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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 246 (1963), S. 38-39 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 250 (1965), S. 233-234 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 264 (1969), S. 237-238 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 236 (1959), S. 301-301 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 245 (1962), S. 66-67 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 255 (1966), S. 3-3 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 257 (1967), S. 264-265 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 241 (1961), S. 223-224 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 264 (1969), S. 214-215 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-0738
    Keywords: PCB ; Liver microsomes ; Microscopy ; Porphyrins ; Residues
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über Leberveränderungen an Ratten nach subchronischer Fütterung mit 2000 ppm PCB berichtet. Dabei wurden drei Chargen eines technischen Trichlorbiphenyls eingesetzt, die einen unterschiedlichen Gehalt (%) an hochchlorierten Komponenten (d. h.≥5 Cl) hatten, und zwar: 5% =triCB-5; 2% = triCB-2 und 0,4% = triCB-04. Der auffälligste Wirkungsunterschied der Präparate bestand in den porphyrinogenen Eigenschaften. Während triCB-0,4 und triCB-2 einen Anstieg des Porphyringehaltes der Leber um den Faktor 17 bzw. 7 verursachten, stieg der Gehalt nach triCB-5 175fach höher als normal an. Die Porphyrine bestanden hauptsächlich aus Uroporphyrin und Heptacarboxyporphyrin. Im Gegensatz zu den unterschiedlichen porphyrinogenen Wirkungen bewirkten alle drei triCB-Präparate eine gleich hohe Induktion der δ-Aminolaevulinatsynthetase. Die δ-Aminolaevulinatdehydratase erfuhr keine Veränderung ihrer Aktivität. Die mikrosomalen Monoxygenasen und die UDP-Glucuronyltransferase wurden durch alle drei triCB induziert. Die höchsten Werte wurden wieder durch triCB-5 erzielt. Sie korrelieren damit zu den PCB-Rückständen in der Leber, denn nach Fütterung mit triCB-5 kam es zu einer wesentlich höheren Akkumulation der hochchlorierten Komponenten. Bei licht- und elektronenmikroskopischer Untersuchung konnten keine signifikant unterschiedlichen Wirkungen der triCB-Präparate festgestellt werden. Die Lebern aller Tiere zeigten eine erhebliche Zellhypertrophie, die durch die Hyperproliferation des tubulären und vesikulären glatten endoplasmatischen Retikulums hervorgerufen wurde. Die Membranen des Retikulums waren dicht gepackt und manchmal zerrissen. In den meisten Zellen konnten außerdem unterschiedlich große „membrane arrays“ gesehen werden, die zu einer Verdrängung von Mitochondrien führte. Einige Mitochondrien waren geschwollen. Zentrolobuläre oder periportale Nekrosen, Fibrosen oder fettige Degenerationen konnten nicht beobachtet werden. Aus den Untersuchungen kann gefolgert werden, daß PCB-Produkte mit niedrigem Chlorgehalt (42%) wesentlich weniger toxisch sind als solche mit hohem Gehalt. Toxische Effekte können aber dadurch auftreten, daß die in den Handelspräparaten als Verunreinigung enthaltenen hochchlorierten Komponenten akkumulieren.
    Notes: Abstract Liver changes were studied after subchronic feeding a diet containing 2000 ppm PCB [chlorine content 42% corresponding to trichlorobiphenyls (triCB)]. The products differed in their content of highly chlorinated biphenyls (≥Cl5-biphenyl; 5%=triCB-5, 2%=triCB-2 and 0.4%=triCB-0.4). The most striking difference was observed in respect to their porphyrinogenic actions. TriCB-0.4 and triCB-2 caused an increase of porphyrins about 10-fold, whereas the liver porphyrin content of triCB-5 treated rats was 175-fold higher than normal. In all cases of porphyria the porphyrins consisted mainly of uro- and heptacarboxyporphyrin. In contrast to their different porphyrinogenic effects all triCB products caused an equal induction of δ-aminolaevulinate synthetase, but no increase of δ-aminolaevulinate dehydratase activity. TriCB-5 was also a stronger inducer than triCB-0.4 and triCB-2 regarding microsomal monoxygenases and UDP-glucuronyltransferase. The quantitative differences of the effect can be correlated to PCB residues in the liver. In triCB-5 fed rats a much higher accumulation of highly chlorinated components could be determined. The histological examination by light and electron microscopy showed no significant differences in the effects caused by all three triCB products. In livers of all rats cell hypertrophy could be observed due to a considerable hyperproliferation of tubular and vesicular SER. SER membranes were tightly packed and sometimes disrupted. Membrane arrays of various size were found in most hepatocytes. The mitochondria were dislocated by these formations and were sometimes swollen. There was neither centrilobular or periportal necrosis nor fibrosis nor fatty degeneration. It may be concluded that PCB of low chlorine content (42%) are much less toxic than highly chlorinated PCB. However, the small amount of highly chlorinated components, present as contaminants in commercial products containing 42% chlorine, may accumulate and exert toxic effects.
    Type of Medium: Electronic Resource
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