparin-coated circuits were used, and in ten other experiments noncoated circuits were used. Monocyte cytokine production and neutrophil myeloperoxidase release were analyzed. Monocytes were isolated using anti-CD14 paramagnetic beads, and oligo(dT)25 beads were used to isolate mRNA before subsequent reverse transcription and semiquantitative amplification of various cytokines in order to determine time-related changes in expression during bypass. After 2 h, mRNAs for IL-1β and IL-6 were highly upregulated in noncoated compared to heparin-coated circuits. Little or no change was seen in the expression of other cytokines. IL-1β and IL-6 were measured in plasma after 12 h and reflected the upregulated mRNAs in noncoated circuits. A significantly reduced release of myeloperoxidase was observed in coated versus noncoated circuits. This indicates that heparin-coated surfaces reduce cellular activation and the release of inflammatory mediators.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 127 (1996), S. 173-176 
    ISSN: 1434-4475
    Keywords: Reissert compound ; Intramolecular cyclization ; 2-Benzyloxy-3-methoxy-8H-dibenzo-[a,g]-8-quinolizione ; (±)-Bharatamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Alkylation of theReissert compound1 by methyl 2-bromomethylbenzoate (2) followed by spontaneous intramolecular cyclization affords dibenzo [a,g]quinolizinone4 which in turn can be reduced to benzyl ether5 by LiAlH4/NaBH4. Debenzylation of5 by ethanolic HCl furnishes the title compound6 in improved total yield.
    Type of Medium: Electronic Resource
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