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  • 1
    ISSN: 1432-2323
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Chez des souris, une brûlure cutanée a été réalisée dans des conditions contrôlées et avec un modèle standard de brûlure à haute température. Après homogénéisation à grande vitesse de la peau brûlée, une fraction toxique a été isolée par différentes techniques de purification. Nous avons démontré qu'une brûlure à température élevée produit des condensations chimiques et des aggrégats macromoléculaires dans la fraction protéinique de la peau. Les protéines plasmatiques jouent un rôle dans ces réactions. Après purification, les aggrégats macromoléculaires sont récoltés, non pas sous forme de protéines pures, mais sous forme de micelles lipo-protéiniques. Dans la fraction lipidique, on trouve des produits de décomposition thermique. Les effets biologiques de la fraction lipoprotéinique purifiée ont été étudiés sur une perfusion de foie de rat, 5 jours après injection intrapéritonéale du produit; plusieurs activités de biosynthèse du foie isolé ont été étudiées. Nous avons observé une nette réduction de la synthèse de l'urée et une dépression de la glyconéogenèse. Ces résultats biochimiques concordent avec des modifications de l'ultrastructure cellulaire: le complexe lipo-protéinique de la peau brûlée produit une vacuolisation des mitochondries des cellules hépatiques.
    Notes: Abstract Murine skin was thermally injured under controlled conditions in a standard high temperature burn model. After high-speed homogenization of the burned skin, a toxic fraction was isolated applying different purification procedures. It was demonstrated that high temperature burns produced chemical condensations and high molecular aggregates in the protein moiety of the skin. Plasma proteins were involved in these reactions. After the purification process, the high molecular aggregates were obtained not as pure proteins, but as lipid-protein micelles. In the lipid moiety itself, thermal decomposition products were detectable. The biological effects of the purified lipid-protein fraction were studied by aid of rat liver perfusions 5 days after intraperitoneal injection of the material measuring different biosynthetic activities of the isolated organ. Significantly reduced biosynthesis of urea and depressed gluconeogenesis were demonstrable. The biochemical results are paralleled by ultrastructural findings indicating that the lipid-protein complex from burned skin causes mitochondrial vacuolization in liver cells of treated animals.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1440
    Keywords: Ascites ; Liver cirrhosis ; Plasminogen ; Antiproteases ; Fibrinolysis ; Dexamethasone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fibrinolysis induced by the infusion of plasminogen activators into the circulation has been shown to cause coagulation disorders in ascites retransfusion. Dexamethasone is known to inhibit the synthesis of plasminogen activators by peritoneal macrophages. We therefore assessed its potential in preventing the occurrence of fibrinolysis by injecting 16 mg dexamethasone intraperitoneally in 10 patients 24 h before ascites retransfusion was performed. In addition, the effect of dexamethasone upon the activity or concentration of several proteases and antiproteases related to coagulation in plasma and ascites was analyzed on 15 occasions. An increase of the activity of plasminogen, α2-antiplasmin, and antithrombin III, and in the concentration of α1-protease inhibitor in ascites was induced by the dexamethasone injection. However, the reaction was not identical in all patients. Those patients having an increase of plasminogen activities of 0.6 CTA U/ml or more did not show signs of fibrinolysis during retransfusion. The results obtained indicate that intraperitoneal injection of dexamethasone decreases the concentration of plasminogen activators in ascites and thereby reduces the risk of coagulation disorders during retransfusion procedures. Since the effect is variable and not sustained, assessment of preoperative plasminogen concentrations is mandatory in order to prevent complications.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1440
    Keywords: Plasminogen ; Fibronectin ; Antiproteases ; Ascites ; Liver cirrhosis ; Tumors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The concentrations of several proteases and antiproteases known to be present in ascites were tested in plasma and ascitic fluid with regard to their ability to separate ascites according to malignant or nonmalignant disease. Seventeen patients with proven malignant ascites and 37 with ascites due to liver cirrhosis were included. Activities of plasminogen,α 2-antiplasmin, antithrombin-III, and factor V, and the concentration ofα 1-protease inhibitor were significantly higher in the plasma of patients with malignant ascites than in cirrhotic patients. Fibronectin, plasminogen,α 2-macroglobulin,α 1-protease inhibitor, antithrombin-III, and albumin revealed higher concentrations or activities in malignant ascites than in cirrhotic ascites. Due to a wide variation of most parameters, only fibronectin, antithrombin III, andα 1-protease inhibitor in ascites had a sensitivity and specificity higher than 90% for malignant ascites. When the specific protein/albumin ratio was used, only the accuracy of fibronectin was increased reaching a sensitivity and specificity of 100%. The plasma/ascites gradients of the proteins assessed differed significantly, that of fibronectin being much higher (22±7) than that of all other proteins. In malignant ascites fibronectin concentration was only correlated withα 1-protease inhibitor concentration but not with the concentration or activity of all other proteins, while in cirrhotic ascites most proteins revealed a positive correlation. The determination of the fibronectin concentration or the fibronectin/albumin ratio in ascites can differentiate malignant and nonmalignant ascites. All other proteases and antiproteases assessed are of lesser value for this purpose, although most are significantly increased in ascites and plasma of patients with malignant disorders.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 65 (1987), S. 726-726 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-2451
    Keywords: Burn disease ; Toxin isolation ; Electromycroscopy of the liver ; Immunology ; Verbrennungskrankheit ; Toxinisolierung ; Elektronenmikroskopie der Leber ; Immunologie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: ZusammenfaBung Bei der Verbrennung bilden sich toxische Substanzen in der Haut, die aus tierischer, menschlicher Haut und dem Serum schwerverbrannter Patienten isoliert wurden. Das „Toxin”, ein Lipid-Protein-Komplex, das als Vorstufe in der normalen Haut vorkommt, wirkt im Tierversuch bei i.p. Applikation letal, setzt die Infektionsresistenz herab, wird in allen Organen angereichert und schädigt die Zellen, wie Untersuchungen der Ultrastruktur und des Stoffwechsels der Leber nachwiesen. Ein Antitoxin wurde entwickelt, das im Tierversuch eine signifikante Schutzwirkung zeigte.
    Notes: Summary In high temperature burns a specific substance is formed in the skin that has been isolated from in vitro burned animal and human skin as well as from serum of serverely burned patients. This toxic lipid-protein complex derived from a naturally occurring precursor has a lethal effect when injected i.p. into recepient mice. It accumulates in all organs and reduces the animals' resistance to infection. Cell destruction was shown by ultrastructural and metabolic changes in the liver. An antitoxin was developed that protects against the lethal effect as well as the superimposed sepsis.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 64 (1986), S. 1182-1182 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 1014-1014 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 41-41 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 1043-1043 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 67 (1989), S. 755-755 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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