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  • Spinal Cord  (1)
  • Staphylococcal Toxin  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 262 (1969), S. 165-182 
    ISSN: 1432-1912
    Keywords: Radioimmunassay ; Blood Level ; Staphylococcal Toxin ; Solid Phase ; Antibodies ; Radioimmunassay ; Blutspiegel ; Staphylokokken-Toxin ; Festphase ; Antikörper
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung 1. Es wird ein „solid-phase-radioimmunassay“ unter Verwendung von kovalent an Cellulose gebundenen Antikörpern entwickelt. Vorteile und Reaktionsbedingungen werden am Beispiel des Staphylokokken-α-Toxins dargestellt. 2. Einige der untersuchten Kaninchenseren, Humanplasma und vor allem natives antitoxisches Serum enthalten präcipitierende Antikörper, welche von der zugesetzten Radioaktivität um so mehr binden, je höher die Konzentration an unmarkiertem Toxin ist („inverser“ Radioimmunassay). 3. Unmarkiertes und markiertes Toxin verschwinden ungewöhnlich schnell (Halbwertszeit 〈 5 min) aus dem zirkulierenden Blut des Kaninchens. Eliminiertes markiertes Toxin läßt sich durch Gabe von Antitoxin nicht in die Blutbahn zurückholen. Vorherige Applikation von Normal-Rinderserum und von antitoxischem Rinderserum verzögert die Elimination des α-Toxins. 4. Nach doppelseitiger Nierenligatur wird markiertes Toxin erheblich langsamer aus der Blutbahn eliminiert; Ligatur beider Ureteren ist in dieser Hinsicht weniger effektiv.
    Notes: Summary 1. A solid-phase radioimmunassay has been developed which utilizes antibodies covalently bound to cellulose. Its advantages and reaction conditions have been demonstrated with staphylococcal α-toxin. 2. Sera of some rabbits, human plasma and especially native antitoxic sera contain precipitating antibodies which bind added radioactive toxin in proportion to the concentration of native toxin (“inverse” radioimmunassay). 3. Native and labelled toxins disappear very quickly from the circulating blood of rabbits (half-life time below 5 min). After its disappearance from the blood, radioactive toxin cannot be redistributed into the circulation by injection of antitoxin. Previous injection of normal or antitoxic bovine serum delays the elimination of α-toxin. 4. Previous ligation of both kidneys delays the elimination of labelled toxin from the blood stream considerably. Ligation of the ureters is less effective in this respect.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 276 (1973), S. 361-373 
    ISSN: 1432-1912
    Keywords: Tetanus Toxin ; Iodine Labelling ; Spinal Cord ; Autoradiography ; Antitoxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The in vivo interaction of 125I-labelled toxin with substructures of rat spinal cord has been studied. The rats were poisoned by i.v. injection about 40–50 h before sacrifice. 1. The labelled material accumulates in the grey substance, which is, on microdissection, about 6 times more active than the white. Autoradiography reveals that the toxin is particularly enriched in the ventrolateral part of the grey substance. 2. On ultracentrifugation of the homogenates, the label is preferentially fixed to the dense fractions known to contain the synaptosomes. However, a considerable part of the toxin is fixed to the lighter fractions too. 3. Upon gel filtration, the labelled material in SDS-homogenates from spinal cords poisoned in vivo is indistinguishable from toxin added to the homogenates already prepared. The same is true for the bulk of radioactivity when subjected to disc gel electrophoresis. 4. The labelled material is degraded by enzymes from spinal cord at pH 3.5, but not at pH 7.5. 5. The labelled material is relatively firmly bound to structures of spinal cord. The bonding is fairly resistant against washing, even in the presence of an excess of cold toxin, but it can be partially released by treatment with antitoxin. According to these findings, the labelled material is firmly but not irreversibly bound in vivo to discrete structures, corresponding preferentially to the synaptosomal fractions in the homogenates and the ventrolateral grey in the slices. No evidence has been found for its degradation in vivo. So far, the bulk of labelled material in the spinal cord is indistinguishable from tetanus toxin.
    Type of Medium: Electronic Resource
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